| Package | eu.epi.february2025 |
| Resource Type | CodeSystem |
| Id | 300000000001 |
| FHIR Version | R5 |
| Source | https://simplifier.net/resolve?scope=eu.epi.february2025@1.0.0&canonical=http://ema.europa.eu/fhir/CodeSystem/300000000001 |
| URL | http://ema.europa.eu/fhir/CodeSystem/300000000001 |
| Version | 5.0.0 |
| Status | active |
| Name | EUepismpccodesystem |
| Title | EU EPI SmPC QRD code values |
| Description | EU EPI SmPC QRD code values |
| Content | complete |
No resources found
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No narrative content found in resource
{
"resourceType": "CodeSystem",
"status": "active",
"content": "complete",
"name": "EUepismpccodesystem",
"id": "300000000001",
"title": "EU EPI SmPC QRD code values",
"description": "EU EPI SmPC QRD code values",
"version": "5.0.0",
"url": "http://ema.europa.eu/fhir/CodeSystem/300000000001",
"concept": [
{
"code": "000000000000",
"display": "Code for custom sub-sections (reserved)"
},
{
"code": "000000000004",
"display": "Code for custom sub-sections (level 4)"
},
{
"code": "000000000005",
"display": "Code for custom sub-sections (level 5)"
},
{
"code": "200000029791",
"display": "SUMMARY OF PRODUCT CHARACTERISTICS"
},
{
"code": "200000029792",
"display": "1. NAME OF THE MEDICINAL PRODUCT"
},
{
"code": "200000029793",
"display": "2. QUALITATIVE AND QUANTITATIVE COMPOSITION"
},
{
"code": "200000029794",
"display": "2.1 General description"
},
{
"code": "200000029795",
"display": "2.2 Qualitative and quantitative composition"
},
{
"code": "200000029796",
"display": "Excipient(s) with known effect"
},
{
"code": "200000029797",
"display": "3. PHARMACEUTICAL FORM"
},
{
"code": "200000029798",
"display": "4. CLINICAL PARTICULARS"
},
{
"code": "200000029799",
"display": "4.1 Therapeutic indications"
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{
"code": "200000029800",
"display": "4.2 Posology and method of administration"
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{
"code": "200000029801",
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{
"code": "200000029802",
"display": "Paediatric population"
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{
"code": "200000029803",
"display": "Method of administration"
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{
"code": "200000029804",
"display": "Precautions to be taken before handling or administering the medicinal product"
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{
"code": "200000029805",
"display": "4.3 Contraindications"
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{
"code": "200000029806",
"display": "4.4 Special warnings and precautions for use"
},
{
"code": "200000029807",
"display": "Traceability"
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{
"code": "200000029808",
"display": "Paediatric population"
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{
"code": "200000029809",
"display": "4.5 Interaction with other medicinal products and other forms of interaction"
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{
"code": "200000029810",
"display": "Paediatric population"
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{
"code": "200000029811",
"display": "4.6 Fertility, pregnancy and lactation"
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{
"code": "200000029812",
"display": "Pregnancy"
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{
"code": "200000029813",
"display": "Breast-feeding"
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{
"code": "200000029814",
"display": "Fertility"
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{
"code": "200000029815",
"display": "4.7 Effects on ability to drive and use machines"
},
{
"code": "200000029816",
"display": "4.8 Undesirable effects"
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{
"code": "200000029817",
"display": "Paediatric population"
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{
"code": "200000029818",
"display": "Reporting of suspected adverse reactions"
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{
"code": "200000029819",
"display": "4.9 Overdose"
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{
"code": "200000029820",
"display": "Paediatric population"
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{
"code": "200000029821",
"display": "5. PHARMACOLOGICAL PROPERTIES"
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{
"code": "200000029822",
"display": "5.1 Pharmacodynamic properties"
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{
"code": "200000029823",
"display": "Mechanism of action"
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{
"code": "200000029824",
"display": "Pharmacodynamic effects"
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{
"code": "200000029825",
"display": "Clinical efficacy and safety"
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{
"code": "200000029826",
"display": "Paediatric population"
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{
"code": "200000029827",
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{
"code": "200000029828",
"display": "Absorption"
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{
"code": "200000029829",
"display": "Distribution"
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{
"code": "200000029830",
"display": "Biotransformation"
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{
"code": "200000029831",
"display": "Elimination"
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{
"code": "200000029832",
"display": "Linearity/non-linearity"
},
{
"code": "200000029833",
"display": "Pharmacokinetic/pharmacodynamic relationship(s)"
},
{
"code": "200000029834",
"display": "5.3 Preclinical safety data"
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{
"code": "200000029835",
"display": "Environmental risk assessment (ERA)"
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{
"code": "200000029836",
"display": "6. PHARMACEUTICAL PARTICULARS"
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{
"code": "200000029837",
"display": "6.1 List of excipients"
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{
"code": "200000029838",
"display": "6.2 Incompatibilities"
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{
"code": "200000029839",
"display": "6.3 Shelf life"
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{
"code": "200000029840",
"display": "6.4 Special precautions for storage"
},
{
"code": "200000029841",
"display": "6.5 Nature and contents of container <and special equipment for use, administration or implantation>"
},
{
"code": "200000029842",
"display": "6.6 Special precautions for disposal <and other handling>"
},
{
"code": "200000029843",
"display": "Use in the paediatric population"
},
{
"code": "200000029844",
"display": "7. MARKETING AUTHORISATION HOLDER"
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{
"code": "200000029845",
"display": "8. MARKETING AUTHORISATION NUMBER(S)"
},
{
"code": "200000029846",
"display": "9. DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION"
},
{
"code": "200000029847",
"display": "10. DATE OF REVISION OF THE TEXT"
},
{
"code": "200000029848",
"display": "11. DOSIMETRY"
},
{
"code": "200000029849",
"display": "12. INSTRUCTIONS FOR PREPARATION OF RADIOPHARMACEUTICALS"
}
],
"experimental": false,
"publisher": "European Medicines Agency",
"jurisdiction": [
{
"text": "European Union"
}
],
"caseSensitive": true,
"count": 62
}