<?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>