@prefix fhir: . @prefix owl: . @prefix rdfs: . @prefix xsd: . # - resource ------------------------------------------------------------------- a fhir:CodeSystem ; fhir:nodeRole fhir:treeRoot ; fhir:id [ fhir:v "adverse-event-causality-assess"] ; # fhir:meta [ fhir:lastUpdated [ fhir:v "2020-04-09T21:10:28.568+00:00"^^xsd:dateTime ] ] ; # fhir:text [ fhir:status [ fhir:v "generated" ] ; fhir:div "

This case-sensitive code system http://terminology.hl7.org/CodeSystem/adverse-event-causality-assess defines the following codes:

CodeDisplayDefinition
certain Certaini) Event or laboratory test abnormality, with plausible time relationship to drug intake; ii) Cannot be explained by disease or other drugs; iii) Response to withdrawal plausible (pharmacologically, pathologically); iv) Event definitive pharmacologically or phenomenologically (i.e. an objective and specific medical disorder or a recognized pharmacological phenomenon); or v) Re-challenge satisfactory, if necessary.
probably-likely Probably/Likelyi) Event or laboratory test abnormality, with reasonable time relationship to drug intake; ii) Unlikely to be attributed to disease or other drugs; iii) Response to withdrawal clinically reasonable; or iv) Re-challenge not required.
possible Possiblei) Event or laboratory test abnormality, with reasonable time relationship to drug intake; ii) Could also be explained by disease or other drugs; or iii) Information on drug withdrawal may be lacking or unclear.
unlikely Unlikelyi) Event or laboratory test abnormality, with a time to drug intake that makes a relationship improbable (but not impossible); or ii) Disease or other drugs provide plausible explanations.
conditional-classified Conditional/Classifiedi) Event or laboratory test abnormality; ii) More data for proper assessment needed; or iii) Additional data under examination.
unassessable-unclassifiable Unassessable/Unclassifiablei) Report suggesting an adverse reaction; ii) Cannot be judged because information is insufficient or contradictory; or iii) Data cannot be supplemented or verified.
" ] ; # fhir:extension ( [ fhir:url [ fhir:v "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg"^^xsd:anyURI ] ; fhir:value [ fhir:v "pc" ] ] [ fhir:url [ fhir:v "http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm"^^xsd:anyURI ] ; fhir:value [ fhir:v "1"^^xsd:integer ] ] ) ; # fhir:url [ fhir:v "http://terminology.hl7.org/CodeSystem/adverse-event-causality-assess"^^xsd:anyURI] ; # fhir:identifier ( [ fhir:system [ fhir:v "urn:ietf:rfc:3986"^^xsd:anyURI ] ; fhir:value [ fhir:v "urn:oid:2.16.840.1.113883.4.642.1.1254" ] ] ) ; # fhir:version [ fhir:v "1.0.0"] ; # fhir:name [ fhir:v "AdverseEventCausalityAssessment"] ; # fhir:title [ fhir:v "AdverseEventCausalityAssessment"] ; # fhir:status [ fhir:v "draft"] ; # fhir:experimental [ fhir:v "false"^^xsd:boolean] ; # fhir:date [ fhir:v "2020-04-09T21:10:28+00:00"^^xsd:dateTime] ; # fhir:publisher [ fhir:v "Health Level Seven International"] ; # fhir:contact ( [ fhir:telecom ( [ fhir:system [ fhir:v "url" ] ; fhir:value [ fhir:v "http://hl7.org" ] ] [ fhir:system [ fhir:v "email" ] ; fhir:value [ fhir:v "hq@HL7.org" ] ] ) ] ) ; # fhir:description [ fhir:v "Codes for the assessment of whether the entity caused the event."] ; # fhir:copyright [ fhir:v "This material derives from the HL7 Terminology (THO). THO is copyright ©1989+ Health Level Seven International and is made available under the CC0 designation. For more licensing information see: https://terminology.hl7.org/license"] ; # fhir:caseSensitive [ fhir:v "true"^^xsd:boolean] ; # fhir:valueSet [ fhir:v "http://terminology.hl7.org/ValueSet/adverse-event-causality-assess"^^xsd:anyURI ; fhir:link ] ; # fhir:content [ fhir:v "complete"] ; # fhir:concept ( [ fhir:code [ fhir:v "certain" ] ; fhir:display [ fhir:v "Certain" ] ; fhir:definition [ fhir:v "i) Event or laboratory test abnormality, with plausible time relationship to drug intake; ii) Cannot be explained by disease or other drugs; iii) Response to withdrawal plausible (pharmacologically, pathologically); iv) Event definitive pharmacologically or phenomenologically (i.e. an objective and specific medical disorder or a recognized pharmacological phenomenon); or v) Re-challenge satisfactory, if necessary." ] ] [ fhir:code [ fhir:v "probably-likely" ] ; fhir:display [ fhir:v "Probably/Likely" ] ; fhir:definition [ fhir:v "i) Event or laboratory test abnormality, with reasonable time relationship to drug intake; ii) Unlikely to be attributed to disease or other drugs; iii) Response to withdrawal clinically reasonable; or iv) Re-challenge not required." ] ] [ fhir:code [ fhir:v "possible" ] ; fhir:display [ fhir:v "Possible" ] ; fhir:definition [ fhir:v "i) Event or laboratory test abnormality, with reasonable time relationship to drug intake; ii) Could also be explained by disease or other drugs; or iii) Information on drug withdrawal may be lacking or unclear." ] ] [ fhir:code [ fhir:v "unlikely" ] ; fhir:display [ fhir:v "Unlikely" ] ; fhir:definition [ fhir:v "i) Event or laboratory test abnormality, with a time to drug intake that makes a relationship improbable (but not impossible); or ii) Disease or other drugs provide plausible explanations." ] ] [ fhir:code [ fhir:v "conditional-classified" ] ; fhir:display [ fhir:v "Conditional/Classified" ] ; fhir:definition [ fhir:v "i) Event or laboratory test abnormality; ii) More data for proper assessment needed; or iii) Additional data under examination." ] ] [ fhir:code [ fhir:v "unassessable-unclassifiable" ] ; fhir:display [ fhir:v "Unassessable/Unclassifiable" ] ; fhir:definition [ fhir:v "i) Report suggesting an adverse reaction; ii) Cannot be judged because information is insufficient or contradictory; or iii) Data cannot be supplemented or verified." ] ] ) . # # -------------------------------------------------------------------------------------