This page is part of the Electronic Medicinal Product Information (ePI) FHIR Implementation Guide (v1.0.0-ballot: STU1 Ballot 1) based on FHIR v5.0.0-ballot. . For a full list of available versions, see the Directory of published versions
: warninghypotension - TTL Representation
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@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 -------------------------------------------------------------------
a fhir:ClinicalUseDefinition;
fhir:nodeRole fhir:treeRoot;
fhir:Resource.id [ fhir:value "ac21a804-cafa-41ff-b644-a14c8003edeb"]; #
fhir:Resource.meta [
fhir:Meta.profile [
fhir:value "http://hl7.org/fhir/uv/emedicinal-product-info/StructureDefinition/ClinicalUseDefinition-warning-uv-epi";
fhir:index 0;
fhir:link <http://hl7.org/fhir/uv/emedicinal-product-info/StructureDefinition/ClinicalUseDefinition-warning-uv-epi> ]
]; #
fhir:DomainResource.text [
fhir:Narrative.status [ fhir:value "generated" ];
fhir:Narrative.div "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p><b>Generated Narrative: ClinicalUseDefinition</b><a name=\"ac21a804-cafa-41ff-b644-a14c8003edeb\"> </a></p><div style=\"display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%\"><p style=\"margin-bottom: 0px\">Resource ClinicalUseDefinition "ac21a804-cafa-41ff-b644-a14c8003edeb" </p><p style=\"margin-bottom: 0px\">Profile: <a href=\"StructureDefinition-ClinicalUseDefinition-warning-uv-epi.html\">ClinicalUseDefinition Warning (ePI)</a></p></div><p><b>identifier</b>: id: hypotension (use: OFFICIAL)</p><p><b>type</b>: warning</p><p><b>subject</b>: <a href=\"MedicinalProductDefinition-800a51a2-d81d-49a4-a4eb-f2417d301837.html\">MedicinalProductDefinition/800a51a2-d81d-49a4-a4eb-f2417d301837</a></p><h3>Warnings</h3><table class=\"grid\"><tr><td>-</td><td><b>Description</b></td></tr><tr><td>*</td><td>Intravascular volume depletion: symptomatic hypotension, especially after the first dose, may occur in patients who are volume and/or sodium depleted by vigorous diuretic therapy, dietary salt restriction, diarrhoea or vomiting. Such conditions should be corrected before the administration of cava.</td></tr></table></div>"
]; #
fhir:ClinicalUseDefinition.identifier [
fhir:index 0;
fhir:Identifier.use [ fhir:value "official" ];
fhir:Identifier.system [ fhir:value "https://spor.ema.europa.eu/rmswi#" ];
fhir:Identifier.value [ fhir:value "hypotension" ]
]; #
fhir:ClinicalUseDefinition.type [ fhir:value "warning"]; #
fhir:ClinicalUseDefinition.subject [
fhir:index 0;
fhir:Reference.reference [ fhir:value "MedicinalProductDefinition/800a51a2-d81d-49a4-a4eb-f2417d301837" ]
]; #
fhir:ClinicalUseDefinition.warning [
fhir:ClinicalUseDefinition.warning.description [ fhir:value "Intravascular volume depletion: symptomatic hypotension, especially after the first dose, may occur in patients who are volume and/or sodium depleted by vigorous diuretic therapy, dietary salt restriction, diarrhoea or vomiting. Such conditions should be corrected before the administration of cava." ]
]. #
# - ontology header ------------------------------------------------------------
a owl:Ontology;
owl:imports fhir:fhir.ttl.