This page is part of the FHIR Specification (v4.0.1: R4 - Mixed Normative and STU) in it's permanent home (it will always be available at this URL). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions
Biomedical Research and Regulation Work Group | Maturity Level: N/A | Standards Status: Informative | Compartments: Not linked to any defined compartments |
Raw Turtle (+ also see Turtle/RDF Format Specification)
Example of medicinalproductundesirableeffect
@prefix fhir: <http://hl7.org/fhir/> . @prefix owl: <http://www.w3.org/2002/07/owl#> . @prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> . @prefix xsd: <http://www.w3.org/2001/XMLSchema#> . # - resource ------------------------------------------------------------------- <http://hl7.org/fhir/MedicinalProductUndesirableEffect/example> a fhir:MedicinalProductUndesirableEffect; fhir:nodeRole fhir:treeRoot; fhir:Resource.id [ fhir:value "example"]; fhir:DomainResource.text [ fhir:Narrative.status [ fhir:value "generated" ]; fhir:Narrative.div "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p><b>Generated Narrative with Details</b></p><p><b>id</b>: example</p><p><b>symptomConditionEffect</b>: Prevention of\\nVTE in adult\\npatients who have\\nundergone\\nelective hip or\\nknee replacement\\nsurgery (VTEp) <span>(Details : {http://ema.europa.eu/example/undesirableeffectassymptom-condition-effect code 'Anaemia' = 'Anaemia)</span></p><p><b>classification</b>: Bloodandlymphaticsystemdisorders <span>(Details : {http://ema.europa.eu/example/symptom-condition-effectclassification code 'Bloodandlymphaticsystemdisorders' = 'Bloodandlymphaticsystemdisorders)</span></p><p><b>frequencyOfOccurrence</b>: Common <span>(Details : {http://ema.europa.eu/example/frequencyofoccurrence code 'Common' = 'Common)</span></p></div>" ]; fhir:MedicinalProductUndesirableEffect.symptomConditionEffect [ fhir:CodeableConcept.coding [ fhir:index 0; fhir:Coding.system [ fhir:value "http://ema.europa.eu/example/undesirableeffectassymptom-condition-effect" ]; fhir:Coding.code [ fhir:value "Anaemia" ] ]; fhir:CodeableConcept.text [ fhir:value "Prevention of\\nVTE in adult\\npatients who have\\nundergone\\nelective hip or\\nknee replacement\\nsurgery (VTEp)" ] ]; fhir:MedicinalProductUndesirableEffect.classification [ fhir:CodeableConcept.coding [ fhir:index 0; fhir:Coding.system [ fhir:value "http://ema.europa.eu/example/symptom-condition-effectclassification" ]; fhir:Coding.code [ fhir:value "Bloodandlymphaticsystemdisorders" ] ] ]; fhir:MedicinalProductUndesirableEffect.frequencyOfOccurrence [ fhir:CodeableConcept.coding [ fhir:index 0; fhir:Coding.system [ fhir:value "http://ema.europa.eu/example/frequencyofoccurrence" ]; fhir:Coding.code [ fhir:value "Common" ] ] ] . # - ontology header ------------------------------------------------------------ <http://hl7.org/fhir/MedicinalProductUndesirableEffect/example.ttl> a owl:Ontology; owl:imports fhir:fhir.ttl; owl:versionIRI <http://build.fhir.org/MedicinalProductUndesirableEffect/example.ttl> . # -------------------------------------------------------------------------------------
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.