FHIR IG analytics| Package | noma.fhir.mpd |
| Resource Type | CodeSystem |
| Id | Pharmaceutical_Dose_Form.json |
| FHIR Version | R4 |
| Source | https://simplifier.net/resolve?scope=noma.fhir.mpd@2.0.0&canonical=https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8 |
| URL | https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8 |
| Status | active |
| Name | Pharmaceutical Dose Form Examples |
| Content | complete |
No resources found
No resources found
No narrative content found in resource
FHIR
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"code": "200000002080",
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"code": "200000002064",
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},
{
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"code": "200000002052",
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{
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{
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"value": "Pulver til urtete"
},
{
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"value": "pulv til urtete"
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{
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}
],
"property": [
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},
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"code": "200000002073",
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{
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"code": "200000002103",
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"code": "200000002052",
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{
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}
],
"property": [
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"code": "263"
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},
{
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},
{
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"code": "200000002075",
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{
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"code": "200000002086",
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},
{
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"code": "200000002080",
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{
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"code": "200000002064",
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002041",
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},
{
"code": "administrationMethod",
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"code": "200000002052",
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{
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{
"language": "en",
"use": {
"code": "term-description"
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],
"property": [
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"code": "215"
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},
{
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},
{
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},
{
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"code": "200000002075",
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}
},
{
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},
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},
{
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"code": "200000002086",
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},
{
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"code": "200000002077",
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},
{
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"code": "200000002064",
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},
{
"code": "administrationMethod",
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"code": "200000002052",
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},
{
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{
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{
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{
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"value": "Solid preparation consisting of granules showing a rate and/or place of release different from that of conventional-release granules. This deliberate modification is achieved by a special formulation design and/or manufacturing method. Modified-release granules are usually single-dose preparations intended for oral use, and include prolonged-release, delayed release and pulsatile-release granules. The generic term 'modified-release granules' is used only when the more specific terms 'gastro-resistant granules' or 'prolonged-release granules' do not apply."
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],
"property": [
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"code": "internalCode",
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"code": "265"
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},
{
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},
{
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},
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},
{
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"code": "200000002075",
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},
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{
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},
{
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"code": "200000002086",
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},
{
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"code": "200000002079",
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},
{
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"code": "200000002064",
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},
{
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"code": "200000002052",
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{
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],
"property": [
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},
{
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},
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"code": "200000002075",
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},
{
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{
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"code": "200000002084",
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},
{
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"code": "200000002080",
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
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},
{
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{
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"value": "Solid single-dose, delayed-release preparation contained in a hard shell. The preparation is intended to resist the gastric fluid and to release the active substance(s) in the intestinal fluid. Hard gastro-resistant capsules are usually made by filling hard capsules with gastro-resistant granules or solid particles made gastro-resistant by coating or, in certain cases, by providing hard capsules with a gastro-resistant shell. They are intended for oral use."
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],
"property": [
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{
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"code": "200000002084",
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},
{
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"code": "200000002077",
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{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
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},
{
"code": "100000073377",
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"language": "en",
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{
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{
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{
"language": "en",
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"value": "Solid single-dose preparation contained in a soft shell. The soft capsule is intended to be chewed to release its contents into the mouth. The contents of the soft shell may be a semi-solid or liquid preparation intended for local action or systemic delivery after absorption through the oral mucosa or, when swallowed, in the gastrointestinal tract."
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],
"property": [
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"display": "Current"
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"code": "200000002075",
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{
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{
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"code": "200000002084",
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},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
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{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
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{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002041",
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{
"code": "administrationMethod",
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},
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},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
"display": "Oromucosal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002041",
"display": "Chewing"
}
}
]
},
{
"code": "100000073670",
"display": "Pillules",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Pillules"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Granuler"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "granuler"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation for homoeopathic use, obtained from sucrose, lactose or other suitable excipients. Pillules may be prepared by impregnation of preformed pillules with a dilution or dilutions of homoeopathic stocks or by progressive addition of these excipients and the addition of a dilution or dilutions of homoeopathic stocks. Pillules are intended for oral or sublingual use."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "271"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073670"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
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}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002097",
"display": "Pillules"
}
},
{
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"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000032311",
"display": "Sublingual"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
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}
]
},
{
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"language": "en",
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"code": "term-name"
},
"value": "Gargle"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Gurglevann"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "gurglevann"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of an aqueous solution intended for gargling to obtain a local effect in the oral cavity and the throat. Gargles are not to be swallowed."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "274"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073673"
}
},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
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}
},
{
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
"display": "Oromucosal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002042",
"display": "Gargling"
}
}
]
},
{
"code": "100000073674",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Gargle, powder for solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til gurglevann, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til gurglevann oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of one or more powders intended to be dissolved in water to obtain a gargle."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1342"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073674"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
"display": "Oromucosal"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002042",
"display": "Gargling"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073673",
"display": "Gargle"
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}
]
},
{
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},
"value": "Oromucosal suspension"
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{
"language": "no",
"use": {
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},
"value": "Munnvann, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "munnvann susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid single-dose or multidose preparation consisting of a suspension intended for oromucosal use."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1047"
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},
{
"code": "termIdRms",
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"code": "100000073675"
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},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
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}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
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}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002009",
"display": "Suspension"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
"display": "Oromucosal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
"code": "100000073677",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Mouthwash"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Munnskyllevæske"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "munnskyllevæske"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of an aqueous solution intended for use in contact with the oral mucosa. It is not to be swallowed. Mouthwashes may contain excipients to adjust the pH which as far as possible is neutral."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1044"
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},
{
"code": "termIdRms",
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"code": "100000073677"
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},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
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}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
"display": "Oromucosal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002049",
"display": "Rinsing/washing"
}
}
]
},
{
"code": "100000073678",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Gingival solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Oppløsning til tannkjøtt"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "oppl til tannkjøtt"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid, usually multidose preparation consisting of a solution intended for gingival use."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1191"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073678"
}
},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
"display": "Oromucosal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
"code": "100000073679",
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"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Oromucosal paste"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Munnpasta"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "munnpasta"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Semi-solid single-dose or multidose preparation consisting of a paste of solid particles finely dispersed in a hydrophilic basis intended for oromucosal use. Oromucosal pastes are applied to the oral cavity or onto a specific part of the oral cavity, to obtain a local effect. Gingival paste is excluded."
}
],
"property": [
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"code": "internalCode",
"valueCoding": {
"code": "1042"
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},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073679"
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},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
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},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002037",
"display": "Paste"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
"display": "Oromucosal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
"code": "100000073680",
"display": "Gingival gel",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Gingival gel"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Gel til tannkjøtt"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "gel til tannkjøtt"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Semi-solid single-dose or multidose preparation consisting of a gel intended for gingival use to obtain a local effect."
}
],
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},
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},
{
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{
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{
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{
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},
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],
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},
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},
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],
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},
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},
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},
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"code": "200000002106",
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},
{
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"code": "200000002080",
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},
{
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},
{
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{
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],
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},
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},
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"code": "200000002104",
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},
{
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{
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},
{
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{
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],
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},
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"code": "200000002037",
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},
{
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{
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{
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{
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],
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},
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"code": "200000002080",
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{
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
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{
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{
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"value": "bukkaltab"
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{
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"value": "Solid single-dose preparation to be applied to the buccal cavity (pouch) to obtain systemic delivery. Buccal tablets are prepared by compression of mixtures of powders or granulations into tablets with a shape suited for the intended use."
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],
"property": [
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"code": "55"
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},
{
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},
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},
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"code": "200000002075",
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},
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{
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"code": "200000002102",
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},
{
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"code": "200000002080",
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{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000032310",
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
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},
{
"code": "100000073700",
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"value": "Compressed lozenge"
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{
"language": "no",
"use": {
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"value": "Sugetablett, komprimert"
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{
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"value": "sugetab"
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{
"language": "en",
"use": {
"code": "term-description"
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"value": "Solid single-dose preparation intended to be sucked to obtain a local or systemic effect. It is prepared by compression and is often rhomboid in shape. Compressed lozenges usually contain flavouring and sweetening agents. They dissolve or disintegrate slowly when sucked."
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],
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}
],
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},
{
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{
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],
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},
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},
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},
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},
{
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{
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],
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},
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},
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},
{
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{
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{
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{
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],
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},
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},
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},
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},
{
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},
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},
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"code": "200000002104",
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},
{
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{
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},
{
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},
{
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],
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},
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"code": "200000002107",
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},
{
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"code": "200000002080",
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},
{
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{
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},
{
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"code": "200000002039",
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},
{
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{
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}
],
"property": [
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},
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},
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},
{
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},
{
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"code": "200000002075",
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},
{
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},
{
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{
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"code": "200000002098",
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},
{
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{
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{
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"value": "Liquid or, occasionally, semi-solid, usually multidose preparation intended for application to the scalp by rubbing and subsequent washing away with water. Upon rubbing with water, shampoos usually form foam. Shampoos are solutions, suspensions or emulsions containing surface-active agents."
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],
"property": [
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"code": "1436"
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},
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},
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},
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},
{
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"code": "200000002075",
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},
{
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},
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002017",
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},
{
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"code": "200000002080",
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{
"code": "intendedSite",
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{
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"code": "200000002039",
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{
"code": "100000073716",
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"use": {
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},
{
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"use": {
"code": "short-name"
},
"value": "hudspray, susp"
},
{
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}
],
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"code": "300"
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},
{
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},
{
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},
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},
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{
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}
},
{
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{
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},
{
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},
{
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{
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{
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},
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}
],
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},
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},
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},
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}
},
{
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{
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}
},
{
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{
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},
{
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{
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},
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{
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{
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},
{
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},
"value": "Liquid preparation intended to be diluted in the specified liquid to obtain a cutaneous solution."
}
],
"property": [
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"code": "956"
}
},
{
"code": "termIdRms",
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},
{
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},
{
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},
{
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"code": "200000002071",
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}
},
{
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},
{
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"code": "200000002002",
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}
},
{
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}
},
{
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}
},
{
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"code": "200000002039",
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}
},
{
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}
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},
{
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{
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}
],
"property": [
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},
{
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},
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},
{
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},
{
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}
},
{
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},
{
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}
},
{
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"code": "200000002004",
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}
},
{
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}
},
{
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},
{
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}
]
},
{
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},
{
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"use": {
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{
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],
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"code": "1975"
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},
{
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},
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},
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},
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}
},
{
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},
{
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{
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}
},
{
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}
},
{
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},
{
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}
]
},
{
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{
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{
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{
"language": "en",
"use": {
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},
"value": "Solid preparation consisting of one or more powders intended for administration within the tooth socket/periodontal membrane."
}
],
"property": [
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"code": "79"
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},
{
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},
{
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},
{
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},
{
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"code": "200000002075",
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}
},
{
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},
{
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}
},
{
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"code": "200000002099",
"display": "Powder"
}
},
{
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},
{
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"code": "200000002056",
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}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
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}
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},
{
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"value": "Dental stick"
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{
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"use": {
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{
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{
"language": "en",
"use": {
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"value": "Solid single-dose preparation, rod-shaped and usually prepared by compression or moulding, intended for dental use."
}
],
"property": [
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"code": "68"
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},
{
"code": "termIdRms",
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},
{
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},
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},
{
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},
{
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{
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"code": "200000002100",
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}
},
{
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"code": "200000002080",
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},
{
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"code": "200000002056",
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
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},
{
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"use": {
"code": "term-name"
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"value": "Dental solution"
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{
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"use": {
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"value": "Dentalvæske, oppløsning"
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{
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"use": {
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"value": "dentalvæske, oppl"
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{
"language": "en",
"use": {
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"value": "Liquid, usually multidose preparation consisting of a solution intended for administration on teeth and gums."
}
],
"property": [
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"valueCoding": {
"code": "73"
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},
{
"code": "termIdRms",
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"code": "100000073723"
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},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
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},
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"display": "Current"
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},
{
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"code": "200000002075",
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}
},
{
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},
{
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},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
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},
{
"code": "releaseCharacteristics",
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"code": "200000002080",
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{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002056",
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}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
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}
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{
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}
],
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},
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},
{
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],
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},
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],
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},
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},
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},
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},
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],
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"code": "200000002007",
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},
{
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},
{
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{
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],
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{
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
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}
]
},
{
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{
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"code": "term-name"
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"value": "Cutaneous suspension"
},
{
"language": "no",
"use": {
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},
{
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},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid, usually multidose preparation consisting of a suspension of fine particles in a suitable vehicle intended for cutaneous use."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "984"
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},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073732"
}
},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
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},
{
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"code": "200000002075",
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}
},
{
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"code": "MANUFACTURED",
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},
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}
},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002009",
"display": "Suspension"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
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}
]
},
{
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{
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"use": {
"code": "term-name"
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"value": "Pudder"
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{
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},
{
"language": "en",
"use": {
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},
"value": "Solid, usually multidose preparation consisting of a powder intended for cutaneous use. Cutaneous spray, powder is excluded."
}
],
"property": [
{
"code": "internalCode",
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"code": "1295"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073733"
}
},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002075",
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}
},
{
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},
{
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"code": "200000002099",
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}
},
{
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"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"code": "200000002055",
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}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
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}
]
},
{
"code": "100000073734",
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"language": "en",
"use": {
"code": "term-name"
},
"value": "Solution for iontophoresis"
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{
"language": "no",
"use": {
"code": "term-name"
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"value": "Iontoforeseoppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "iontoforeseoppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of an aqueous solution intended for transdermal delivery by means of iontophoresis."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "840"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073734"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
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}
},
{
"code": "manufacturedAndOrAdministrable",
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}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000032309",
"display": "Transdermal"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
"code": "100000073735",
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{
"language": "en",
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"code": "term-name"
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"value": "Collodion"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Kollodium"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "kollodium"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation usually containing pyroxylin in a mixture of ether and ethanol. When applied to the skin, the preparation forms a flexible film on the site of application."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "931"
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},
{
"code": "termIdRms",
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"code": "100000073735"
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},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
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}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002075",
"display": "No transformation",
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}
},
{
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"code": "MANUFACTURED",
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}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002001",
"display": "Collodion"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
"code": "100000073736",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Poultice"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Omslag"
},
{
"language": "no",
"use": {
"code": "short-name"
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"value": "omslag"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Semi-solid preparation consisting of a hydrophilic heat-retentive basis in which solid or liquid active substance(s) are dispersed, usually intended to be spread thickly on a suitable dressing and heated before application to the skin."
}
],
"property": [
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"code": "internalCode",
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"code": "1105"
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},
{
"code": "termIdRms",
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"code": "100000073736"
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},
{
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"code": "Godkjent SPOR",
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}
},
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"display": "Current"
}
},
{
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"code": "200000002075",
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}
},
{
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002000",
"display": "Poultice"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000032309",
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}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
"code": "100000073741",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Transdermal patch"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Depotplaster"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "depotplaster"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Flexible single-dose preparation intended to be applied to the unbroken skin to obtain a systemic delivery over an extended period of time. Transdermal patches consist of a backing sheet supporting a reservoir or a matrix containing the active substance(s) and on the top a pressure-sensitive adhesive, which assures the adhesion of the preparation to the skin. The backing sheet is impermeable to the active substance(s) and normally impermeable to water. In reservoir systems the active substance may be dissolved or dispersed in a semi-solid basis or in a solid polymer matrix, which is separated from the skin by a rate-controlling membrane. The pressure-sensitive adhesive may, in this case, be applied to some or all parts of the membrane, or only around the border of the membrane and the backing sheet. Matrix systems contain the active substance in a solid or semi-solid matrix, the properties of which control the diffusion pattern to the skin. The matrix system may also be a solution or dispersion of the active substance in the pressure-sensitive adhesive. The releasing surface of the patch is covered by a protective liner to be removed before applying the patch to the skin."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "101"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073741"
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},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
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}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002094",
"display": "Patch"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000032309",
"display": "Transdermal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
"code": "100000073742",
"display": "Medicated nail lacquer",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Medicated nail lacquer"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Medisinsk neglelakk"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "medisinsk neglelakk"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation to be applied to the nails to form a lacquer by evaporation of the volatile solvent."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1014"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073742"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002005",
"display": "Lacquer"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
"code": "100000073743",
"display": "Cutaneous stick",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Cutaneous stick"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Hudstift"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "hudstift"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation, usually rod-shaped or conical, intended for application to the skin to obtain a local effect. Cutaneous sticks may consist of the active substance(s) alone or dissolved or dispersed in a suitable basis."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "301"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073743"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002075",
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}
},
{
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}
},
{
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}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002100",
"display": "Stick"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
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}
]
},
{
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{
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},
"value": "Impregnated dressing"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Impregnert kompress"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "impreg kompress"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of a piece or strip of gauze or other suitable fabric impregnated with a liquid or semi-solid preparation intended for cutaneous use."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "315"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073744"
}
},
{
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
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"code": "MANUFACTURED",
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}
},
{
"code": "manufacturedAndOrAdministrable",
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}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002089",
"display": "Impregnated material"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
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}
]
},
{
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},
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},
{
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"value": "Oppløsning til prikktest"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "oppl til prikktest"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a solution containing an allergen product intended for diagnostic use in a skin-prick test."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1189"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073756"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
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}
},
{
"code": "manufacturedAndOrAdministrable",
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}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
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"language": "en",
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},
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},
{
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"value": "Plaster til provokasjonstest"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "plaster til provok test"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid flexible preparation containing an allergen product intended for provocation testing by application to the skin."
