FHIR IG Statistics: StructureDefinition/AdverseEvent
Resources that use this resource
Resources that this resource uses
Narrative
Note: links and images are rebased to the (stated) source
Source
{
"resourceType": "StructureDefinition",
"id": "AdverseEvent",
"text": {
"status": "extensions",
"div": "<!-- snip (see above) -->"
},
"url": "http://hl7.eu/fhir/ig/idea4rc/StructureDefinition/AdverseEvent",
"version": "0.1.0",
"name": "AdverseEventI4RC",
"title": "Adverse Event",
"status": "draft",
"date": "2025-07-21T15:34:12+00:00",
"publisher": "IDEA4RC Project",
"contact": [
{
"name": "IDEA4RC Project",
"telecom": [
{
"system": "url",
"value": "https://www.idea4rc.eu/"
}
]
},
{
"name": "IDEA4RC Project",
"telecom": [
{
"system": "url",
"value": "https://www.idea4rc.eu/"
}
]
}
],
"description": "Adverse Event\nMaturity Level: 0 Draft",
"jurisdiction": [
{
"coding": [
{
"system": "http://unstats.un.org/unsd/methods/m49/m49.htm",
"code": "150",
"display": "Europe"
}
]
}
],
"fhirVersion": "4.0.1",
"kind": "logical",
"abstract": false,
"type": "http://hl7.eu/fhir/ig/idea4rc/StructureDefinition/AdverseEvent",
"baseDefinition": "http://hl7.org/fhir/StructureDefinition/Base",
"derivation": "specialization",
"snapshot": {
"extension": [
{
"url": "http://hl7.org/fhir/tools/StructureDefinition/snapshot-base-version",
"valueString": "4.0.1"
}
],
"element": [
{
"id": "AdverseEvent",
"path": "AdverseEvent",
"short": "Adverse Event",
"definition": "Adverse Event\nMaturity Level: 0 Draft",
"min": 0,
"max": "*",
"base": {
"path": "Base",
"min": 0,
"max": "*"
},
"isModifier": false
},
{
"id": "AdverseEvent.treatmentReference[x]",
"extension": [
{
"extension": [
{
"url": "code",
"valueCode": "SHALL:handle"
},
{
"url": "actor",
"valueCanonical": "http://hl7.eu/fhir/ig/idea4rc/actor-headneck-i4rc"
},
{
"url": "http://hl7.org/fhir/tools/StructureDefinition/snapshot-source",
"valueUri": "http://hl7.eu/fhir/ig/idea4rc/StructureDefinition/AdverseEvent|0.1.0"
}
],
"url": "http://hl7.org/fhir/StructureDefinition/obligation"
}
],
"path": "AdverseEvent.treatmentReference[x]",
"short": "Treatment reference (M)",
"definition": "Treatment element containing the data regarding the specific treatment. It can be SystemicTreatment, Surgery, Radiotherapy, Isolated Limb Perfusion or Regional Deep Hyperthemia \nOBSERVATION or CONDITION",
"min": 1,
"max": "*",
"base": {
"path": "AdverseEvent.treatmentReference[x]",
"min": 1,
"max": "*"
},
"type": [
{
"code": "http://hl7.eu/fhir/ig/idea4rc/StructureDefinition/SystemicTreatment"
},
{
"code": "http://hl7.eu/fhir/ig/idea4rc/StructureDefinition/Radiotherapy"
},
{
"code": "http://hl7.eu/fhir/ig/idea4rc/StructureDefinition/Surgery"
}
]
},
{
"id": "AdverseEvent.adverseEventType",
"extension": [
{
"extension": [
{
"url": "code",
"valueCode": "SHALL:handle"
},
{
"url": "actor",
"valueCanonical": "http://hl7.eu/fhir/ig/idea4rc/actor-headneck-i4rc"
},
{
"url": "http://hl7.org/fhir/tools/StructureDefinition/snapshot-source",
"valueUri": "http://hl7.eu/fhir/ig/idea4rc/StructureDefinition/AdverseEvent|0.1.0"
}
],
"url": "http://hl7.org/fhir/StructureDefinition/obligation"
}
],
"path": "AdverseEvent.adverseEventType",
"short": "Adverse event type (CTCAE Term) (M)",
"definition": "the Common Terminology Criteria for Adverse Events (CTCAE) is used to identify the adverse events. It includes details of the adverse event type and grade \nOBSERVATION or CONDITION (check)",
"min": 1,
"max": "*",
"base": {
"path": "AdverseEvent.adverseEventType",
"min": 1,
"max": "*"
},
"type": [
{
"code": "CodeableConcept"
}
]
},
{
"id": "AdverseEvent.adverseEventStartingDate",
"extension": [
{
"extension": [
{
"url": "code",
"valueCode": "SHALL:handle"
},
{
"url": "actor",
"valueCanonical": "http://hl7.eu/fhir/ig/idea4rc/actor-headneck-i4rc"
},
{
"url": "http://hl7.org/fhir/tools/StructureDefinition/snapshot-source",
"valueUri": "http://hl7.eu/fhir/ig/idea4rc/StructureDefinition/AdverseEvent|0.1.0"
}
],
"url": "http://hl7.org/fhir/StructureDefinition/obligation"
}
],
"path": "AdverseEvent.adverseEventStartingDate",
"short": "Adverse event starting date (M)",
"definition": "specifies when adverse events begins \nOBSERVATION or CONDITION (check)",
"min": 1,
"max": "*",
"base": {
"path": "AdverseEvent.adverseEventStartingDate",
"min": 1,
"max": "*"
},
"type": [
{
"code": "date"
}
]
},
{
