{"resourceType":"CodeSystem","id":"v2-0252","meta":{"profile":["http://hl7.org/fhir/StructureDefinition/shareablecodesystem"]},"language":"en","extension":[{"url":"http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status","valueCode":"external"},{"url":"http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm","valueInteger":0}],"url":"http://terminology.hl7.org/CodeSystem/v2-0252","identifier":[{"system":"urn:ietf:rfc:3986","value":"urn:oid:2.16.840.1.113883.18.147"}],"version":"2.9","name":"v2.0252","title":"v2 Causality Observations","status":"active","experimental":false,"publisher":"HL7, Inc","contact":[{"telecom":[{"system":"url","value":"http://hl7.org"}]}],"description":"FHIR Value set/code system definition for HL7 v2 table 0252 ( Causality Observations)","content":"complete","concept":[{"code":"AW","display":"Abatement of event after product withdrawn","designation":[{"language":"nl","use":{"system":"http://terminology.hl7.org/CodeSystem/designation-usage","code":"display"},"value":"Vermindering gebeurtenis na terugtrekken product"}]},{"code":"BE","display":"Event recurred after product reintroduced","designation":[{"language":"nl","use":{"system":"http://terminology.hl7.org/CodeSystem/designation-usage","code":"display"},"value":"Gebeurtenis trad opnieuw op na herintroductie product"}]},{"code":"DR","display":"Dose response observed","designation":[{"language":"nl","use":{"system":"http://terminology.hl7.org/CodeSystem/designation-usage","code":"display"},"value":"Dosis reactie geobserveerd"}]},{"code":"EX","display":"Alternative explanations for the event available","designation":[{"language":"nl","use":{"system":"http://terminology.hl7.org/CodeSystem/designation-usage","code":"display"},"value":"Alternatieve verklaringen voor gebeurtenis beschikbaar"}]},{"code":"IN","display":"Event occurred after product introduced","designation":[{"language":"nl","use":{"system":"http://terminology.hl7.org/CodeSystem/designation-usage","code":"display"},"value":"Gebeurtenis trad op na introductie product"}]},{"code":"LI","display":"Literature reports association of product with event","designation":[{"language":"nl","use":{"system":"http://terminology.hl7.org/CodeSystem/designation-usage","code":"display"},"value":"Literatuur vermeldt koppeling van product met gebeurtenis"}]},{"code":"OE","display":"Occurrence of event was confirmed by objective evidence","designation":[{"language":"nl","use":{"system":"http://terminology.hl7.org/CodeSystem/designation-usage","code":"display"},"value":"Optreden van gebeurtenis is bevestigd door objectief bewijs"}]},{"code":"OT","display":"Other","designation":[{"language":"nl","use":{"system":"http://terminology.hl7.org/CodeSystem/designation-usage","code":"display"},"value":"Anders"}]},{"code":"PL","display":"Effect observed when patient receives placebo","designation":[{"language":"nl","use":{"system":"http://terminology.hl7.org/CodeSystem/designation-usage","code":"display"},"value":"Effect geobserveerd wanneer patiënt placebo krijgt"}]},{"code":"SE","display":"Similar events in past for this patient","designation":[{"language":"nl","use":{"system":"http://terminology.hl7.org/CodeSystem/designation-usage","code":"display"},"value":"Vergelijkbare gebeurtenissen in verleden voor deze patiënt"}]},{"code":"TC","display":"Toxic levels of product documented in blood or body fluids","designation":[{"language":"nl","use":{"system":"http://terminology.hl7.org/CodeSystem/designation-usage","code":"display"},"value":"Toxische niveaus van product gedocumenteerd in bloed of lichaamssappen"}]}]}