}
],
"property": [
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"code": "internalCode",
"valueCoding": {
"code": "1792"
}
},
{
"code": "termIdRms",
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}
},
{
"code": "internalTermStatus",
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}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
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}
},
{
"code": "manufacturedAndOrAdministrable",
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}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002098",
"display": "Plaster"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
"code": "100000073758",
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"language": "en",
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"code": "term-name"
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"value": "Eye gel"
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{
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"value": "Øyegel"
},
{
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"use": {
"code": "short-name"
},
"value": "øyegel"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Semi-solid sterile single-dose or multidose preparation consisting of a gel intended for ocular use. Eye gels may be presented in collapsible tubes fitted with a cannula and having a content of not more than 5 g of the preparation. Eye gels may also be presented in suitably designed single-dose containers. The containers or nozzles of tubes are of a shape that facilitates administration without contamination."
}
],
"property": [
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"code": "1766"
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},
{
"code": "termIdRms",
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},
{
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002075",
"display": "No transformation",
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}
},
{
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"code": "MANUFACTURED",
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}
},
{
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"display": "administrable"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002106",
"display": "Gel"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002063",
"display": "Ocular"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
"code": "100000073759",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Eye drops, solution"
},
{
"language": "no",
"use": {
"code": "term-name"
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"value": "Øyedråper, oppløsning"
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{
"language": "no",
"use": {
"code": "short-name"
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"value": "øyedr, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile single-dose or multidose preparation consisting of an aqueous or oily solution intended for ocular use. Multidose preparations are presented in containers that allow successive drops to be administered. The containers contain usually at most 10 mL of the preparation."
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],
"property": [
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"code": "1759"
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},
{
"code": "termIdRms",
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"code": "100000073759"
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},
{
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
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},
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"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002063",
"display": "Ocular"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002047",
"display": "Instillation"
}
}
]
},
{
"code": "100000073760",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Eye drops, suspension"
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{
"language": "no",
"use": {
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"value": "Øyedråper, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "øyedr, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile single-dose or multidose preparation consisting of an aqueous or oily suspension intended for ocular use. Multidose preparations are presented in containers that allow successive drops to be administered. The containers contain usually at most 10 mL of the preparation."
}
],
"property": [
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"code": "internalCode",
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"code": "1764"
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},
{
"code": "termIdRms",
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"code": "100000073760"
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},
{
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002009",
"display": "Suspension"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002063",
"display": "Ocular"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002047",
"display": "Instillation"
}
}
]
},
{
"code": "100000073769",
"display": "Transdermal system",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Transdermal system"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Transdermalt system"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "transdermalt system"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Assembly of components intended for transdermal delivery driven by external forces (e.g. electric current, chemical reaction,...). Transdermal patch is excluded."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1775"
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},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073769"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002019",
"display": "System"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000032309",
"display": "Transdermal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
"code": "100000073770",
"display": "Solution for skin-scratch test",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Solution for skin-scratch test"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Oppløsning til risptest"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "oppl til risptest"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a solution containing an allergen product intended for diagnostic use in a skin-scratch test."
}
],
"property": [
{
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"code": "1791"
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},
{
"code": "termIdRms",
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"code": "100000073770"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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},
{
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},
{
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"code": "200000002007",
"display": "Solution"
}
},
{
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"code": "200000002080",
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}
},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
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}
]
},
{
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{
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{
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},
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}
],
"property": [
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},
{
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},
{
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},
{
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"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002075",
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}
},
{
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},
{
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},
{
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"code": "200000002104",
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}
},
{
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"code": "200000002080",
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},
{
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"code": "200000002063",
"display": "Ocular"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
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}
]
},
{
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{
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{
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"value": "øyesalve"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Semi-solid sterile single-dose or multidose preparation consisting of an ointment intended for ocular use. Eye ointments may be presented in collapsible tubes fitted with a cannula and having a content of not more than 5 g of the preparation. Eye ointments may also be presented in suitably designed single-dose containers. The containers or nozzles of tubes are of a shape that facilitates administration without contamination."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1770"
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},
{
"code": "termIdRms",
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"code": "100000073772"
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},
{
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"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
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}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
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},
{
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"code": "ADMINISTRABLE",
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}
},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002107",
"display": "Ointment"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002063",
"display": "Ocular"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
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}
]
},
{
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{
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{
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{
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"use": {
"code": "term-description"
},
"value": "Liquid sterile single-dose or multidose preparation consisting of an emulsion intended for ocular use. Multidose preparations are presented in containers that allow successive drops to be administered. The containers contain usually at most 10 mL of the preparation."
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],
"property": [
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"code": "3"
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},
{
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},
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},
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"display": "Current"
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},
{
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"code": "200000002075",
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}
},
{
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},
{
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002004",
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}
},
{
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}
},
{
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"code": "200000002063",
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}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002047",
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}
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},
{
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{
"language": "en",
"use": {
"code": "term-name"
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"value": "Eye drops, solvent for reconstitution"
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{
"language": "no",
"use": {
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{
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"value": "rekonst væske til øyedr"
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{
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"use": {
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"value": "Liquid preparation consisting of a sterile solvent containing no active substances, intended for reconstitution of a usually freeze-dried powder for eye drops."
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],
"property": [
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"code": "1397"
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},
{
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},
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},
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},
{
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"code": "200000002074",
"display": "Mixing",
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}
},
{
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002008",
"display": "Solvent"
}
},
{
"code": "releaseCharacteristics",
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"code": "200000002080",
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},
{
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"code": "200000002063",
"display": "Ocular"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002047",
"display": "Instillation"
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}
]
},
{
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{
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"value": "Eye lotion"
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{
"language": "no",
"use": {
"code": "term-name"
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"value": "Øyebadevann"
},
{
"language": "no",
"use": {
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"value": "Øyebadevann"
},
{
"language": "en",
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"value": "Liquid sterile single-dose or multidose preparation consisting of an aqueous solution intended for washing or bathing the eye."
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],
"property": [
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},
{
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},
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},
{
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},
{
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"code": "200000002075",
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}
},
{
"code": "manufacturedAndOrAdministrable",
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},
{
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},
{
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"code": "200000002007",
"display": "Solution"
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},
{
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"code": "200000002080",
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}
},
{
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002040",
"display": "Bathing"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002049",
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}
]
},
{
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{
"language": "en",
"use": {
"code": "term-name"
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"value": "Ophthalmic insert"
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{
"language": "no",
"use": {
"code": "term-name"
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"value": "Øyelamell"
},
{
"language": "no",
"use": {
"code": "short-name"
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"value": "øyelamell"
},
{
"language": "en",
"use": {
"code": "term-description"
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"value": "Solid sterile preparation of suitable size and shape, designed to be inserted in the conjunctival sac to produce a local or ocular effect by the release of active substance(s) over a determined period of time. Ophthalmic inserts generally consist of a reservoir of active substance(s) embedded in a matrix or bounded by a rate-controlling membrane. They are presented individually in sterile containers."
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],
"property": [
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"code": "internalCode",
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},
{
"code": "termIdRms",
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"code": "100000073777"
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},
{
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},
{
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"display": "Current"
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},
{
"code": "transformation",
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"code": "200000002075",
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}
},
{
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}
},
{
"code": "manufacturedAndOrAdministrable",
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002012",
"display": "Insert"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002063",
"display": "Ocular"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002046",
"display": "Insertion"
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}
]
},
{
"code": "100000073778",
"display": "Ear cream",
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{
"language": "en",
"use": {
"code": "term-name"
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"value": "Ear cream"
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{
"language": "no",
"use": {
"code": "term-name"
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"value": "Ørekrem"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "Ørekrem"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Semi-solid single-dose or multidose preparation consisting of a cream intended for application to the external auditory meatus, if necessary by means of a tampon impregnated with the preparation."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1705"
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},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073778"
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},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
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},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
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},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
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"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
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}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002104",
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}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
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}
},
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},
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],
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},
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"value": "Liquid single-dose or multidose preparation consisting of an emulsion intended for nasal use by means of a suitable applicator."
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],
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"code": "200000002004",
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"code": "200000002047",
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{
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"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002107",
"display": "Ointment"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002069",
"display": "Vaginal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
"code": "100000073813",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Vaginal solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Vaginalvæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "vag væske, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of a solution intended for vaginal use by means of a suitable applicator in order to obtain a local effect."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1670"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073813"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002069",
"display": "Vaginal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
}
]
},
{
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{
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},
"value": "Vaginal emulsion"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Vaginalvæske, emulsjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "vag væske, emul"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of an emulsion intended for vaginal use by means of a suitable applicator in order to obtain a local effect."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1669"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073814"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002004",
"display": "Emulsion"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002069",
"display": "Vaginal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
}
]
},
{
"code": "100000073815",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Pessary"
},
{
"language": "no",
"use": {
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},
"value": "Vagitorie"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "vagitorie"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid, single-dose preparation usually prepared by moulding, of various shapes, usually ovoid, with a volume and consistency suitable for insertion into the vagina to obtain a local effect. It contains one or more active substances dispersed or dissolved in a suitable basis that may be soluble or dispersible in water or may melt at body temperature."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1672"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073815"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
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}
},
{
"code": "manufacturedAndOrAdministrable",
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"display": "administrable"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002096",
"display": "Pessary"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002069",
"display": "Vaginal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002046",
"display": "Insertion"
}
}
]
},
{
"code": "100000073816",
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{
"language": "en",
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},
"value": "Vaginal capsule, soft"
},
{
"language": "no",
"use": {
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},
"value": "Vaginalkapsel, myk"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "vag kaps"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid single-dose preparation consisting of a soft capsule of a size and shape suited for vaginal use, containing a liquid or semi-solid formulation, intended for a local effect."
}
],
"property": [
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"code": "internalCode",
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"code": "1663"
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},
{
"code": "termIdRms",
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"code": "100000073816"
}
},
{
"code": "internalTermStatus",
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"display": "Godkjent SPOR"
}
},
{
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"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
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"display": "manufactured"
}
},
{
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"display": "administrable"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002084",
"display": "Capsule"
}
},
{
"code": "releaseCharacteristics",
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"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002069",
"display": "Vaginal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002046",
"display": "Insertion"
}
}
]
},
{
"code": "100000073817",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Effervescent vaginal tablet"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Vaginalbrusetablett"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "vag brusetab"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid single-dose preparation consisting of a vaginal tablet usually containing acid substances and carbonates or hydrogen carbonates that react rapidly in the presence of aqueous liquid to release carbon dioxide."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1659"
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},
{
"code": "termIdRms",
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"code": "100000073817"
}
},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002102",
"display": "Tablet"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002069",
"display": "Vaginal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002046",
"display": "Insertion"
}
}
]
},
{
"code": "100000073818",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Vaginal delivery system"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Vaginalinnlegg"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "vag innlegg"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Drug delivery system intended to be inserted in the vagina where it releases its contents over an extended period of time. Medicated sponge and medicated vaginal tampon are excluded."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1661"
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},
{
"code": "termIdRms",
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"code": "100000073818"
}
},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
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"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
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"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002019",
"display": "System"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002069",
"display": "Vaginal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002046",
"display": "Insertion"
}
}
]
},
{
"code": "100000073819",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Rectal cream"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Rektalkrem"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "rektalkrem"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Semi-solid preparation consisting of a cream usually presented in a single-dose container provided with a suitable applicator, intended for rectal use to obtain a local effect."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1400"
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},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073819"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002104",
"display": "Cream"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002068",
"display": "Rectal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
}
]
},
{
"code": "100000073820",
"display": "Rectal foam",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Rectal foam"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Rektalskum"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "rektalskum"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation, usually presented in a pressurised container provided with an applicator suitable for delivery to the rectum of foam containing large volumes of gas dispersed in a liquid containing the active substance. Rectal foams are intended for a local effect."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1402"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073820"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
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{
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},
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},
{
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},
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],
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},
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],
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{
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},
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},
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},
{
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},
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},
{
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},
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{
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},
{
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},
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{
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{
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},
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],
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},
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},
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],
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},
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},
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],
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},
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},
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},
{
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},
{
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},
{
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],
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},
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},
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},
{
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},
{
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},
{
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],
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},
{
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{
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},
{
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{
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{
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],
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},
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},
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},
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"code": "200000002002",
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},
{
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},
{
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},
{
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{
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"code": "100000073829",
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}
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{
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{
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{
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],
"property": [
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},
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{
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},
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"code": "200000002101",
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},
{
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"code": "200000002080",
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},
{
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"code": "200000002068",
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002046",
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{
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"language": "en",
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{
"language": "no",
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"value": "Rektalkapsel"
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{
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"value": "rektalkaps"
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{
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"value": "Solid single-dose preparation consisting of a soft capsule of elongated shape suitable for rectal use, containing a liquid or semi-solid formulation, and which may have a lubricating coating."
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],
"property": [
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{
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},
{
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"display": "Godkjent SPOR"
}
},
{
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"display": "Current"
}
},
{
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},
{
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{
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"code": "200000002084",
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}
},
{
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"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
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}
},
{
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},
{
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{
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{
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"use": {
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},
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},
{
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"use": {
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},
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}
],
"property": [
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},
{
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},
{
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},
{
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},
{
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"code": "200000002075",
"display": "No transformation",
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}
},
{
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},
{
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}
},
{
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"code": "200000002089",
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}
},
{
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}
},
{
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"code": "200000002068",
"display": "Rectal"
}
},
{
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}
]
},
{
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{
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{
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},
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},
{
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},
"value": "Liquid preparation consisting of a suspension intended for inhalation use. The suspension is converted into an aerosol by a continuously operating nebuliser or a metered-dose nebuliser."
}
],
"property": [
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"code": "internalCode",
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"code": "463"
}
},
{
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},
{
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},
{
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},
{
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}
},
{
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},
{
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{
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}
},
{
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{
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}
},
{
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},
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],
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},
{
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},
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},
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},
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}
},
{
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}
},
{
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},
{
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},
{
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},
{
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}
},
{
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}
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{
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{
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}
],
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},
{
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},
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},
{
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}
},
{
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},
{
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},
{
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},
{
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}
},
{
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},
{
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{
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{
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],
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},
{
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},
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},
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}
},
{
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},
{
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},
{
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"code": "200000002004",
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}
},
{
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},
{
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},
{
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}
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},
{
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{
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{
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},
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],
"property": [
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},
{
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},
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},
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},
{
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}
},
{
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},
{
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},
{
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},
{
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},
{
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},
{
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{
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"language": "en",
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{
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"use": {
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{
"language": "no",
"use": {
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"value": "pulv til inh damp"
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{
"language": "en",
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"code": "term-description"
},
"value": "Solid preparation consisting of one or more powders of solid active substance(s) intended for generation of vapour to be inhaled to obtain a local effect. The vapour is usually generated by adding the powder to hot water."