"id": "AdverseEvent.adverseEventDuration",
"extension": [
{
"extension": [
{
"url": "code",
"valueCode": "SHALL:handle"
},
{
"url": "actor",
"valueCanonical": "http://hl7.eu/fhir/ig/idea4rc/actor-headneck-i4rc"
},
{
"url": "http://hl7.org/fhir/tools/StructureDefinition/snapshot-source",
"valueUri": "http://hl7.eu/fhir/ig/idea4rc/StructureDefinition/AdverseEvent|0.1.0"
}
],
"url": "http://hl7.org/fhir/StructureDefinition/obligation"
}
],
"path": "AdverseEvent.adverseEventDuration",
"short": "Adverse event duration (M)",
"definition": "specifies the duration of the adverse event \nOBSERVATION or CONDITION (check)\n\nAdverse Events in OMOP ar standard conditions or observations and duration must be derived from that data\n\nhttps://forums.ohdsi.org/t/mapping-adverse-event-data-to-omop-and-to-fhir/15373",
"comment": "Less than one week - 2000100050\nMore than one week but less than a month - 2000100051\nMore than a month but less than 3 months - 2000100052\nMore than 3 months - 2000100053",
"min": 1,
"max": "*",
"base": {
"path": "AdverseEvent.adverseEventDuration",
"min": 1,
"max": "*"
},
"type": [
{
"code": "CodeableConcept"
}
]
}
]
},
"differential": {
"element": [
{
"id": "AdverseEvent",
"path": "AdverseEvent",
"short": "Adverse Event",
"definition": "Adverse Event\nMaturity Level: 0 Draft"
},
{
"id": "AdverseEvent.treatmentReference[x]",
"extension": [
{
"extension": [
{
"url": "code",
"valueCode": "SHALL:handle"
},
{
"url": "actor",
"valueCanonical": "http://hl7.eu/fhir/ig/idea4rc/actor-headneck-i4rc"
}
],
"url": "http://hl7.org/fhir/StructureDefinition/obligation"
}
],
"path": "AdverseEvent.treatmentReference[x]",
"short": "Treatment reference (M)",
"definition": "Treatment element containing the data regarding the specific treatment. It can be SystemicTreatment, Surgery, Radiotherapy, Isolated Limb Perfusion or Regional Deep Hyperthemia \nOBSERVATION or CONDITION",
"min": 1,
"max": "*",
"type": [
{
"code": "http://hl7.eu/fhir/ig/idea4rc/StructureDefinition/SystemicTreatment"
},
{
"code": "http://hl7.eu/fhir/ig/idea4rc/StructureDefinition/Radiotherapy"
},
{
"code": "http://hl7.eu/fhir/ig/idea4rc/StructureDefinition/Surgery"
}
]
},
{
"id": "AdverseEvent.adverseEventType",
"extension": [
{
"extension": [
{
"url": "code",
"valueCode": "SHALL:handle"
},
{
"url": "actor",
"valueCanonical": "http://hl7.eu/fhir/ig/idea4rc/actor-headneck-i4rc"
}
],
"url": "http://hl7.org/fhir/StructureDefinition/obligation"
}
],
"path": "AdverseEvent.adverseEventType",
"short": "Adverse event type (CTCAE Term) (M)",
"definition": "the Common Terminology Criteria for Adverse Events (CTCAE) is used to identify the adverse events. It includes details of the adverse event type and grade \nOBSERVATION or CONDITION (check)",
"min": 1,
"max": "*",
"type": [
{
"code": "CodeableConcept"
}
]
},
{
"id": "AdverseEvent.adverseEventStartingDate",
"extension": [
{
"extension": [
{
"url": "code",
"valueCode": "SHALL:handle"
},
{
"url": "actor",
"valueCanonical": "http://hl7.eu/fhir/ig/idea4rc/actor-headneck-i4rc"
}
],
"url": "http://hl7.org/fhir/StructureDefinition/obligation"
}
],
"path": "AdverseEvent.adverseEventStartingDate",
"short": "Adverse event starting date (M)",
"definition": "specifies when adverse events begins \nOBSERVATION or CONDITION (check)",
"min": 1,
"max": "*",
"type": [
{
"code": "date"
}
]
},
{
"id": "AdverseEvent.adverseEventDuration",
"extension": [
{
"extension": [
{
"url": "code",
"valueCode": "SHALL:handle"
},
{
"url": "actor",
"valueCanonical": "http://hl7.eu/fhir/ig/idea4rc/actor-headneck-i4rc"
}
],
"url": "http://hl7.org/fhir/StructureDefinition/obligation"
}
],
"path": "AdverseEvent.adverseEventDuration",
"short": "Adverse event duration (M)",
"definition": "specifies the duration of the adverse event \nOBSERVATION or CONDITION (check)\n\nAdverse Events in OMOP ar standard conditions or observations and duration must be derived from that data\n\nhttps://forums.ohdsi.org/t/mapping-adverse-event-data-to-omop-and-to-fhir/15373",
"comment": "Less than one week - 2000100050\nMore than one week but less than a month - 2000100051\nMore than a month but less than 3 months - 2000100052\nMore than 3 months - 2000100053",
"min": 1,
"max": "*",
"type": [
{
"code": "CodeableConcept"
}
]
}
]
}
}
AdverseEvent 
treatmentReference[x] 
treatmentReferenceSystemicTreatment
adverseEventStartingDate 
FHIR