R6 Ballot (3rd Draft) FHIR CI-Build

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Example ClinicalUseDefinition/example-undesirable (XML)

Maturity Level : N/A
Responsible Owner: Biomedical Research and Regulation Work Group Standards Status : Informative Compartments : No defined compartments

Raw XML ( canonical form + also see XML Format Specification )

Undesirable effect example (id = "example-undesirable") 

<?xml version="1.0" encoding="UTF-8"?>

<ClinicalUseDefinition xmlns="http://hl7.org/fhir">
  <id value="example-undesirable"/> 
  <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-wg">
    <valueCode value="brr"/> 
  </extension> 
  <!--   common side effect   -->
  <type value="undesirable-effect"/> 
  <subject> 
    

    <reference> 
      <reference value="MedicinalProductDefinition/example"/> 
    </reference> 
  </subject> 
  <undesirableEffect> 
    <symptomConditionEffect> 
      <concept> 
        <coding> 
          <system value="http://ema.europa.eu/example/undesirableeffectassymptom-condition-effect"/> 
          <code value="Anaemia"/> 
        </coding> 
      </concept> 
    </symptomConditionEffect> 
    <classification> 
      <coding> 
        <system value="http://ema.europa.eu/example/symptom-condition-effectclassification"/> 
        <code value="Blood-and-lymphatic-system-disorders"/> 
      </coding> 
    </classification> 
    <frequencyOfOccurrence> 
      <coding> 
        <system value="http://ema.europa.eu/example/frequencyofoccurrence"/> 
        <code value="Common"/> 
      </coding> 
    </frequencyOfOccurrence> 
  </undesirableEffect> 


</

ClinicalUseDefinition

>

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.