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],
"property": [
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},
{
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},
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},
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"code": "200000002074",
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},
{
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"code": "200000002075",
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},
{
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},
{
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"code": "200000002099",
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},
{
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{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002067",
"display": "Pulmonary"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002044",
"display": "Inhalation"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/fca77bf0-11be-4c33-970e-735453b9da1c",
"code": "2289",
"display": "Inhalation vapour"
}
}
]
},
{
"code": "100000073852",
"display": "Inhalation vapour, capsule",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Inhalation vapour, capsule"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Kapsel til inhalasjonsdamp"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "kaps til inh damp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of a capsule formulation intended for generation of vapour to be inhaled to obtain a local effect. The vapour is usually generated by adding the whole capsule or the capsule contents to hot water."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "848"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073852"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002084",
"display": "Capsule"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002067",
"display": "Pulmonary"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002044",
"display": "Inhalation"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/fca77bf0-11be-4c33-970e-735453b9da1c",
"code": "2289",
"display": "Inhalation vapour"
}
}
]
},
{
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"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Inhalation vapour, tablet"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Tablett til inhalasjonsdamp"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "tab til inh damp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of a tablet intended for generation of vapour to be inhaled to obtain a local effect. The vapour is usually generated by adding the tablet to hot water."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1591"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073853"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002102",
"display": "Tablet"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002067",
"display": "Pulmonary"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002044",
"display": "Inhalation"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/fca77bf0-11be-4c33-970e-735453b9da1c",
"code": "2289",
"display": "Inhalation vapour"
}
}
]
},
{
"code": "100000073854",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Inhalation vapour, liquid"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Væske til inhalasjonsdamp"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "væske til inh damp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of a liquid active substance per se, such as an essential oil or a volatile anaesthetic, intended for generation of vapour to be inhaled. The vapour may be generated by adding the liquid to hot water or by the use of a vaporising device."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1690"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073854"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002006",
"display": "Liquid"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002067",
"display": "Pulmonary"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002044",
"display": "Inhalation"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/fca77bf0-11be-4c33-970e-735453b9da1c",
"code": "2289",
"display": "Inhalation vapour"
}
}
]
},
{
"code": "100000073856",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Emulsion for injection"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Injeksjonsvæske, emulsjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "inj, emul"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile single-dose or multidose preparation consisting of an emulsion intended for administration by injection."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "778"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073856"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002004",
"display": "Emulsion"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
}
]
},
{
"code": "100000073857",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Concentrate for solution for injection"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Konsentrat til injeksjonsvæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "kons til inj oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation intended to be diluted in the specified liquid to obtain a solution for injection."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "954"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073857"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002071",
"display": "Dilution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002002",
"display": "Concentrate"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073863",
"display": "Solution for injection"
}
}
]
},
{
"code": "100000073858",
"display": "Emulsion for infusion",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Emulsion for infusion"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Infusjonsvæske, emulsjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "inf, emul"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of an oil-in-water emulsion intended to be introduced, usually in large volumes, usually into the circulating blood stream."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "409"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073858"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002004",
"display": "Emulsion"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002043",
"display": "Infusion"
}
}
]
},
{
"code": "100000073859",
"display": "Powder for solution for infusion",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for solution for infusion"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til infusjonsvæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til inf væske oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified aqueous liquid to obtain a solution for infusion."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1343"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073859"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002043",
"display": "Infusion"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073870",
"display": "Solution for infusion"
}
}
]
},
{
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Inhalation vapour, solution"
},
{
"language": "no",
"use": {
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},
"value": "Oppløsning til inhalasjonsdamp"
},
{
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"use": {
"code": "short-name"
},
"value": "oppl til inh damp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of a solution intended for generation of vapour to be inhaled to obtain a local effect. The vapour is usually generated by adding the solution to hot water."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1183"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073861"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002067",
"display": "Pulmonary"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002044",
"display": "Inhalation"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/fca77bf0-11be-4c33-970e-735453b9da1c",
"code": "2289",
"display": "Inhalation vapour"
}
}
]
},
{
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{
"language": "en",
"use": {
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},
"value": "Inhalation vapour, ointment"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Salve til inhalasjonsdamp"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "salve til inh damp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Semi-solid preparation consisting of an ointment intended for generation of vapour to be inhaled to obtain a local effect. The vapour may be generated by adding the ointment to hot water."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1424"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073862"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002107",
"display": "Ointment"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002067",
"display": "Pulmonary"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002044",
"display": "Inhalation"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/fca77bf0-11be-4c33-970e-735453b9da1c",
"code": "2289",
"display": "Inhalation vapour"
}
}
]
},
{
"code": "100000073863",
"display": "Solution for injection",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Solution for injection"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Injeksjonsvæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "inj, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile single-dose or multidose preparation consisting of a solution intended for administration by injection."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "781"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073863"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
}
]
},
{
"code": "100000073864",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Suspension for injection"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Injeksjonsvæske, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "inj væske, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile single-dose or multidose preparation consisting of a suspension intended for administration by injection."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "791"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073864"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002009",
"display": "Suspension"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
}
]
},
{
"code": "100000073865",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Gel for injection"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Gel til injeksjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "inj gel"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Sterile single-dose preparation consisting of a hydrophilic gel intended for injection into a specific tissue or organ."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "86"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073865"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002106",
"display": "Gel"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
}
]
},
{
"code": "100000073866",
"display": "Powder for solution for injection",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for solution for injection"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til injeksjonsvæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til inj væske, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified liquid to obtain a solution for injection."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1350"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073866"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073863",
"display": "Solution for injection"
}
}
]
},
{
"code": "100000073867",
"display": "Powder for suspension for injection",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for suspension for injection"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til injeksjonsvæske, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til inj væske, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dispersed in the specified liquid to obtain a suspension for injection."
}
],
"property": [
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"code": "internalCode",
"valueCoding": {
"code": "1351"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073867"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073864",
"display": "Suspension for injection"
}
}
]
},
{
"code": "100000073870",
"display": "Solution for infusion",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Solution for infusion"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Infusjonsvæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "inf, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of an aqueous solution intended to be introduced, usually in large volumes, usually into the circulating blood stream."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "412"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073870"
}
},
{
"code": "internalTermStatus",
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},
{
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}
},
{
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},
{
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{
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],
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{
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"value": "hemodiafilt væske"
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{
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},
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{
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{
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"code": "200000002080",
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{
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"code": "200000002058",
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},
{
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"code": "200000002066",
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},
{
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{
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{
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{
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],
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},
{
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},
{
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"code": "200000002002",
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{
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"code": "200000002080",
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{
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073886",
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{
"code": "100000073879",
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"language": "en",
"use": {
"code": "term-name"
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"value": "Bladder irrigation"
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{
"language": "no",
"use": {
"code": "term-name"
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"value": "Blæreskyllevæske"
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{
"language": "no",
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"value": "blæreskyllevæske"
},
{
"language": "en",
"use": {
"code": "term-description"
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"value": "Sterile liquid preparation consisting of sterilised water or an aqueous solution intended for irrigation of the urinary bladder."
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],
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"code": "37"
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},
{
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},
{
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"code": "200000002007",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002061",
"display": "Intravesical"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002049",
"display": "Rinsing/washing"
}
}
]
},
{
"code": "100000073880",
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{
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"code": "term-name"
},
"value": "Urethral gel"
},
{
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"use": {
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},
"value": "Urethralgel"
},
{
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"use": {
"code": "short-name"
},
"value": "urethralgel"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Semi-solid preparation consisting of a gel intended for urethral use by means of a suitable applicator."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1647"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073880"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
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}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002106",
"display": "Gel"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000032312",
"display": "Urethral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
}
]
},
{
"code": "100000073881",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Solvent for parenteral use"
},
{
"language": "no",
"use": {
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},
"value": "Oppløsningsvæske til parenteral bruk"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "oppl væske til parenteral bruk"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a solvent containing no active substances, intended for use in the preparation of a product for parenteral use."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1208"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073881"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
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"display": "administrable"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002008",
"display": "Solvent"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002043",
"display": "Infusion"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
}
]
},
{
"code": "100000073883",
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"language": "en",
"use": {
"code": "term-name"
},
"value": "Implantation tablet"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Tablett til implantasjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "tab til impl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation prepared by compression of a solid active substance as such or of a formulation thereof into an implant of a size and shape suitable for implantation, usually subcutaneously. Each implantation tablet is presented in a sterile container. Implantation tablets are intended for release over an extended period of time in order to obtain local or systemic effect."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1590"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073883"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
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}
},
{
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002102",
"display": "Tablet"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002036",
"display": "Implantation"
}
}
]
},
{
"code": "100000073885",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Solution for haemofiltration"
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{
"language": "no",
"use": {
"code": "term-name"
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"value": "Hemofiltreringsvæske"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "hemofilt væske"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of an aqueous solution containing electrolytes with a concentration close to the electrolytic composition of plasma, intended for parenteral use in haemofiltration. Glucose may be included."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "288"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073885"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002058",
"display": "Extracorporeal"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002035",
"display": "Dialysis"
}
}
]
},
{
"code": "100000073886",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Solution for haemodialysis"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Hemodialysevæske"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "hemodial væske"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of an aqueous solution containing electrolytes with a concentration close to the electrolytic composition of plasma, intended for use in haemodialysis. Glucose may be included."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "285"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073886"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002058",
"display": "Extracorporeal"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002035",
"display": "Dialysis"
}
}
]
},
{
"code": "100000073888",
"display": "Powder for bladder irrigation",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for bladder irrigation"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til blæreskyllevæske"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til blæreskyll"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in sterile water to obtain a bladder irrigation."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1339"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073888"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002061",
"display": "Intravesical"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002049",
"display": "Rinsing/washing"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073879",
"display": "Bladder irrigation"
}
}
]
},
{
"code": "100000073889",
"display": "Urethral stick",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Urethral stick"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Urethralstift"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "urethralstift"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile single-dose preparation, usually rod-shaped and of a size adapted to the dimensions of the urethra, intended for insertion into the urethra. They may be prepared by compression or moulding."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1648"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073889"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002100",
"display": "Stick"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000032312",
"display": "Urethral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002046",
"display": "Insertion"
}
}
]
},
{
"code": "100000073890",
"display": "Endotracheopulmonary instillation, powder for solution",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Endotracheopulmonary instillation, powder for solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til endotrakeopulmonal instillasjonsvæske, oppløsning"
},
{
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"use": {
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{
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{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002058",
"display": "Extracorporeal"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002053",
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}
}
]
},
{
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{
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{
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},
{
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"value": "Solid sterile single-dose preparation, usually rod-shaped or conical, consisting of active substance(s) dissolved or dispersed in a suitable basis that may dissolve or melt at body temperature, intended to be inserted into wounds."
}
],
"property": [
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"code": "1583"
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},
{
"code": "termIdRms",
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"code": "100000073914"
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},
{
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"display": "Godkjent SPOR"
}
},
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},
{
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"code": "200000002075",
"display": "No transformation",
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}
},
{
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},
{
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{
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},
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},
{
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}
},
{
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},
{
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{
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{
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{
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{
"language": "en",
"use": {
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},
"value": "A radionuclide produced for the radio-labelling of another substance prior to administration."
}
],
"property": [
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},
{
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},
{
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},
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},
{
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"code": "200000002076",
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},
{
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{
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}
},
{
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}
},
{
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"display": "Unknown/Miscellaneous"
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},
{
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}
}
]
},
{
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{
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},
{
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"use": {
"code": "term-description"
},
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}
],
"property": [
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"valueCoding": {
"code": "1392"
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},
{
"code": "termIdRms",
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}
},
{
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},
{
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"display": "Current"
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},
{
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"code": "200000002076",
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}
},
{
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},
{
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},
{
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},
{
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}
},
{
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}
},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002053",
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}
}
]
},
{
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],
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},
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},
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},
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},
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},
{
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},
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},
{
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}
},
{
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}
},
{
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}
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},
{
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],
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},
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},
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},
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},
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"code": "200000002075",
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}
},
{
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}
},
{
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},
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"code": "200000002009",
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}
},
{
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"code": "200000002080",
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}
},
{
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},
{
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"code": "200000002038",
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}
]
},
{
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"use": {
"code": "term-name"
},
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"use": {
"code": "term-name"
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"value": "Oppløsning til organoppbevaring"
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{
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"value": "oppl til organoppbevaring"
},
{
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"use": {
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"value": "Liquid sterile preparation consisting of an aqueous solution of electrolytes typically at a concentration close to the intracellular electrolyte composition, intended for storage, protection and/or perfusion of mammalian body organs that are in particular destined for transplantation."
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],
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},
{
"code": "termIdRms",
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},
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},
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},
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"code": "200000002075",
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},
{
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},
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},
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"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"code": "200000002080",
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}
},
{
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002053",
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]
},
{
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{
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"use": {
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{
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"value": "mageskyllevæske"
},
{
"language": "en",
"use": {
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"value": "Liquid sterile preparation consisting of an aqueous solution intended for irrigation of the stomach."
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],
"property": [
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"code": "998"
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},
{
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},
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},
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},
{
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},
{
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},
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"code": "200000002007",
"display": "Solution"
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},
{
"code": "releaseCharacteristics",
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"code": "200000002080",
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}
},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002029",
"display": "Gastric"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002049",
"display": "Rinsing/washing"
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]
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{
"code": "100000073921",
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"language": "en",
"use": {
"code": "term-name"
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"value": "Kit for radiopharmaceutical preparation"
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{
"language": "no",
"use": {
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"value": "Preparasjonssett til radioaktive legemidler"
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{
"language": "no",
"use": {
"code": "short-name"
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"value": "prep sett til radioaktive legemidler"
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{
"language": "en",
"use": {
"code": "term-description"
},
"value": "A preparation to be reconstituted or combined with radionuclides in the final radiopharmaceutical, usually prior to its administration. The word radiopharmaceutical may be omitted if there is no ambiguity on the radiopharmaceutical nature of the product. Combinations with other standard terms are not recommended."
}
],
"property": [
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"code": "internalCode",
"valueCoding": {
"code": "1268"
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},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073921"
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},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
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},
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"display": "Current"
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},
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"code": "200000002076",
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}
},
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}
},
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},
{
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"code": "200000002016",
"display": "Radiopharmaceutical"
}
},
{
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"code": "200000002080",
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}
},
{
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"code": "200000002070",
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}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
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}
]
},
{
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{
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},
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},
{
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"use": {
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},
"value": "Gastroenteralvæske, emulsjon"
},
{
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"use": {
"code": "short-name"
},
"value": "gastroent væske, emul"
},
{
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"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of an emulsion intended for administration to the stomach or duodenum by means of a suitable applicator."
}
],
"property": [
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"valueCoding": {
"code": "252"
}
},
{
"code": "termIdRms",
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},
{
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},
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"display": "Current"
}
},
{
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}
},
{
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}
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},
{
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"code": "200000002004",
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}
},
{
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"code": "200000002080",
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{
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"code": "200000002030",
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}
},
{
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},
{
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{
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{
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{
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},
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}
],
"property": [
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"code": "1442"
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},
{
"code": "termIdRms",
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},
{
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"display": "Godkjent SPOR"
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},
{
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"display": "Current"
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},
{
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},
{
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}
},
{
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}
},
{
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"code": "200000002007",
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}
},
{
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},
{
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002049",
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}
]
},
{
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{
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"value": "Vevslim"
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{
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"use": {
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{
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"use": {
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"value": "Liquid, more or less viscous, sterile preparation intended for use as tissue glue."
}
],
"property": [
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"code": "1685"
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},
{
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},
{
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},
{
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"display": "Current"
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},
{
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"code": "200000002075",
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}
},
{
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},
{
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},
{
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"code": "200000002007",
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}
},
{
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"code": "200000002080",
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},
{
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"code": "200000002070",
"display": "Unknown/Miscellaneous"
}
},
{
"code": "administrationMethod",
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"code": "200000002039",
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}
]
},
{
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{
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{
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{
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],
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"code": "316"
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},
{
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},
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},
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},
{
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"code": "200000002075",
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},
{
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}
},
{
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},
{
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"code": "200000002089",
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}
},
{
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"code": "200000002080",
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}
},
{
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"code": "200000002070",
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}
},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002053",
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}
]
},
{
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"use": {
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{
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"use": {
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"value": "medisinert svamp"
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{
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},
"value": "Solid preparation consisting of a sponge impregnated with active substance(s); different routes of administration are possible."
}
],
"property": [
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"valueCoding": {
"code": "1001"
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},
{
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},
{
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},
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},
{
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"code": "200000002075",
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"userSelected": false
}
},
{
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}
},
{
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}
},
{
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"code": "200000002089",
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}
},
{
"code": "releaseCharacteristics",
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"code": "200000002080",
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}
},
{
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"code": "200000002070",
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},
{
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"code": "200000002039",
"display": "Application"
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002046",
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}
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},
{
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"code": "term-name"
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"value": "Medicated thread"
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{
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"use": {
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"value": "Medisinert tråd"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "medisinert tråd"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of a biodegradable or non-degradable thread impregnated with active substance(s)."
}
],
"property": [
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"code": "internalCode",
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"code": "42"
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},
{
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},
{
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},
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},
{
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"code": "200000002075",
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}
},
{
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}
},
{
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},
{
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"code": "200000002089",
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}
},
{
"code": "releaseCharacteristics",
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"code": "200000002080",
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}
},
{
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"code": "200000002070",
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002053",
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}
]
},
{
"code": "100000073929",
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"language": "en",
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},
"value": "Medicinal gas, compressed"
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"use": {
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"value": "Medisinsk gass, komprimert"
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{
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"use": {
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"value": "medisinsk gass, komprimert"
},
{
"language": "en",
"use": {
"code": "term-description"
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"value": "A gas packaged under pressure which is entirely gaseous at - 50 °C."
}
],
"property": [
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"valueCoding": {
"code": "1012"
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},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073929"
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},
{
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},
{
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"display": "Current"
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},
{
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"code": "200000002075",
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},
{
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},
{
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002011",
"display": "Medicinal gas"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002067",
"display": "Pulmonary"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002044",
"display": "Inhalation"
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}
]
},
{
"code": "100000073930",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Medicinal gas, liquefied"
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{
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"use": {
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"value": "Medisinsk gass, flytende"
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{
"language": "no",
"use": {
"code": "short-name"
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"value": "medisinsk gass, flytende"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "A gas packaged under pressure, which is partially liquid (gas over liquid) at -50 °C."
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],
"property": [
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"code": "internalCode",
"valueCoding": {
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{
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{
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{
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{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
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{
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{
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},
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"code": "200000002002",
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}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"code": "200000002064",
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}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002068",
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073646",
"display": "Oral solution"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073829",
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}
]
},
{
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{
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"use": {
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"value": "Hudspray, salve"
},
{
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},
"value": "hudspray, salve"
},
{
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},
"value": "Ointment formed at the time of administration from a liquid preparation in a pressurised container with a spray valve or in a container equipped with a spray pump."
