HL7 Terminology (THO), published by HL7 International - Vocabulary Work Group. This guide is not an authorized publication; it is the continuous build for version 6.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/UTG/ and changes regularly. See the Directory of published versions
: AdverseEventCausalityAssessment - TTL Representation
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@prefix fhir: <http://hl7.org/fhir/> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
# - resource -------------------------------------------------------------------
a fhir:CodeSystem ;
fhir:nodeRole fhir:treeRoot ;
fhir:id [ fhir:v "adverse-event-causality-assess"] ; #
fhir:meta [
fhir:lastUpdated [ fhir:v "2024-04-24T00:00:00+00:00"^^xsd:dateTime ]
] ; #
fhir:text [
fhir:status [ fhir:v "generated" ] ;
fhir:div "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: CodeSystem adverse-event-causality-assess</b></p><a name=\"adverse-event-causality-assess\"> </a><a name=\"hcadverse-event-causality-assess\"> </a><a name=\"adverse-event-causality-assess-en-US\"> </a><div style=\"display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%\"><p style=\"margin-bottom: 0px\">Last updated: 2024-04-24 00:00:00+0000</p></div><p>This case-sensitive code system <code>http://terminology.hl7.org/CodeSystem/adverse-event-causality-assess</code> defines the following codes:</p><table class=\"codes\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td><td><b>Definition</b></td></tr><tr><td style=\"white-space:nowrap\">certain<a name=\"adverse-event-causality-assess-certain\"> </a></td><td>Certain</td><td>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.</td></tr><tr><td style=\"white-space:nowrap\">probably-likely<a name=\"adverse-event-causality-assess-probably-likely\"> </a></td><td>Probably/Likely</td><td>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.</td></tr><tr><td style=\"white-space:nowrap\">possible<a name=\"adverse-event-causality-assess-possible\"> </a></td><td>Possible</td><td>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.</td></tr><tr><td style=\"white-space:nowrap\">unlikely<a name=\"adverse-event-causality-assess-unlikely\"> </a></td><td>Unlikely</td><td>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.</td></tr><tr><td style=\"white-space:nowrap\">conditional-classified<a name=\"adverse-event-causality-assess-conditional-classified\"> </a></td><td>Conditional/Classified</td><td>i) Event or laboratory test abnormality; ii) More data for proper assessment needed; or iii) Additional data under examination.</td></tr><tr><td style=\"white-space:nowrap\">unassessable-unclassifiable<a name=\"adverse-event-causality-assess-unassessable-unclassifiable\"> </a></td><td>Unassessable/Unclassifiable</td><td>i) Report suggesting an adverse reaction; ii) Cannot be judged because information is insufficient or contradictory; or iii) Data cannot be supplemented or verified.</td></tr></table></div>"
] ; #
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 "1.0.1"] ; #
fhir:name [ fhir:v "AdverseEventCausalityAssessment"] ; #
fhir:title [ fhir:v "AdverseEventCausalityAssessment"] ; #
fhir:status [ fhir:v "active"] ; #
fhir:experimental [ fhir:v "false"^^xsd:boolean] ; #
fhir:date [ fhir:v "2024-04-24T00:00:00+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 <http://terminology.hl7.org/ValueSet/adverse-event-causality-assess>
] ; #
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." ]
] ) . #
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