<?xml version="1.0" encoding="UTF-8"?><MedicinalProductUndesirableEffect xmlns="http://hl7.org/fhir"><id value="51a7768e-79ec-46a5-91b0-c3eec0151e79"/><meta><versionId value="1"/><lastUpdated value="2022-02-17T17:34:55.009+08:00"/><tag><system value="http://terminology.hl7.org/CodeSystem/v3-ActReason"/><code value="HTEST"/><display value="test health data"/></tag></meta><symptomConditionEffect><coding><system value="http://ema.europa.eu/example/undesirableeffectassymptom-condition-effect"/><code value="Anaemia"/></coding><text value="Prevention of\nVTE in adult\npatients who have\nundergone\nelective hip or\nknee replacement\nsurgery (VTEp)"/></symptomConditionEffect><classification><coding><system value="http://ema.europa.eu/example/symptom-condition-effectclassification"/><code value="Bloodandlymphaticsystemdisorders"/></coding></classification><frequencyOfOccurrence><coding><system value="http://ema.europa.eu/example/frequencyofoccurrence"/><code value="Common"/></coding></frequencyOfOccurrence></MedicinalProductUndesirableEffect>