}
],
"property": [
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"code": "internalCode",
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},
{
"code": "termIdRms",
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"code": "100000073980"
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},
{
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}
},
{
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},
{
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"code": "200000002075",
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},
{
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{
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},
{
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"code": "200000002107",
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},
{
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},
{
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"code": "200000002055",
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002050",
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]
},
{
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{
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{
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"value": "kons til mikst"
},
{
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},
"value": "Liquid preparation intended to be diluted in the specified liquid to obtain an oral solution."
}
],
"property": [
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"code": "957"
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},
{
"code": "termIdRms",
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},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
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}
},
{
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002071",
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}
},
{
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},
{
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"code": "200000002002",
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},
{
"code": "releaseCharacteristics",
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"code": "200000002080",
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},
{
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"code": "200000002064",
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
}
},
{
"code": "administrableDoseForm",
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}
]
},
{
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{
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{
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{
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"value": "Semi-solid single-dose or multidose preparation consisting of solid particles finely dispersed in a suitable basis, intended for administration on or inside the tooth or on and/or around the nerves supplying the teeth. Toothpaste is excluded."
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],
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},
{
"code": "termIdRms",
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},
{
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},
{
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},
{
"code": "transformation",
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"code": "200000002075",
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},
{
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},
{
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002037",
"display": "Paste"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002056",
"display": "Dental"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
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{
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"use": {
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},
"value": "Ear/eye ointment"
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{
"language": "no",
"use": {
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},
"value": "Øre-/øyesalve"
},
{
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"use": {
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"value": "øre/øyesalve"
},
{
"language": "en",
"use": {
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},
"value": "Semi-solid preparation consisting of an ointment intended for auricular or ocular use."
}
],
"property": [
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"code": "2156"
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},
{
"code": "termIdRms",
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},
{
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}
},
{
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},
{
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"code": "200000002075",
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}
},
{
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}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002107",
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}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
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},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002054",
"display": "Auricular"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002063",
"display": "Ocular"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073779",
"display": "Ear ointment"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073772",
"display": "Eye ointment"
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}
]
},
{
"code": "100000073996",
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{
"language": "en",
"use": {
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"value": "Emulsion for injection/infusion"
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{
"language": "no",
"use": {
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"value": "Injeksjons-/infusjonsvæske, emulsjon"
},
{
"language": "no",
"use": {
"code": "short-name"
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"value": "inj/inf, emul"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile single-dose or multidose preparation consisting of an emulsion intended for administration by injection or infusion."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "803"
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},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000073996"
}
},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
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"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
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}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002004",
"display": "Emulsion"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002043",
"display": "Infusion"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073856",
"display": "Emulsion for injection"
}
},
{
"code": "administrableDoseForm",
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"code": "100000073858",
"display": "Emulsion for infusion"
}
}
]
},
{
"code": "100000074001",
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"language": "en",
"use": {
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},
"value": "Ear/eye drops, solution"
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{
"language": "no",
"use": {
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"value": "Øre-/øyedråper, oppløsning"
},
{
"language": "no",
"use": {
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"value": "øre/øyedr, oppl"
},
{
"language": "en",
"use": {
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},
"value": "Liquid sterile preparation consisting of a solution intended for use as ear drops or eye drops."
}
],
"property": [
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"code": "internalCode",
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"code": "1721"
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},
{
"code": "termIdRms",
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"code": "100000074001"
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},
{
"code": "internalTermStatus",
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},
{
"code": "sourceTermStatus",
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"display": "Current"
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},
{
"code": "transformation",
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"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002054",
"display": "Auricular"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002063",
"display": "Ocular"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002047",
"display": "Instillation"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073786",
"display": "Ear drops, solution"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073759",
"display": "Eye drops, solution"
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}
]
},
{
"code": "100000074003",
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{
"language": "en",
"use": {
"code": "term-name"
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"value": "Endosinusial wash, suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Bihuleskyllevæske, suspensjon"
},
{
"language": "no",
"use": {
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},
"value": "bihuleskyll, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of a suspension intended for cleaning the sinuses."
}
],
"property": [
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"code": "internalCode",
"valueCoding": {
"code": "2157"
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},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074003"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002009",
"display": "Suspension"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002062",
"display": "Nasal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002049",
"display": "Rinsing/washing"
}
}
]
},
{
"code": "100000074004",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Gargle/mouthwash"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Gurglevann/munnskyllevæske"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "gurglevann/munnskyllevæske"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of a solution intended for use as a gargle or a mouthwash."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2158"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074004"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
"display": "Oromucosal"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002042",
"display": "Gargling"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002049",
"display": "Rinsing/washing"
}
}
]
},
{
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{
"language": "en",
"use": {
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},
"value": "Gastro-resistant granules for oral suspension"
},
{
"language": "no",
"use": {
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},
"value": "Enterogranulat til mikstur, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "enterogran til mikst"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of gastro-resistant granules intended to be dispersed in the specified liquid to obtain a gastro-resistant oral suspension."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1794"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074005"
}
},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "NON_CURRENT",
"display": "Non-current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
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}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002086",
"display": "Granules"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002077",
"display": "Delayed"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "200000012529",
"display": "Gastro-resistant oral suspension"
}
}
]
},
{
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Granules for vaginal solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Granulat til vaginalvæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "gran til vag væske, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of aggregated particles that may include excipients to facilitate wetting and dissolution, intended to be dissolved in the specified liquid to obtain a vaginal solution, which is usually prepared just before administration to the patient."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2159"
}
},
{
"code": "termIdRms",
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"code": "100000074007"
}
},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
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}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002086",
"display": "Granules"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002069",
"display": "Vaginal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073813",
"display": "Vaginal solution"
}
}
]
},
{
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{
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"use": {
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},
"value": "Inhalation vapour, effervescent tablet"
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{
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"use": {
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"value": "Brusetablett til inhalasjonsdamp"
},
{
"language": "no",
"use": {
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"value": "brusetab til inh damp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of a tablet usually containing acid substances and carbonates or hydrogen carbonates that react rapidly in the presence of aqueous liquid to release carbon dioxide, intended for generation of vapour to be inhaled to obtain a local effect. The vapour may be generated by adding the tablet to hot water."
}
],
"property": [
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"code": "2160"
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},
{
"code": "termIdRms",
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}
},
{
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},
{
"code": "sourceTermStatus",
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"display": "Current"
}
},
{
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"code": "200000002072",
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}
},
{
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"code": "200000002073",
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}
},
{
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}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002102",
"display": "Tablet"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002067",
"display": "Pulmonary"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002044",
"display": "Inhalation"
}
},
{
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"code": "2289",
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}
]
},
{
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"language": "en",
"use": {
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},
"value": "Inhalation vapour, impregnated pad"
},
{
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"use": {
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},
"value": "Impregnert pute til inhalasjonsdamp"
},
{
"language": "no",
"use": {
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},
"value": "impregnert pute til inh damp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of a piece of absorbent material impregnated usually with a liquid or semi-solid preparation, intended for generation of vapour to be inhaled to obtain a local effect."
}
],
"property": [
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"code": "internalCode",
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"code": "2161"
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},
{
"code": "termIdRms",
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"code": "100000074009"
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},
{
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"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"display": "Current"
}
},
{
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"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002089",
"display": "Impregnated material"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002067",
"display": "Pulmonary"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002044",
"display": "Inhalation"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/fca77bf0-11be-4c33-970e-735453b9da1c",
"code": "2289",
"display": "Inhalation vapour"
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}
]
},
{
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"language": "en",
"use": {
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},
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},
{
"language": "no",
"use": {
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"value": "Mikstur, oppløsning/konsentrat til inhalasjonsvæske til nebulisator, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "mikst oppl/kons til inh væske til nebulisator, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of a solution intended for oral use or intended to be diluted in the specified liquid to obtain a nebuliser solution."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2162"
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},
{
"code": "termIdRms",
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"code": "100000074012"
}
},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002071",
"display": "Dilution",
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}
},
{
"code": "transformation",
"valueCoding": {
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"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002067",
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}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002044",
"display": "Inhalation"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073646",
"display": "Oral solution"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073835",
"display": "Nebuliser solution"
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}
]
},
{
"code": "100000074020",
"display": "Powder for intravesical suspension",
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"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for intravesical suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til intravesikalsuspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til intravesikalsusp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of one or more powders, including freeze-dried powders, intended to be dispersed in the specified liquid to obtain an intravesical suspension."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1372"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074020"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002061",
"display": "Intravesical"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000174025",
"display": "Intravesical suspension"
}
}
]
},
{
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Inhalation powder, tablet"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Inhalasjonspulver, tablett"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "inh pulv, tab"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid multidose preparation intended for inhalation use. The dose of inhalation powder is generated from the tablet by a metering mechanism within the inhaler, for example by scraping off a small amount of powder from the tablet."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2163"
}
},
{
"code": "termIdRms",
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"code": "100000074021"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002102",
"display": "Tablet"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002067",
"display": "Pulmonary"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002044",
"display": "Inhalation"
}
}
]
},
{
"code": "100000074022",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Inhalation vapour, emulsion"
},
{
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"use": {
"code": "term-name"
},
"value": "Emulsjon til inhalasjonsdamp"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "emulsjon til inh damp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of an emulsion intended for generation of vapour to be inhaled to obtain a local effect. The vapour may be generated by adding the emulsion to hot water."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2164"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074022"
}
},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002004",
"display": "Emulsion"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002067",
"display": "Pulmonary"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002044",
"display": "Inhalation"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/fca77bf0-11be-4c33-970e-735453b9da1c",
"code": "2289",
"display": "Inhalation vapour"
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}
]
},
{
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"value": "Modified-release granules for oral suspension"
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{
"language": "no",
"use": {
"code": "term-name"
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"value": "Granulat med modifisert frisetting til mikstur, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
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"value": "gran modif frisetting til mikst, suspensjon"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of modified-release granules intended to be dispersed in the specified liquid to obtain a modified-release oral suspension. The generic term 'Modified-release granules for oral suspension' is used only when the more-specific terms 'Gastro-resistant granules for oral suspension' or 'Prolonged-release granules for oral suspension' do not apply."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2165"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074024"
}
},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "NON_CURRENT",
"display": "Non-current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002086",
"display": "Granules"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002079",
"display": "Modified"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "200000012531",
"display": "Modified-release oral suspension"
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}
]
},
{
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{
"language": "en",
"use": {
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},
"value": "Oral/rectal suspension"
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{
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"use": {
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"value": "Mikstur/rektalvæske, suspensjon"
},
{
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"value": "mikst/rektalvæske susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of a suspension intended for oral or rectal use."
}
],
"property": [
{
"code": "internalCode",
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"code": "1816"
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},
{
"code": "termIdRms",
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"code": "100000074025"
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},
{
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"code": "Godkjent SPOR",
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},
{
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"display": "Current"
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},
{
"code": "transformation",
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"code": "200000002075",
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"userSelected": false
}
},
{
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"display": "manufactured"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002009",
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}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002068",
"display": "Rectal"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
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},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073362",
"display": "Oral suspension"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073830",
"display": "Rectal suspension"
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}
]
},
{
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{
"language": "en",
"use": {
"code": "term-name"
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"value": "Oromucosal patch"
},
{
"language": "no",
"use": {
"code": "term-name"
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"value": "Munnplaster"
},
{
"language": "no",
"use": {
"code": "short-name"
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"value": "munnplaster"
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{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Flexible single-dose preparation intended to be applied to the oral cavity to obtain either a systemic or a local effect by delivering the active substance(s) over a certain period of time, after which it is then removed."
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],
"property": [
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"code": "internalCode",
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"code": "2166"
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},
{
"code": "termIdRms",
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"code": "100000074026"
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},
{
"code": "internalTermStatus",
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"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"display": "Current"
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},
{
"code": "transformation",
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"code": "200000002075",
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}
},
{
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},
{
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},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002094",
"display": "Patch"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
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},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
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}
]
},
{
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"language": "en",
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{
"language": "no",
"use": {
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"value": "Munnvann, oppløsning/laryngofaryngeal oppløsning"
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{
"language": "no",
"use": {
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"value": "munnvann,oppl/laryngofaryngeal oppl"
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{
"language": "en",
"use": {
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"value": "Liquid preparation consisting of a solution intended for oromucosal or laryngopharyngeal use. 'Oromucosal/laryngopharyngeal solution/spray, solution' is excluded."
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],
"property": [
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"code": "internalCode",
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"code": "2167"
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},
{
"code": "termIdRms",
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"code": "100000074027"
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},
{
"code": "internalTermStatus",
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},
{
"code": "sourceTermStatus",
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},
{
"code": "transformation",
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"code": "200000002075",
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}
},
{
"code": "manufacturedAndOrAdministrable",
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},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
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},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
"display": "Oromucosal"
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
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},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073691",
"display": "Oromucosal solution"
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},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000174011",
"display": "Laryngopharyngeal solution"
}
}
]
},
{
"code": "100000074029",
"display": "Powder for concentrate for solution for infusion",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for concentrate for solution for infusion"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til konsentrat til infusjonsvæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til kons til infusjonsvæske, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified liquid to obtain a concentrate for solution for infusion, which must subsequently be diluted before administration as a solution for infusion."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1357"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074029"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002071",
"display": "Dilution",
"userSelected": false
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002043",
"display": "Infusion"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073870",
"display": "Solution for infusion"
}
}
]
},
{
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"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for intravesical solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til intravesikaloppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til intravesikaloppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified liquid to obtain an intravesical solution."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2168"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074033"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002061",
"display": "Intravesical"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000116138",
"display": "Intravesical solution"
}
}
]
},
{
"code": "100000074034",
"display": "Powder for oral/rectal suspension",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for oral/rectal suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til mikstur/rektalvæske, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til mikst/rektalvæske, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of one or more powders, including freeze-dried powders, intended to be dispersed in the specified liquid to obtain an oral/rectal suspension."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1360"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074034"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002068",
"display": "Rectal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073362",
"display": "Oral suspension"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073830",
"display": "Rectal suspension"
}
}
]
},
{
"code": "100000074036",
"display": "Prolonged-release granules for oral suspension",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Prolonged-release granules for oral suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Depotgranulat til mikstur, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "depotgranulat til mikst, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of prolonged-release granules intended to be dispersed in the specified liquid to obtain a prolonged-release oral suspension."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2049"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074036"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "NON_CURRENT",
"display": "Non-current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002086",
"display": "Granules"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "200000012530",
"display": "Prolonged-release oral suspension"
}
}
]
},
{
"code": "100000074037",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Solution for haemodialysis/haemofiltration"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Hemodialyse-/hemofiltreringsvæske"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "hemodial/hemofilt væske"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a solution intended for use as a solution for haemodialysis or a solution for haemofiltration."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1810"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074037"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002058",
"display": "Extracorporeal"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002035",
"display": "Dialysis"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073886",
"display": "Solution for haemodialysis"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073885",
"display": "Solution for haemofiltration"
}
}
]
},
{
"code": "100000074038",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Solution for injection/infusion"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Injeksjons-/infusjonsvæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "inj/inf, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile single-dose or multidose preparation consisting of a solution intended for administration by injection or infusion."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "804"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074038"
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},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
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},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002043",
"display": "Infusion"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073863",
"display": "Solution for injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073870",
"display": "Solution for infusion"
}
}
]
},
{
"code": "100000074044",
"display": "Radiopharmaceutical precursor, solution",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Radiopharmaceutical precursor, solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Stamoppløsning til radioaktive legemidler, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "stamoppl til radioaktivt legemiddel, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of a solution containing a radionuclide produced for the radio-labelling of another substance prior to administration."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1995"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074044"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002016",
"display": "Radiopharmaceutical"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002070",
"display": "Unknown/Miscellaneous"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002053",
"display": "Not specified"
}
}
]
},
{
"code": "100000074054",
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{
"language": "en",
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},
"value": "Powder for solution for intraocular irrigation"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til intraokulær skyllevæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til intraokulær skyllevæske, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified liquid to obtain a solution for intraocular irrigation."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2169"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074054"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002063",
"display": "Ocular"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002049",
"display": "Rinsing/washing"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000174055",
"display": "Solution for intraocular irrigation"
}
}
]
},
{
"code": "100000074055",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Solvent for solution for infusion"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Oppløsningsvæske til infusjonsvæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "oppl væske til inf, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a solvent containing no active substances, intended for use in the preparation of a solution for infusion."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2170"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074055"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002008",
"display": "Solvent"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002043",
"display": "Infusion"
}
}
]
},
{
"code": "100000074058",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Oral drops, powder for suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til dråper, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til dråper, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of one or more powders, including freeze-dried powders, intended to be dispersed in the specified liquid to obtain an oral drops suspension."
}
],
"property": [
{
"code": "internalCode",
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"code": "2171"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074058"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002047",
"display": "Instillation"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073643",
"display": "Oral drops, suspension"
}
}
]
},
{
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Solvent for solution for intraocular irrigation"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Oppløsningsvæske til intraokulær skyllevæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "oppl til intraokulær skyllevæske, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a solvent containing no active substances, intended for use in the preparation of a solution for intraocular irrigation."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2172"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074067"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002008",
"display": "Solvent"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002063",
"display": "Ocular"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002049",
"display": "Rinsing/washing"
}
}
]
},
{
"code": "100000074068",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Dispersion for injection"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Injeksjonsvæske, dispersjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "inj, disp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of two or more phases of which at least one is dispersed in the liquid phase, intended for administration by injection. To be used only when emulsion for injection is not appropriate. Solid suspension preparations are excluded."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "114"
}
},
{
"code": "termIdRms",
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"code": "100000074068"
}
},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002003",
"display": "Dispersion"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
}
]
},
{
"code": "100000074069",
"display": "Concentrate for solution for injection/infusion",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Concentrate for solution for injection/infusion"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Konsentrat til injeksjons-/infusjonsvæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "kons til inj/inf oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation intended to be diluted in the specified liquid to obtain a solution for injection/infusion."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1842"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074069"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002071",
"display": "Dilution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002002",
"display": "Concentrate"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002043",
"display": "Infusion"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073863",
"display": "Solution for injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073870",
"display": "Solution for infusion"
}
}
]
},
{
"code": "100000074070",
"display": "Inhalation solution",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Inhalation solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Inhalasjonsvæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "inh væske, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid, usually multidose preparation consisting of a solution intended for inhalation use. The preparation is presented in a non-pressurised container fitted with a metering dose mechanism. 'Nebuliser solution' and 'Pressurised inhalation, solution' are excluded."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1790"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000074070"
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},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002067",
"display": "Pulmonary"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002044",
"display": "Inhalation"
}
}
]
},
{
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{
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"use": {
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},
"value": "Orodispersible film"
},
{
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"use": {
"code": "term-name"
},
"value": "Munnsmeltende film"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "munnsmeltende film"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of a single- or multilayer sheet of suitable material(s) intended to be placed in the mouth where it disperses rapidly before being swallowed."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1834"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000075573"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
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}
},
{
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002085",
"display": "Film"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002048",
"display": "Orodispersion"
}
}
]
},
{
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"display": "Buccal film",
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"use": {
"code": "term-name"
},
"value": "Buccal film"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Bukkalfilm"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "bukkalfilm"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of a single- or multilayer sheet of suitable material(s) intended to be applied to the buccal cavity (pouch) to obtain a systemic effect."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1866"
}
},
{
"code": "termIdRms",
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"code": "100000075574"
}
},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002085",
"display": "Film"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000032310",
"display": "Buccal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
"code": "100000075576",
"display": "Implantation suspension",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Implantation suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Suspensjon til implantasjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "susp til impl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a suspension intended for implantation in the body; the active substance(s) are released over an extended period of time to obtain a local or systemic effect."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1818"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000075576"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002009",
"display": "Suspension"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002036",
"display": "Implantation"
}
}
]
},
{
"code": "100000075578",
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{
"language": "en",
"use": {
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},
"value": "Concentrate for emulsion for infusion"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Konsentrat til infusjonsvæske, emulsjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "kons til inf emul"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation intended to be diluted in the specified liquid to obtain an emulsion for infusion."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2024"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000075578"
}
},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002071",
"display": "Dilution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002002",
"display": "Concentrate"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002043",
"display": "Infusion"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073858",
"display": "Emulsion for infusion"
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}
]
},
{
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{
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},
{
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"code": "short-name"
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"value": "hudspray, emul"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation, usually multidose, consisting of an emulsion in a pressurised container with a spray valve or in a container equipped with a spray pump, intended for cutaneous use."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2042"
}
},
{
"code": "termIdRms",
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"code": "100000075579"
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},
{
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}
},
{
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"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002075",
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"userSelected": false
}
},
{
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}
},
{
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}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002004",
"display": "Emulsion"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002050",
"display": "Spraying"
}
}
]
},
{
"code": "100000075586",
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"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for implantation suspension"
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"language": "no",
"use": {
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"value": "Pulver til suspensjon til implantasjon"
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{
"language": "no",
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"value": "pulv til susp til implantasjon"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dispersed in the specified liquid to obtain an implantation suspension."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1371"
}
},
{
"code": "termIdRms",
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"code": "100000075586"
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},
{
"code": "internalTermStatus",
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},
{
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"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002072",
"display": "Dispersion",
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}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
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}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002036",
"display": "Implantation"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000075576",
"display": "Implantation suspension"
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}
]
},
{
"code": "100000075589",
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"language": "en",
"use": {
"code": "term-name"
},
"value": "Solution for sealant"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Oppløsning til vevslim"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "oppl til vevslim"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a solution intended for the preparation of a sealant."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1195"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000075589"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002070",
"display": "Unknown/Miscellaneous"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073925",
"display": "Sealant"
}
}
]
},
{
"code": "100000111533",
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{
"language": "en",
"use": {
"code": "term-name"
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"value": "Dispersion for infusion"
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{
"language": "no",
"use": {
"code": "term-name"
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"value": "Infusjonsvæske, dispersjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "inf, disp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of two or more phases of which at least one is dispersed in the liquid phase, intended to be introduced, usually in large volumes, usually into the circulating blood stream. To be used only when emulsion for infusion is not appropriate. Solid suspension preparations are excluded."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1839"
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},
{
"code": "termIdRms",
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},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
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}
},
{
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}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002003",
"display": "Dispersion"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002043",
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}
]
},
{
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},
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},
{
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},
{
"language": "no",
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"code": "short-name"
},
"value": "kons til inf disp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation intended to be diluted in the specified liquid to obtain a dispersion for infusion."
}
],
"property": [
{
"code": "internalCode",
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"code": "2072"
}
},
{
"code": "termIdRms",
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"code": "100000111534"
}
},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002071",
"display": "Dilution",
"userSelected": false
}
},
{
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}
},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002002",
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}
},
{
"code": "releaseCharacteristics",
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"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"code": "200000002066",
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}
},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002043",
"display": "Infusion"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000111533",
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}
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},
{
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{
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"use": {
"code": "term-name"
},
"value": "Munnsalve"
},
{
"language": "no",
"use": {
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},
"value": "munnsalve"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Semi-solid multidose preparation consisting of an ointment intended for oromucosal use. It is applied to the oral cavity or onto a specific part of the oral cavity, to obtain a local effect"
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1828"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000116131"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
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}
},
{
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},
{
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002107",
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}
},
{
"code": "releaseCharacteristics",
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"code": "200000002080",
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},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
"display": "Oromucosal"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
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}
]
},
{
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{
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{
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{
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"use": {
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},
"value": "Semi-solid single-dose or multidose preparation consisting of a single-phase basis of liquids gelled by a suitable gelling agent. Active substance(s) is (are) dissolved or dispersed in the basis, which may be hydrophilic or hydrophobic. Transdermal gels are intended for transdermal use."
}
],
"property": [
{
"code": "internalCode",
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"code": "1978"
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},
{
"code": "termIdRms",
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"code": "100000116134"
}
},
{
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"display": "Godkjent SPOR"
}
},
{
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
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}
},
{
"code": "manufacturedAndOrAdministrable",
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}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002106",
"display": "Gel"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000032309",
"display": "Transdermal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
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{
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},
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{
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},
{
"language": "no",
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"value": "transdermalspray, oppl"
},
{
"language": "en",
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},
"value": "Liquid, usually multidose preparation consisting of a solution in a pressurised container with a spray valve or a container equipped with a spray pump, intended for transdermal use."
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],
"property": [
{
"code": "internalCode",
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"code": "1966"
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},
{
"code": "termIdRms",
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},
{
"code": "internalTermStatus",
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"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000032309",
"display": "Transdermal"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002050",
"display": "Spraying"
}
}
]
},
{
"code": "100000116138",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Intravesical solution"
},
{
"language": "no",
"use": {
"code": "term-name"
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"value": "Intravesikaloppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "intravesikaloppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of an aqueous solution intended for intravesical use by means of a suitable applicator. 'Bladder irrigation' is excluded."
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],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1185"
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},
{
"code": "termIdRms",
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"code": "100000116138"
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},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
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}
},
{
"code": "sourceTermStatus",
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"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
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"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002061",
"display": "Intravesical"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
}
]
},
{
"code": "100000116142",
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{
"language": "en",
"use": {
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},
"value": "Intraperitoneal solution"
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{
"language": "no",
"use": {
"code": "term-name"
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"value": "Intraperitonealoppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "intraperitonealoppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a solution intended for intraperitoneal use. 'Solution for peritoneal dialysis' is excluded."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2174"
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},
{
"code": "termIdRms",
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"code": "100000116142"
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},
{
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},
{
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},
{
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"code": "200000002075",
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}
},
{
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}
},
{
"code": "manufacturedAndOrAdministrable",
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}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002032",
"display": "Intraperitoneal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
}
]
},
{
"code": "100000116145",
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"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Concentrate for intravesical solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Konsentrat til intravesikaloppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "kons til intravesikaloppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation intended to be diluted in the specified liquid to obtain an intravesical solution."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2175"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000116145"
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},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002071",
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"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002002",
"display": "Concentrate"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002061",
"display": "Intravesical"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000116138",
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}
]
},
{
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{
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{
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},
{
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},
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}
],
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},
{
"code": "termIdRms",
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},
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},
{
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},
{
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"code": "200000002002",
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},
{
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{
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"code": "200000002032",
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}
},
{
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},
{
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{
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{
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{
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{
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}
],
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},
{
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},
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},
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},
{
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"code": "200000002075",
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}
},
{
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},
{
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"code": "200000002107",
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}
},
{
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},
{
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"code": "200000002055",
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}
},
{
"code": "intendedSite",
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"code": "200000002062",
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}
},
{
"code": "administrationMethod",
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"code": "200000002039",
"display": "Application"
}
},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073806",
"display": "Nasal ointment"
}
},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073713",
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}
}
]
},
{
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},
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},
{
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"use": {
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},
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},
{
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"use": {
"code": "short-name"
},
"value": "øre/øye/nesedråper, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a solution intended for use as ear drops, eye drops or nasal drops."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2011"
}
},
{
"code": "termIdRms",
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"code": "100000116151"
}
},
{
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},
{
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}
},
{
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"code": "200000002075",
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}
},
{
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}
},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002054",
"display": "Auricular"
}
},
{
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"code": "200000002062",
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},
{
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"code": "200000002063",
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}
},
{
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"code": "200000002047",
"display": "Instillation"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073786",
"display": "Ear drops, solution"
}
},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073759",
"display": "Eye drops, solution"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073794",
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}
]
},
{
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},
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{
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"use": {
"code": "term-name"
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},
{
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"use": {
"code": "short-name"
},
"value": "gran til mikst/rektalvæske, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of granules intended to be dispersed in the specified liquid to obtain an oral/rectal suspension."
}
],
"property": [
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"code": "2208"
}
},
{
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},
{
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},
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},
{
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},
{
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{
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},
{
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},
{
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},
{
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},
{
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},
{
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"code": "200000002052",
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{
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},
{
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"code": "100000073830",
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}
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},
{
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{
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"use": {
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{
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],
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"code": "2249"
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},
{
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},
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},
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},
{
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},
{
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},
{
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"code": "200000002049",
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},
{
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},
{
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{
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{
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"value": "Liquid preparation consisting of a solution intended for nasal or oromucosal application. 'Nasal/oromucosal spray, solution' and 'Nasal spray, solution/oromucosal solution' are excluded."
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],
"property": [
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},
{
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},
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},
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},
{
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"code": "200000002075",
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},
{
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},
{
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"code": "200000002007",
"display": "Solution"
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},
{
"code": "releaseCharacteristics",
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"code": "200000002080",
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},
{
"code": "intendedSite",
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"code": "200000002062",
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},
{
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"code": "200000002065",
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},
{
"code": "administrationMethod",
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"code": "200000002039",
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},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073794",
"display": "Nasal drops, solution"
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},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073691",
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},
{
"code": "100000116164",
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"language": "en",
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"value": "Nasal/oromucosal spray, solution"
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"use": {
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"value": "Nese-/munnspray, oppløsning"
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{
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"value": "nese-/munnspray,oppl"
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{
"language": "en",
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"value": "Liquid preparation consisting of a solution in a container with or without a metering dose valve or in a container with a spray pump, intended for nasal or oromucosal use."
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],
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},
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{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
"display": "Oromucosal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002050",
"display": "Spraying"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073691",
"display": "Oromucosal solution"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000174011",
"display": "Laryngopharyngeal solution"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000173957",
"display": "Laryngopharyngeal spray, solution"
}
}
]
},
{
"code": "100000116180",
"display": "Powder for concentrate for dispersion for infusion",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for concentrate for dispersion for infusion"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til konsentrat til infusjonsvæske, dispersjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til kons til inf væske, disp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dispersed in the specified liquid to obtain a concentrate for dispersion for infusion, which must subsequently be diluted before administration as a dispersion for infusion."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1965"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000116180"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002071",
"display": "Dilution",
"userSelected": false
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002043",
"display": "Infusion"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000111533",
"display": "Dispersion for infusion"
}
}
]
},
{
"code": "100000116181",
"display": "Powder for concentrate for intravesical suspension",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for concentrate for intravesical suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til konsentrat til intravesikalsuspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til kons til intravesikalsusp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dispersed in the specified liquid to obtain a concentrate for intravesical suspension, which must subsequently be diluted before administration as an intravesical suspension."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2245"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000116181"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002071",
"display": "Dilution",
"userSelected": false
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002061",
"display": "Intravesical"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000174025",
"display": "Intravesical suspension"
}
}
]
},
{
"code": "100000116182",
"display": "Powder for concentrate for solution for haemodialysis",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for concentrate for solution for haemodialysis"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til hemodialysekonsentrat"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til hemodial kons"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified liquid to obtain a concentrate for solution for haemodialysis, which must subsequently be diluted before use as a solution for haemodialysis."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2237"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000116182"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002071",
"display": "Dilution",
"userSelected": false
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002058",
"display": "Extracorporeal"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002035",
"display": "Dialysis"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073878",
"display": "Concentrate for solution for haemodialysis"
}
}
]
},
{
"code": "100000116183",
"display": "Powder for concentrate for solution for injection/infusion",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for concentrate for solution for injection/infusion"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til konsentrat til injeksjons-/infusjonsvæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulver til konsentrat til injeksjons-/infusjonsvæske, oppløsning"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified liquid to obtain a concentrate for solution for injection/infusion, which must subsequently be diluted before administration as a solution for injection/infusion."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1359"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000116183"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002071",
"display": "Dilution",
"userSelected": false
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002043",
"display": "Infusion"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073863",
"display": "Solution for injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073870",
"display": "Solution for infusion"
}
}
]
},
{
"code": "100000116184",
"display": "Powder for dental solution",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for dental solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til dentalvæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til dentalvæske, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified liquid to obtain a dental solution."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2242"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000116184"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002056",
"display": "Dental"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073723",
"display": "Dental solution"
}
}
]
},
{
"code": "100000116185",
"display": "Powder for epilesional solution",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for epilesional solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til oppløsning til skadet område"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til oppl til skadet område"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified liquid to obtain an epilesional solution."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2191"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000116185"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002070",
"display": "Unknown/Miscellaneous"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
},
{
"code": "administrableDoseForm",
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"value": "Prolonged-release suspension for injection"
},
{
"language": "no",
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},
"value": "Depotinjeksjonsvæske, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "depotinj væske, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a suspension intended for administration by injection; the active substance(s) are released over an extended period of time."
}
],
"property": [
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"code": "1887"
}
},
{
"code": "termIdRms",
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},
{
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},
{
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"display": "Current"
}
},
{
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"code": "200000002075",
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}
},
{
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},
{
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},
{
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"code": "200000002009",
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}
},
{
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"code": "200000002078",
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},
{
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"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
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}
}
]
},
{
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{
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},
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},
{
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"value": "Liniment, oppløsning/konsentrat til munnvann, oppløsning"
},
{
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{
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},
"value": "Liquid preparation consisting of a solution intended for cutaneous use or intended to be diluted in the specified liquid to obtain an oromucosal solution."
}
],
"property": [
{
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"code": "2220"
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},
{
"code": "termIdRms",
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}
},
{
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},
{
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},
{
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"code": "200000002071",
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}
},
{
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"code": "200000002075",
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}
},
{
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},
{
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},
{
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"code": "200000002080",
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}
},
{
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"code": "200000002055",
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}
},
{
"code": "intendedSite",
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}
},
{
"code": "administrationMethod",
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"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
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"display": "Cutaneous solution"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073691",
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}
]
},
{
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{
"language": "en",
"use": {
"code": "term-name"
},
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},
{
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"use": {
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},
{
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},
"value": "pulv til intravesikal /inj væske, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified liquid to obtain an intravesical solution/solution for injection."
}
],
"property": [
{
"code": "internalCode",
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"code": "1815"
}
},
{
"code": "termIdRms",
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},
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},
{
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"display": "Current"
}
},
{
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"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
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}
},
{
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}
},
{
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},
{
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},
{
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"code": "200000002038",
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}
},
{
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"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
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"code": "100000116138",
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}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073863",
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}
]
},
{
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{
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{
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{
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}
],
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},
{
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},
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{
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},
{
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}
},
{
"code": "intendedSite",
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},
{
"code": "intendedSite",
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},
{
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},
{
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},
{
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},
{
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"code": "100000073863",
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},
{
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{
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{
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"value": "Liquid preparation intended to be diluted in the specified liquid to obtain an oral suspension."
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],
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"code": "958"
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},
{
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},
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},
{
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},
{
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},
{
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},
{
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},
{
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"code": "200000002052",
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},
{
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}
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},
{
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],
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},
{
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},
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},
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},
{
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},
{
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},
{
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"code": "200000002004",
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},
{
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},
{
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002050",
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},
{
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"language": "en",
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"value": "Sublingual spray, solution"
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{
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"value": "Liquid, usually multidose preparation consisting of a solution intended for sublingual use. Sublingual sprays are usually presented in pressurised containers with a metering valve."
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],
"property": [
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"code": "2038"
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},
{
"code": "termIdRms",
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"code": "100000143499"
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},
{
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},
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},
{
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"code": "200000002075",
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},
{
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},
{
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{
"code": "basicDoseForm",
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"code": "200000002007",
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},
{
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"code": "200000002080",
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
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},
{
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{
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{
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{
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},
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}
],
"property": [
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},
{
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},
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},
{
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},
{
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{
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{
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},
{
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"code": "200000002009",
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},
{
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"code": "200000002080",
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},
{
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},
{
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},
{
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{
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{
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{
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}
],
"property": [
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"code": "2185"
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},
{
"code": "termIdRms",
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},
{
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},
{
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},
{
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"code": "200000002075",
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}
},
{
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},
{
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002027",
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}
},
{
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"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"code": "200000002056",
"display": "Dental"
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
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},
{
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"language": "en",
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{
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"value": "pulv til dentalsement"
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{
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"use": {
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},
"value": "Solid preparation consisting of one or more powders, including freeze-dried powders, intended for use in the preparation of a dental cement."
}
],
"property": [
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"code": "internalCode",
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"code": "2234"
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},
{
"code": "termIdRms",
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},
{
"code": "internalTermStatus",
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},
{
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"display": "Current"
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},
{
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"code": "200000002074",
"display": "Mixing",
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}
},
{
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"display": "manufactured"
}
},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002056",
"display": "Dental"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000143501",
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}
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},
{
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"value": "oppl til dentalsement"
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{
"language": "en",
"use": {
"code": "term-description"
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"value": "Liquid preparation consisting of a solution intended for use in the preparation of a dental cement."
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],
"property": [
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"code": "2226"
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},
{
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},
{
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},
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},
{
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"code": "200000002074",
"display": "Mixing",
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}
},
{
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002056",
"display": "Dental"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000143501",
"display": "Dental cement"
}
}
]
},
{
"code": "100000143523",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for dispersion for infusion"
},
{
"language": "no",
"use": {
"code": "term-name"
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"value": "Pulver til infusjonsvæske, dispersjon"
},
{
"language": "no",
"use": {
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"value": "pulv til inf væske disp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dispersed in the specified liquid to obtain a dispersion for infusion."
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],
"property": [
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"code": "internalCode",
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"code": "2063"
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},
{
"code": "termIdRms",
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"code": "100000143523"
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},
{
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},
{
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"code": "CURRENT",
"display": "Current"
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},
{
"code": "transformation",
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"code": "200000002072",
"display": "Dispersion",
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}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002043",
"display": "Infusion"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000111533",
"display": "Dispersion for infusion"
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}
]
},
{
"code": "100000143524",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Implantation matrix"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Matriks til implantasjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "matriks til implantasjon"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of a usually pliable, absorbent piece of material (e.g. collagen), usually impregnated with a liquid preparation, intended for implantation in the body. The material may be cut into smaller pieces before implantation, and may be shaped around a tissue (e.g. a bone) or inserted into a medical device that is then implanted. Implantation matrices are intended for release over an extended period of time, usually in order to obtain a local effect. Usually the matrix disappears with time. When the product is packaged as a separate matrix, powder and solvent (or matrix and solution), which are used to prepare the implantation matrix immediately before use, the appropriate combined term should be used; see for example ‘Powder, solvent and matrix for implantation matrix’."
}
],
"property": [
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"code": "internalCode",
"valueCoding": {
"code": "1960"
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},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000143524"
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},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
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},
{
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"code": "CURRENT",
"display": "Current"
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},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002088",
"display": "Implant"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002036",
"display": "Implantation"
}
}
]
},
{
"code": "100000143525",
"display": "Powder for cutaneous solution",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for cutaneous solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til liniment, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til liniment, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified liquid to obtain a cutaneous solution."
}
],
"property": [
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"code": "internalCode",
"valueCoding": {
"code": "2244"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000143525"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073731",
"display": "Cutaneous solution"
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}
]
},
{
"code": "100000143526",
"display": "Powder for solution for iontophoresis",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for solution for iontophoresis"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til iontoforeseoppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til iontoforeseoppl"
},
{
"language": "en",
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"code": "term-description"
},
"value": "Solid preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified liquid to obtain a solution for iontophoresis."
}
],
"property": [
{
"code": "internalCode",
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"code": "2196"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000143526"
}
},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
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"code": "MANUFACTURED",
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}
},
{
"code": "basicDoseForm",
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"code": "200000002099",
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}
},
{
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},
{
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"code": "200000032309",
"display": "Transdermal"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073734",
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}
]
},
{
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{
"language": "en",
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},
"value": "Solution for cardioplegia"
},
{
"language": "no",
"use": {
"code": "term-name"
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"value": "Oppløsning til kardioplegi"
},
{
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"use": {
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},
"value": "oppl til kardioplegi"
},
{
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"code": "term-description"
},
"value": "Liquid sterile preparation consisting of an aqueous solution intended for cardioplegic use. Some preparations may require mixing with other preparations prior to administration, for example to adjust the pH."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2084"
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},
{
"code": "termIdRms",
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"code": "100000143527"
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},
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},
{
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},
{
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"code": "200000002075",
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},
{
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},
{
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"code": "200000002007",
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},
{
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},
{
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"code": "200000002066",
"display": "Parenteral"
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
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},
{
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{
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}
],
"property": [
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"code": "2211"
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},
{
"code": "termIdRms",
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},
{
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},
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},
{
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"code": "200000002075",
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},
{
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},
{
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},
{
"code": "basicDoseForm",
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"code": "200000002089",
"display": "Impregnated material"
}
},
{
"code": "releaseCharacteristics",
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"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"code": "200000002070",
"display": "Unknown/Miscellaneous"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002053",
"display": "Not specified"
}
}
]
},
{
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{
"language": "en",
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{
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{
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{
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"value": "Liquid preparation consisting of a solution intended for use as a gargle or a nasal wash."
}
],
"property": [
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"code": "2210"
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},
{
"code": "termIdRms",
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},
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},
{
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"display": "Current"
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},
{
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"code": "200000002075",
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"userSelected": false
}
},
{
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}
},
{
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"code": "200000002007",
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},
{
"code": "releaseCharacteristics",
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"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"code": "200000002062",
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},
{
"code": "intendedSite",
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"code": "200000002065",
"display": "Oromucosal"
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002042",
"display": "Gargling"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002049",
"display": "Rinsing/washing"
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},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073673",
"display": "Gargle"
}
},
{
"code": "administrableDoseForm",
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"code": "100000073810",
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}
]
},
{
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"use": {
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"value": "Impregnert plugg til inhalasjonsdamp"
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{
"language": "no",
"use": {
"code": "short-name"
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"value": "impregnert plugg til inh damp"
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{
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"code": "term-description"
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"value": "Solid preparation consisting of an impregnated plug that generates a vapour to be inhaled, for example by the patient inhaling through a device containing the plug, thereby drawing air through or over it and vaporising the active ingredient(s) impregnated therein."
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],
"property": [
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"code": "internalCode",
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"code": "2212"
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},
{
"code": "termIdRms",
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"code": "100000143551"
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},
{
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},
{
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},
{
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"code": "200000002075",
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},
{
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},
{
"code": "basicDoseForm",
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"code": "200000002089",
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},
{
"code": "releaseCharacteristics",
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"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"code": "200000002067",
"display": "Pulmonary"
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002044",
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},
{
"code": "administrableDoseForm",
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}
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},
{
"code": "100000145128",
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"language": "en",
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{
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"value": "øre/nesedr, susp"
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{
"language": "en",
"use": {
"code": "term-description"
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"value": "Liquid preparation consisting of a suspension intended for use as ear drops or nasal drops."
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],
"property": [
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"code": "internalCode",
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"code": "2186"
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},
{
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},
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},
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},
{
"code": "transformation",
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"code": "200000002075",
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},
{
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},
{
"code": "basicDoseForm",
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"code": "200000002009",
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},
{
"code": "releaseCharacteristics",
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"code": "200000002080",
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},
{
"code": "intendedSite",
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"code": "200000002054",
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},
{
"code": "intendedSite",
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"code": "200000002062",
"display": "Nasal"
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},
{
"code": "administrationMethod",
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"code": "200000002047",
"display": "Instillation"
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},
{
"code": "administrableDoseForm",
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"code": "100000073780",
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},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073807",
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}
]
},
{
"code": "100000156088",
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"language": "en",
"use": {
"code": "term-name"
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"value": "Sealant matrix"
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{
"language": "no",
"use": {
"code": "term-name"
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"value": "Matriks til vevslim"
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{
"language": "no",
"use": {
"code": "short-name"
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"value": "matriks til vevslim"
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{
"language": "en",
"use": {
"code": "term-description"
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"value": "Solid sterile preparation consisting of a pliable piece of material impregnated or coated with a sealant or with a powder that forms a sealant after contact with an appropriate fluid (e.g. blood). It may act as a haemostatic agent and/or tissue glue. The matrix may itself form part of the seal, and is usually absorbed by the body over time."
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],
"property": [
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"code": "internalCode",
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"code": "1959"
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},
{
"code": "termIdRms",
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"code": "100000156088"
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},
{
"code": "internalTermStatus",
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},
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"code": "sourceTermStatus",
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"display": "Current"
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},
{
"code": "transformation",
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"code": "200000002075",
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"userSelected": false
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},
{
"code": "manufacturedAndOrAdministrable",
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"display": "manufactured"
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},
{
"code": "manufacturedAndOrAdministrable",
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},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002089",
"display": "Impregnated material"
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},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"code": "200000002070",
"display": "Unknown/Miscellaneous"
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},
{
"code": "administrationMethod",
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"code": "200000002039",
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]
},
{
"code": "100000157838",
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"language": "en",
"use": {
"code": "term-name"
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"value": "Sealant powder"
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{
"language": "no",
"use": {
"code": "term-name"
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"value": "Vevslimpulver"
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{
"language": "no",
"use": {
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"value": "vevslimpulv"
},
{
"language": "en",
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},
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],
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
"display": "Oromucosal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002050",
"display": "Spraying"
}
}
]
},
{
"code": "100000173958",
"display": "Matrix for implantation matrix",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Matrix for implantation matrix"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Matriks til matriks til implantasjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "matriks til matriks til implantasjon"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of a usually pliable, absorbent piece of material (e.g. collagen) intended to be used in the preparation of an implantation matrix."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2221"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000173958"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002089",
"display": "Impregnated material"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002036",
"display": "Implantation"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000143524",
"display": "Implantation matrix"
}
}
]
},
{
"code": "100000173960",
"display": "Nasal drops, powder for solution",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Nasal drops, powder for solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til nesedråper, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til nesedr, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified liquid to obtain a nasal drops solution."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2250"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000173960"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002062",
"display": "Nasal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002047",
"display": "Instillation"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073794",
"display": "Nasal drops, solution"
}
}
]
},
{
"code": "100000173961",
"display": "Powder for gel",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for gel"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til gel"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "Pulv til gel"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of one or more powders intended to be mixed with the specified liquid or gel to obtain a gel (for cutaneous use)."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "1502"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000173961"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073726",
"display": "Gel"
}
}
]
},
{
"code": "100000173962",
"display": "Powder for dental gel",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for dental gel"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til dentalgel"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til dentalgel"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of one or more powders intended to be mixed with the specified liquid or gel to obtain a dental gel."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2233"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000173962"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002056",
"display": "Dental"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073705",
"display": "Dental gel"
}
}
]
},
{
"code": "100000173963",
"display": "Powder for dispersion for injection",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for dispersion for injection"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til injeksjonsvæske, dispersjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til inj væske, dispersjon"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dispersed in the specified liquid to obtain a dispersion for injection."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2238"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000173963"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000074068",
"display": "Dispersion for injection"
}
}
]
},
{
"code": "100000173964",
"display": "Powder for endocervical gel",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for endocervical gel"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til endocervikalgel"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til endocervikalgel"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of one or more powders intended to be mixed with the specified liquid or gel to obtain an endocervical gel."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2235"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000173964"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002028",
"display": "Endocervical"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073903",
"display": "Endocervical gel"
}
}
]
},
{
"code": "100000173965",
"display": "Powder for endosinusial solution",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for endosinusial solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til bihulevæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til bihulevæske, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified liquid to obtain an endosinusial solution."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2240"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000173965"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002062",
"display": "Nasal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000174021",
"display": "Endosinusial solution"
}
}
]
},
{
"code": "100000173966",
"display": "Powder for intraocular instillation solution",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for intraocular instillation solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til intraokulær instillasjonsvæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
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{
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],
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},
{
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},
{
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},
{
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},
{
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},
{
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},
{
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},
{
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},
{
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},
{
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},
{
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],
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},
{
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{
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},
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},
{
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},
{
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},
{
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{
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},
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}
],
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},
{
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},
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},
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},
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},
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},
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},
{
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},
{
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"code": "200000002044",
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},
{
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],
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},
{
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},
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},
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},
{
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}
},
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},
{
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},
{
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}
},
{
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},
{
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"code": "200000002039",
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},
{
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{
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{
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],
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},
{
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},
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},
{
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},
{
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},
{
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},
{
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}
},
{
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
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},
{
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"code": "100000073864",
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},
{
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{
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{
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],
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},
{
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},
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},
{
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},
{
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"code": "200000002074",
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}
},
{
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},
{
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"code": "200000002003",
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},
{
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"code": "200000002080",
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},
{
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},
{
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"code": "200000002043",
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000111533",
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}
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{
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{
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"value": "pulv til øredråper, susp"
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{
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"value": "Solid preparation consisting of one or more powders, including freeze-dried powders, intended to be dispersed in the specified liquid to obtain an ear drops suspension."
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],
"property": [
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"code": "2251"
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},
{
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"code": "100000174001"
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},
{
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},
{
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},
{
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"code": "200000002072",
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},
{
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},
{
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"code": "200000002099",
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},
{
"code": "releaseCharacteristics",
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"code": "200000002080",
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},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002054",
"display": "Auricular"
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002047",
"display": "Instillation"
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},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073780",
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}
]
},
{
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"language": "en",
"use": {
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"value": "Effervescent granules for oral suspension"
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"use": {
"code": "term-name"
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{
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"value": "brusegranulat til mikst, susp"
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{
"language": "en",
"use": {
"code": "term-description"
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"value": "Solid preparation consisting of effervescent granules intended to be dispersed or dissolved in the specified liquid, which is supplied in the same packaging, to obtain an oral suspension. Where the granules are intended to be dispersed in water, the term 'Effervescent granules' is used instead."
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],
"property": [
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"code": "internalCode",
"valueCoding": {
"code": "2199"
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},
{
"code": "termIdRms",
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"code": "100000174002"
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},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
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},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002086",
"display": "Granules"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073362",
"display": "Oral suspension"
}
}
]
},
{
"code": "100000174003",
"display": "Emulsion for emulsion for injection",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Emulsion for emulsion for injection"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Emulsjon til injeksjonsvæske, emulsjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "emul til inj, emul"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of an emulsion intended for use in the preparation of an emulsion for injection."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2202"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174003"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002004",
"display": "Emulsion"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073856",
"display": "Emulsion for injection"
}
}
]
},
{
"code": "100000174004",
"display": "Endotracheopulmonary instillation, powder for suspension",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Endotracheopulmonary instillation, powder for suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til endotrakeopulmonal instillasjonsvæske, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til endotrakeopulm inst væske susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of one or more powders, including freeze-dried powders, intended to be dispersed in the specified liquid to obtain an endotracheopulmonary instillation suspension."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2045"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174004"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002067",
"display": "Pulmonary"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002047",
"display": "Instillation"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073902",
"display": "Endotracheopulmonary instillation, suspension"
}
}
]
},
{
"code": "100000174005",
"display": "Eye drops, powder for solution",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Eye drops, powder for solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til øyedråper, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til øyedr, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified liquid to obtain an eye drops solution."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2259"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174005"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002063",
"display": "Ocular"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002047",
"display": "Instillation"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073759",
"display": "Eye drops, solution"
}
}
]
},
{
"code": "100000174006",
"display": "Eye drops, powder for suspension",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Eye drops, powder for suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til øyedråper, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til øyedr, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of one or more powders, including freeze-dried powders, intended to be dispersed in the specified liquid to obtain an eye drops suspension."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2253"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174006"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002063",
"display": "Ocular"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002047",
"display": "Instillation"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073760",
"display": "Eye drops, suspension"
}
}
]
},
{
"code": "100000174007",
"display": "Gas for dispersion for infusion",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Gas for dispersion for infusion"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Gass til infusjonsvæske, dispersjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "gass til inf væske, disp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Sterile preparation consisting of a gas that is intended to be mixed with the specified liquid to obtain a dispersion of the gas in the liquid, which is intended for administration by infusion."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2203"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174007"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002011",
"display": "Medicinal gas"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002043",
"display": "Infusion"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000111533",
"display": "Dispersion for infusion"
}
}
]
},
{
"code": "100000174008",
"display": "Gas for dispersion for injection",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Gas for dispersion for injection"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Gass til injeksjonsvæske, dispersjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "gass til inj, disp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Sterile preparation consisting of a gas that is intended to be mixed with the specified liquid to obtain a dispersion of the gas in the liquid, which is intended for administration by injection."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2205"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174008"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002011",
"display": "Medicinal gas"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000074068",
"display": "Dispersion for injection"
}
}
]
},
{
"code": "100000174009",
"display": "Gel for gel",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Gel for gel"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Gel til gel"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "gel til gel"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Semi-solid preparation consisting of a gel intended for use in the preparation of a gel for cutaneous use."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2206"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174009"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002106",
"display": "Gel"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073726",
"display": "Gel"
}
}
]
},
{
"code": "100000174010",
"display": "Granules for rectal suspension",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Granules for rectal suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Granulat til rektalvæske, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "gran til rektalvæske,susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of aggregated particles that may include excipients to facilitate wetting and dispersion, intended to be dispersed in the specified liquid to obtain a rectal suspension, which is usually prepared just before administration to the patient."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2209"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174010"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002086",
"display": "Granules"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002068",
"display": "Rectal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073830",
"display": "Rectal suspension"
}
}
]
},
{
"code": "100000174011",
"display": "Laryngopharyngeal solution",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Laryngopharyngeal solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Laryngofaryngeal oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "laryngofaryngeal oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of a solution intended for administration to the laryngopharynx for a local effect, other than by spraying."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2219"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174011"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
"display": "Oromucosal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
}
]
},
{
"code": "100000174012",
"display": "Powder for gingival gel",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for gingival gel"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til gel til tannkjøtt"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til gel til tannkjøtt"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of one or more powders intended to be mixed with the specified liquid or gel to obtain a gingival gel."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2236"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174012"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
"display": "Oromucosal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073680",
"display": "Gingival gel"
}
}
]
},
{
"code": "100000174013",
"display": "Powder for implantation matrix",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for implantation matrix"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til matriks til implantasjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulver til matriks til implantasjon"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be used in the preparation of an implantation matrix, e.g. by dissolving in the specified liquid to prepare the solution used to impregnate the matrix."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2247"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174013"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002036",
"display": "Implantation"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000143524",
"display": "Implantation matrix"
}
}
]
},
{
"code": "100000174014",
"display": "Powder for implantation paste",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for implantation paste"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til pasta til implantasjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til pasta til implantasjon"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders intended to be mixed with the specified liquid or paste to obtain an implantation paste."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2248"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174014"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002036",
"display": "Implantation"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000174023",
"display": "Implantation paste"
}
}
]
},
{
"code": "100000174015",
"display": "Solvent for...",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Solvent for..."
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Oppløsningsvæske til…"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "oppl væske til..."
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of an excipient that contains no active substances itself but is intended to be used in the preparation of a pharmaceutical product, e.g. for diluting/dissolving/dispersing the item(s) containing the active substance(s). The term is intended to cover all such excipients, with the particular specifications (e.g. sterility requirements) depending on the final product and its intended use."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2197"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174015"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002008",
"display": "Solvent"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002070",
"display": "Unknown/Miscellaneous"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002053",
"display": "Not specified"
}
}
]
},
{
"code": "100000174016",
"display": "Suspension for emulsion for injection",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Suspension for emulsion for injection"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Suspensjon til injeksjonsvæske, emulsjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "susp til inj væske, emul"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a suspension intended for use in the preparation of an emulsion for injection."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2256"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174016"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002009",
"display": "Suspension"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073856",
"display": "Emulsion for injection"
}
}
]
},
{
"code": "100000174017",
"display": "Suspension for oral suspension",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Suspension for oral suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Suspensjon til mikstur, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "susp til mikst, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of a suspension intended for use in the preparation of an oral suspension."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2073"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174017"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002009",
"display": "Suspension"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073362",
"display": "Oral suspension"
}
}
]
},
{
"code": "100000174019",
"display": "Suspension for suspension for injection",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Suspension for suspension for injection"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Suspensjon til injeksjonsvæske, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "susp til inj væske, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a suspension intended for use in the preparation of a suspension for injection."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2257"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174019"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002009",
"display": "Suspension"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073864",
"display": "Suspension for injection"
}
}
]
},
{
"code": "100000174020",
"display": "Powder for emulsion for injection",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for emulsion for injection"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til injeksjonsvæske, emulsjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til inj væske, emulsjon"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be mixed with the specified liquid to obtain an emulsion for injection."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2239"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174020"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073856",
"display": "Emulsion for injection"
}
}
]
},
{
"code": "100000174021",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Endosinusial solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Bihulevæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "bihulevæske, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of a solution intended to be administered to the sinuses to obtain a local effect."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2198"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174021"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002062",
"display": "Nasal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
}
]
},
{
"code": "100000174022",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Epilesional solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Oppløsning til skadet område"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "oppl til skadet område"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a solution intended to be administered onto a lesion."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2230"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174022"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002070",
"display": "Unknown/Miscellaneous"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
}
]
},
{
"code": "100000174023",
"display": "Implantation paste",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Implantation paste"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pasta til implantasjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pasta til implantasjon"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Semi-solid sterile preparation containing large proportions of solids finely dispersed in the basis, intended to be implanted in the body for release of the active substance(s) over an extended period of time, usually to obtain a systemic effect."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2231"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174023"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002037",
"display": "Paste"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002036",
"display": "Implantation"
}
}
]
},
{
"code": "100000174024",
"display": "Intraocular instillation solution",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Intraocular instillation solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Intraokulær instillasjonsvæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "intraokulær inst væske, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a solution intended to be instilled as drops into an internal part of the eye."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2192"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174024"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002063",
"display": "Ocular"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002047",
"display": "Instillation"
}
}
]
},
{
"code": "100000174025",
"display": "Intravesical suspension",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Intravesical suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Intravesikalsuspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "intravesikalsusp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of a small-volume suspension intended for intravesical use by means of a suitable applicator."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2194"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174025"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002009",
"display": "Suspension"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002061",
"display": "Intravesical"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
}
]
},
{
"code": "100000174026",
"display": "Gas for dispersion for injection/infusion",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Gas for dispersion for injection/infusion"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Gass til injeksjons-/infusjonsvæske, dispersjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "gass til inj-/inf væske, dispersjon"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Sterile preparation consisting of a gas that is intended to be mixed with the specified liquid to obtain a dispersion of the gas in the liquid, which is intended for administration by injection or infusion."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2204"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174026"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002011",
"display": "Medicinal gas"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002043",
"display": "Infusion"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000074068",
"display": "Dispersion for injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000111533",
"display": "Dispersion for infusion"
}
}
]
},
{
"code": "100000174027",
"display": "Powder for sealant",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for sealant"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til vevslim"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til vevslim"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified liquid to obtain a sealant."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2187"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174027"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002070",
"display": "Unknown/Miscellaneous"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073925",
"display": "Sealant"
}
}
]
},
{
"code": "100000174028",
"display": "Powder for solution for skin-prick test",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for solution for skin-prick test"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til prikktest, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til prikktest, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified liquid to obtain a solution for skin-prick test."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2258"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174028"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073756",
"display": "Solution for skin-prick test"
}
}
]
},
{
"code": "100000174029",
"display": "Solution for solution for injection",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Solution for solution for injection"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Oppløsning til injeksjonsvæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "oppl til inj væske, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a solution intended for use in the preparation of a solution for injection."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2228"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174029"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073863",
"display": "Solution for injection"
}
}
]
},
{
"code": "100000174031",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Coated granules"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Granulat, drasjert"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "granulat, drasjert"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation intended for oral use, consisting of granules coated with one or more layers of mixtures of various substances that are usually applied as a solution or suspension in conditions in which evaporation of the vehicle occurs. The thickness of the coating is greater than that of film-coated granules. When the coating dissolves or disintegrates any active substance is released into the gastrointestinal fluid at a rate depending essentially on its intrinsic properties (conventional release)."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2112"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174031"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002086",
"display": "Granules"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073372",
"display": "Granules"
}
}
]
},
{
"code": "100000174032",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Solution for suspension for injection"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Oppløsning til injeksjonsvæske, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "oppl til inj væske, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a solution intended for use in the preparation of a suspension for injection."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2229"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174032"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073864",
"display": "Suspension for injection"
}
}
]
},
{
"code": "100000174033",
"display": "Granules for suspension for injection",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Granules for suspension for injection"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Granulat til injeksjonsvæske, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "granulat til inj, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of granules intended to be dispersed in the specified liquid to obtain a suspension for injection."
}
],
"property": [
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"code": "internalCode",
"valueCoding": {
"code": "2207"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "100000174033"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002086",
"display": "Granules"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073864",
"display": "Suspension for injection"
}
}
]
},
{
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{
"language": "en",
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},
"value": "Dispersion for injection/infusion"
},
{
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},
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},
{
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},
"value": "inj/inf, disp"
},
{
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},
"value": "Sterile liquid preparation consisting of two or more phases of which at least one is dispersed in the liquid phase, intended for administration by injection or infusion. To be used only when emulsion for injection/infusion is not appropriate. Solid suspension preparations are excluded."
}
],
"property": [
{
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"valueCoding": {
"code": "2213"
}
},
{
"code": "termIdRms",
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"code": "100000174034"
}
},
{
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
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"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
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}
},
{
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"code": "200000002003",
"display": "Dispersion"
}
},
{
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"code": "200000002080",
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}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
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}
},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002043",
"display": "Infusion"
}
},
{
"code": "administrationMethod",
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},
{
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"code": "100000074068",
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}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000111533",
"display": "Dispersion for infusion"
}
}
]
},
{
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"display": "Solution for injection/skin-prick test",
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"use": {
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},
"value": "Solution for injection/skin-prick test"
},
{
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"use": {
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},
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},
{
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},
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},
{
"language": "en",
"use": {
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},
"value": "Liquid sterile preparation consisting of a solution containing an allergen product intended for diagnostic use in a skin-prick test or as an injection (usually intraepidermal); it may also be licensed for immunotherapy treatment by injection (usually subcutaneous)."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2053"
}
},
{
"code": "termIdRms",
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},
{
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"code": "Godkjent SPOR",
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},
{
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"display": "Current"
}
},
{
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"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073863",
"display": "Solution for injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073756",
"display": "Solution for skin-prick test"
}
}
]
},
{
"code": "100000174048",
"display": "Powder for solution for injection/skin-prick test",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for solution for injection/skin-prick test"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til injeksjonsvæske/prikktest, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til inj væske/prikktest, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified liquid to obtain a solution for injection/skin-prick test."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2246"
}
},
{
"code": "termIdRms",
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"code": "100000174048"
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},
{
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},
{
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"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002073",
"display": "Dissolution",
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}
},
{
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"display": "manufactured"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073863",
"display": "Solution for injection"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073756",
"display": "Solution for skin-prick test"
}
}
]
},
{
"code": "100000174051",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Solution for solution for infusion"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Oppløsning til infusjonsvæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "oppl til inf væske, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a solution intended for use in the preparation of a solution for infusion."
}
],
"property": [
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"code": "2227"
}
},
{
"code": "termIdRms",
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"code": "100000174051"
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},
{
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},
{
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},
{
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"code": "200000002074",
"display": "Mixing",
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}
},
{
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"display": "manufactured"
}
},
{
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"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002043",
"display": "Infusion"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073870",
"display": "Solution for infusion"
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}
]
},
{
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},
"value": "Tablet for cutaneous solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Tablett til liniment, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "tab til liniment, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid, usually single-dose preparation consisting of a tablet, usually uncoated, intended to be dissolved in the specified liquid to obtain a cutaneous solution."
}
],
"property": [
{
"code": "internalCode",
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"code": "2260"
}
},
{
"code": "termIdRms",
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"code": "100000174052"
}
},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
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}
},
{
"code": "sourceTermStatus",
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"display": "Current"
}
},
{
"code": "transformation",
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"code": "200000002073",
"display": "Dissolution",
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}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002102",
"display": "Tablet"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
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}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrableDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073731",
"display": "Cutaneous solution"
}
}
]
},
{
"code": "100000174055",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Solution for intraocular irrigation"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Intraokulær skyllevæske, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "intraokulær skyllevæske, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a solution intended for irrigation of one or more internal structures of the eye, for example during surgical procedures."
}
],
"property": [
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"code": "internalCode",
"valueCoding": {
"code": "2193"
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},
{
"code": "termIdRms",
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"code": "100000174055"
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},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
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},
{
"code": "sourceTermStatus",
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"display": "Current"
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},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
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}
},
{
"code": "manufacturedAndOrAdministrable",
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"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002063",
"display": "Ocular"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002049",
"display": "Rinsing/washing"
}
}
]
},
{
"code": "200000002229",
"display": "Granules in capsule for opening",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Granules in capsule for opening"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Granulat i kapsel som åpnes"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "gran i kaps som åpnes"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Single-dose preparation consisting of granules enclosed in a capsule resembling a hard capsule. The capsule is to be opened and its entire contents administered orally. The capsule itself is not swallowed and is discarded after opening. For preparations consisting of a capsule that may either be swallowed whole or be opened, the term 'Hard capsule' is used instead."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2065"
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},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000002229"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
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{
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],
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{
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{
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},
{
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{
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],
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},
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{
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},
{
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},
{
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{
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],
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},
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{
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{
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],
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"code": "200000002073",
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}
},
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},
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},
{
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{
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{
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"value": "intrauteringel"
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{
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"value": "Semi-solid preparation consisting of a gel intended for intrauterine use."
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],
"property": [
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},
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},
{
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"code": "200000002075",
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{
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},
{
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002106",
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},
{
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{
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{
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{
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"use": {
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{
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"value": "inh væske, disp"
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"value": "Liquid preparation consisting of a dispersion intended for inhalation use. The dispersion is converted into an aerosol by a continuously operating nebuliser or a metered-dose nebuliser."
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],
"property": [
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},
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"code": "200000002003",
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"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002067",
"display": "Pulmonary"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002044",
"display": "Inhalation"
}
}
]
},
{
"code": "200000004719",
"display": "Tablet with sensor",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Tablet with sensor"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Tablett med sensor"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "tab med sensor"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid single-dose preparation consisting of a tablet intended for oral use, in which one or more ingestible sensors are embedded. The sensor is usually not digested, and is usually intended for use with external diagnostic equipment to which it can transmit data such as physiological and behavioural measurements."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2100"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000004719"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002102",
"display": "Tablet"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
}
}
]
},
{
"code": "200000005069",
"display": "Medicinal leech",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Medicinal leech"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Medisinsk blodigle"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "blodigle"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Whole, live, medicinal leech, usually of the Hirudo genus (e.g. Hirudo medicinalis, Hirudo verbana), usually intended to be applied to the skin in order to restore or improve local blood flow or to provide other local effects. After attaching itself to the host, the leech creates an incision in the skin and secretes saliva containing a variety of active substances (e.g. anaesthetics, anticoagulants, anti-inflammatories, vasodilators) that allow it to feed on the blood of the host."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2015"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000005069"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000005071",
"display": "Live animal"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
"code": "200000005113",
"display": "Medicinal larvae",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Medicinal larvae"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Medisinsk larve"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "larve"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Whole, live, medicinal larvae, usually of a species of fly such as Lucilla sericata (common greenbottle fly), provided in an appropriate container such as a mesh bag, intended to be applied to a wound and covered with an appropriate dressing in order to allow debridement of necrotic tissue over a specified period of time (usually a few days). The larvae secrete enzymes into the wound, liquefying the necrotic tissue, and ingest the resulting material."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2309"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000005113"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000005071",
"display": "Live animal"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
"code": "200000010390",
"display": "Urethral ointment",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Urethral ointment"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Urethralsalve"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "urethralsalve"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Semi-solid preparation consisting of an ointment intended for urethral use by means of a suitable applicator."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2286"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000010390"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002107",
"display": "Ointment"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000032312",
"display": "Urethral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
}
]
},
{
"code": "200000010456",
"display": "Prolonged-release wound solution",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Prolonged-release wound solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Depotsåroppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "depotsåroppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a solution intended to be administered onto a wound, including surgical wounds; the active substance(s) are released over an extended period of time."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2269"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000010456"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002070",
"display": "Unknown/Miscellaneous"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
}
]
},
{
"code": "200000010610",
"display": "Prolonged-release dispersion for injection",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Prolonged-release dispersion for injection"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Depotinjeksjonsvæske, dispersjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "depotinj væske, disp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of two or more phases of which at least one is dispersed in the liquid phase, intended for administration by injection; the active substance(s) are released over an extended period of time. To be used only when 'Prolonged-release emulsion for injection' is not appropriate. Solid suspension preparations are excluded."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2271"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000010610"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002003",
"display": "Dispersion"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
}
]
},
{
"code": "200000010684",
"display": "Sublingual lyophilisate",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Sublingual lyophilisate"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Sublingvalt lyofilisat"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "Sublingvalt lyofil"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid single-dose preparation made by freeze-drying of a liquid or semi-solid preparation, intended for sublingual use."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2281"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000010684"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002092",
"display": "Lyophilisate"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000032311",
"display": "Sublingual"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
}
]
},
{
"code": "200000012529",
"display": "Gastro-resistant oral suspension",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Gastro-resistant oral suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Enteromikstur, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "enteromikst, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid, single-dose or multidose, delayed-release preparation consisting of a suspension intended for oral use. The preparation is intended to resist the gastric fluid and release the active substance(s) in the intestinal fluid. Each dose from a multidose container is administered by means of a device suitable for measuring the prescribed volume. The device is usually a spoon or a cup for volumes of 5 mL or multiples thereof or an oral syringe for other volumes."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2285"
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},
{
"code": "termIdRms",
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},
{
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
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},
{
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"display": "Current"
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},
{
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"code": "200000002075",
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}
},
{
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{
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{
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"code": "200000002009",
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}
},
{
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"code": "200000002077",
"display": "Delayed"
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},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
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}
]
},
{
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{
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{
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{
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{
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}
],
"property": [
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},
{
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},
{
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"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"display": "Current"
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},
{
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"code": "200000002075",
"display": "No transformation",
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}
},
{
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},
{
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{
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},
{
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}
},
{
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"code": "200000002064",
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
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{
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{
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{
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{
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}
],
"property": [
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},
{
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},
{
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},
{
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"display": "Current"
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},
{
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}
},
{
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}
},
{
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"code": "200000002079",
"display": "Modified"
}
},
{
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"code": "200000002064",
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
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{
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{
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{
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}
],
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},
{
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},
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},
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},
{
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"code": "200000002071",
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}
},
{
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}
},
{
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"code": "200000002002",
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}
},
{
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"code": "200000002080",
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002045",
"display": "Injection"
}
},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000074068",
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}
]
},
{
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{
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},
{
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"use": {
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},
"value": "Non-sterile, liquid preparation consisting of a solution intended for cutaneous or oromucosal use; it is not intended for use on injured skin."
}
],
"property": [
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},
{
"code": "termIdRms",
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},
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},
{
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"display": "Current"
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},
{
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"code": "200000002075",
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}
},
{
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
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},
{
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}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
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},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
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},
{
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"code": "100000073731",
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},
{
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}
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},
{
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{
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{
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"value": "munnhulepose"
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{
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"use": {
"code": "term-description"
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"value": "Solid single-dose preparation consisting of a small bag made of a suitable material containing a preparation such as a powder; it is intended to be placed in the oral cavity to obtain either a systemic or a local effect by delivering the active substance(s) over a certain period of time, after which it is then removed."
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],
"property": [
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"code": "2304"
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},
{
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},
{
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},
{
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},
{
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"code": "200000002075",
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}
},
{
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},
{
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},
{
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"code": "200000002026",
"display": "Pouch"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
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},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
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]
},
{
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{
"language": "en",
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"value": "Impregnated cutaneous swab"
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{
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"use": {
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"value": "Impregnert vattpinne til bruk på hud"
},
{
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"use": {
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"value": "impreg vattpinne til bruk på hud"
},
{
"language": "en",
"use": {
"code": "term-description"
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"value": "Solid preparation consisting of a piece of absorbent material impregnated usually with a liquid preparation, intended to be applied to the skin for a limited period of time with one or more wiping motions, and which may be attached to an application device such as a stick. Impregnated pad is excluded."
}
],
"property": [
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"code": "2277"
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},
{
"code": "termIdRms",
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"code": "200000017728"
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},
{
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"display": "Godkjent SPOR"
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},
{
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"display": "Current"
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},
{
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"code": "200000002075",
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}
},
{
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},
{
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},
{
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002089",
"display": "Impregnated material"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
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}
]
},
{
"code": "200000017730",
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"language": "en",
"use": {
"code": "term-name"
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"value": "Prolonged-release pessary"
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{
"language": "no",
"use": {
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},
"value": "Depotvagitorie"
},
{
"language": "no",
"use": {
"code": "short-name"
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"value": "depotvagitorie"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid, single-dose preparation usually prepared by moulding, of various shapes, usually ovoid, with a volume and consistency suitable for insertion into the vagina to obtain a local effect. It contains one or more active substances dispersed or dissolved in a suitable basis that may be soluble or dispersible in water or may melt at body temperature. It shows a slower release of the active substance(s) than that of a conventional-release pessary. Prolonged release is achieved by a special formulation design and/or manufacturing method."
}
],
"property": [
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"code": "internalCode",
"valueCoding": {
"code": "2311"
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},
{
"code": "termIdRms",
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"code": "200000017730"
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},
{
"code": "internalTermStatus",
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
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},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
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},
{
"code": "transformation",
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{
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{
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},
{
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},
{
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{
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},
{
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},
{
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],
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},
{
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{
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{
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},
{
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{
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],
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},
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},
{
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},
{
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"code": "200000002080",
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{
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"code": "200000002066",
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},
{
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},
{
"code": "administrableDoseForm",
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{
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],
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},
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},
{
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{
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},
{
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{
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],
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},
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},
{
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},
{
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"code": "200000002102",
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},
{
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"code": "200000002078",
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{
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},
{
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"code": "200000002041",
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},
{
"code": "administrationMethod",
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"code": "200000002052",
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{
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{
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"use": {
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{
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{
"language": "en",
"use": {
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"value": "Liquid preparation intended to be diluted in the specified liquid to obtain a cutaneous emulsion."
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],
"property": [
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"code": "2283"
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},
{
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{
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{
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{
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"code": "200000002039",
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},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073719",
"display": "Cutaneous emulsion"
}
}
]
},
{
"code": "200000030000",
"display": "Powder for prolonged-release oral suspension",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for prolonged-release oral suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til depotmikstur, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til depotmikst, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of a powder intended to be dispersed in the specified liquid to obtain a prolonged-release oral suspension."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2341"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000030000"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "200000012530",
"display": "Prolonged-release oral suspension"
}
}
]
},
{
"code": "200000031084",
"display": "Suspension for gel",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Suspension for gel"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Suspensjon til gel"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "susp til gel"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid preparation consisting of a suspension intended to be mixed with the specified liquid or gel to obtain a gel (for cutaneous use)."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2325"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000031084"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002009",
"display": "Suspension"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002055",
"display": "Cutaneous"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002039",
"display": "Application"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073726",
"display": "Gel"
}
}
]
},
{
"code": "200000032295",
"display": "Powder for solution for provocation test",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for solution for provocation test"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til oppløsning til provokasjonstest"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til oppl til provokasjonstest"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of one or more powders, including freeze-dried powders, intended to be dissolved in the specified liquid to obtain a solution for provocation test."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2332"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000032295"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002073",
"display": "Dissolution",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002062",
"display": "Nasal"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002063",
"display": "Ocular"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002067",
"display": "Pulmonary"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002053",
"display": "Not specified"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "100000073944",
"display": "Solution for provocation test"
}
}
]
},
{
"code": "200000032317",
"display": "Oromucosal drops, emulsion",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Oromucosal drops, emulsion"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Munndråper, emulsjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "munndr, emul"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid, usually multidose preparation consisting of an emulsion intended for oromucosal use. The preparation is administered in small volumes into the oral cavity or onto a specific part of the oral cavity by means of a suitable device such as a dropper."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2328"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000032317"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002004",
"display": "Emulsion"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
"display": "Oromucosal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002047",
"display": "Instillation"
}
}
]
},
{
"code": "200000032318",
"display": "Oromucosal drops, solution",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Oromucosal drops, solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Munndråper, oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "munndr, oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid, usually multidose preparation consisting of a solution intended for oromucosal use. The preparation is administered in small volumes into the oral cavity or onto a specific part of the oral cavity by means of a suitable device such as a dropper."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2326"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000032318"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
"display": "Oromucosal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002047",
"display": "Instillation"
}
}
]
},
{
"code": "200000032319",
"display": "Oromucosal drops, suspension",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Oromucosal drops, suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Munndråper, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "munndr, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid, usually multidose preparation consisting of a suspension intended for oromucosal use. The preparation is administered in small volumes into the oral cavity or onto a specific part of the oral cavity by means of a suitable device such as a dropper."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2327"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000032319"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002009",
"display": "Suspension"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002065",
"display": "Oromucosal"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002047",
"display": "Instillation"
}
}
]
},
{
"code": "200000032420",
"display": "Granules for gastro-resistant oral suspension",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Granules for gastro-resistant oral suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Granulat til enteromikstur, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "gran til enteromikst, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of granules intended to be dispersed in the specified liquid to obtain a gastro-resistant oral suspension."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2339"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000032420"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002086",
"display": "Granules"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002077",
"display": "Delayed"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "200000012529",
"display": "Gastro-resistant oral suspension"
}
}
]
},
{
"code": "200000032421",
"display": "Powder for gastro-resistant oral suspension",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Powder for gastro-resistant oral suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver til enteromikstur, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv til enteromikst, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of a powder intended to be dispersed in the specified liquid to obtain a gastro-resistant oral suspension."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2345"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000032421"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002077",
"display": "Delayed"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "200000012529",
"display": "Gastro-resistant oral suspension"
}
}
]
},
{
"code": "200000032422",
"display": "Granules for modified-release oral suspension",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Granules for modified-release oral suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Granulat til mikstur med modifisert frisetting, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "gran til mikst modif frisetting, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of granules intended to be dispersed in the specified liquid to obtain a modified-release oral suspension. The generic term 'Granules for modified-release oral suspension' is used only when the more-specific terms 'Granules for gastro-resistant oral suspension' or 'Granules for prolonged-release oral suspension' do not apply."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2344"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000032422"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002086",
"display": "Granules"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002079",
"display": "Modified"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "200000012531",
"display": "Modified-release oral suspension"
}
}
]
},
{
"code": "200000032423",
"display": "Granules for prolonged-release oral suspension",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Granules for prolonged-release oral suspension"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Granulat til depotmikstur, suspensjon"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "gran til depotmikst, susp"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid preparation consisting of granules intended to be dispersed in the specified liquid to obtain a prolonged-release oral suspension."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2338"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000032423"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002072",
"display": "Dispersion",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002086",
"display": "Granules"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "200000012530",
"display": "Prolonged-release oral suspension"
}
}
]
},
{
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{
"language": "en",
"use": {
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"value": "Implantation gel"
},
{
"language": "no",
"use": {
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},
"value": "Gel til implantasjon"
},
{
"language": "no",
"use": {
"code": "short-name"
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"value": "gel til impl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Semi-solid sterile preparation consisting of a gel intended to be implanted in the body; the active substance(s) are released over an extended period of time to obtain a local or systemic effect."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2340"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000032717"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002106",
"display": "Gel"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002036",
"display": "Implantation"
}
}
]
},
{
"code": "200000032718",
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"language": "en",
"use": {
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},
"value": "Dispersion for implantation gel"
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{
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"use": {
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"value": "Dispersjon til gel til implantasjon"
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{
"language": "no",
"use": {
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"value": "disp til gel til impl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a dispersion intended for the preparation of an implantation gel."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2337"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000032718"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002003",
"display": "Dispersion"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002036",
"display": "Implantation"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "200000032717",
"display": "Implantation gel"
}
}
]
},
{
"code": "200000032719",
"display": "Solution for implantation gel",
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{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Solution for implantation gel"
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{
"language": "no",
"use": {
"code": "term-name"
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"value": "Oppløsning til gel til implantasjon"
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{
"language": "no",
"use": {
"code": "short-name"
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"value": "oppl til gel til impl"
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{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid sterile preparation consisting of a solution intended for the preparation of an implantation gel."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2342"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000032719"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002074",
"display": "Mixing",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "basicDoseForm",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002066",
"display": "Parenteral"
}
},
{
"code": "administrationMethod",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002036",
"display": "Implantation"
}
},
{
"code": "administrableDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/c32a474c-be97-4e15-8977-5d0ae6acfaf8",
"code": "200000032717",
"display": "Implantation gel"
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}
]
},
{
"code": "200000041090",
"display": "Intracameral implant",
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{
"language": "en",
"use": {
"code": "term-name"
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"value": "Intracameral implant"
},
{
"language": "no",
"use": {
"code": "term-name"
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"value": "Intrakameralt implantat"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "Intrakameralt implantat"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation of a size and shape suitable for implantation into the anterior chamber of the eye; the active substance(s) are released over an extended period of time, usually to obtain a local effect. Each intracameral implant is usually presented in a sterile administration device such as an applicator."
}
],
"property": [
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"code": "internalCode",
"valueCoding": {
"code": "2298"
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},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000041090"
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},
{
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"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
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},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
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},
{
"code": "transformation",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002088",
"display": "Implant"
}
},
{
"code": "releaseCharacteristics",
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"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002063",
"display": "Ocular"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002036",
"display": "Implantation"
}
}
]
},
{
"code": "200000041091",
"display": "Intravitreal implant",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Intravitreal implant"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Intravitrealt implantat"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "intravitrealt implantat"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid sterile preparation of a size and shape suitable for implantation into the rear chamber of the eye; the active substance(s) are released over an extended period of time, usually to obtain a local effect. Each intravitreal implant is usually presented in a sterile administration device such as an applicator."
}
],
"property": [
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"code": "internalCode",
"valueCoding": {
"code": "2297"
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},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000041091"
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},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
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},
{
"code": "sourceTermStatus",
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"code": "CURRENT",
"display": "Current"
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},
{
"code": "transformation",
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"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
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"code": "ADMINISTRABLE",
"display": "administrable"
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},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002088",
"display": "Implant"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002063",
"display": "Ocular"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002036",
"display": "Implantation"
}
}
]
},
{
"code": "200000044182",
"display": "Sublingual solution",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Sublingual solution"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Sublingval oppløsning"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "Sublingval oppl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Liquid single-dose or multidose preparation consisting of a solution intended for sublingual use."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2305"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000044182"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002007",
"display": "Solution"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000032311",
"display": "Sublingual"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002038",
"display": "Administration"
}
}
]
},
{
"code": "200000044203",
"display": "Oral powder in capsule for opening",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Oral powder in capsule for opening"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Pulver i kapsel som åpnes"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "pulv i kaps som åpnes"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Single-dose preparation consisting of an oral powder enclosed in a capsule resembling a hard capsule. The capsule is to be opened and its entire contents administered orally. The capsule itself is not swallowed and is discarded after opening. For preparations consisting of a capsule that may either be swallowed whole or be opened, the term 'Hard capsule' is used instead."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2270"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000044203"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002099",
"display": "Powder"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002080",
"display": "Conventional"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002064",
"display": "Oral"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002052",
"display": "Swallowing"
}
}
]
},
{
"code": "200000044330",
"display": "Intravesical delivery system",
"designation": [
{
"language": "en",
"use": {
"code": "term-name"
},
"value": "Intravesical delivery system"
},
{
"language": "no",
"use": {
"code": "term-name"
},
"value": "Intravesikalinnlegg"
},
{
"language": "no",
"use": {
"code": "short-name"
},
"value": "intravesikalinnl"
},
{
"language": "en",
"use": {
"code": "term-description"
},
"value": "Solid single-dose delivery system intended for intravesical use that releases its contents of active substance(s) over an extended period of time."
}
],
"property": [
{
"code": "internalCode",
"valueCoding": {
"code": "2330"
}
},
{
"code": "termIdRms",
"valueCoding": {
"code": "200000044330"
}
},
{
"code": "internalTermStatus",
"valueCoding": {
"code": "Godkjent SPOR",
"display": "Godkjent SPOR"
}
},
{
"code": "sourceTermStatus",
"valueCoding": {
"code": "CURRENT",
"display": "Current"
}
},
{
"code": "transformation",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/d84a6cbc-c61a-4405-9e6f-cdf3d2961f60",
"code": "200000002075",
"display": "No transformation",
"userSelected": false
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "MANUFACTURED",
"display": "manufactured"
}
},
{
"code": "manufacturedAndOrAdministrable",
"valueCoding": {
"code": "ADMINISTRABLE",
"display": "administrable"
}
},
{
"code": "basicDoseForm",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/054ca9cd-2c77-4d0f-bf59-04572fda8ddc",
"code": "200000002019",
"display": "System"
}
},
{
"code": "releaseCharacteristics",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/b423da1b-d2c8-4bfb-a41e-1e01a076ab77",
"code": "200000002078",
"display": "Prolonged"
}
},
{
"code": "intendedSite",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/6420a269-7680-470f-ad5b-3b3836a8a812",
"code": "200000002061",
"display": "Intravesical"
}
},
{
"code": "administrationMethod",
"valueCoding": {
"system": "https://api.legemiddelverket.no/FHIR-R4/CodeSystem/3fcc383e-f893-43b6-8a62-d3f0c81a68df",
"code": "200000002046",
"display": "Insertion"
}
}
]
}
]
}