This page is part of the HL7 Terminology (v5.1.0: Release) based on FHIR R4. The current version which supercedes this version is 5.2.0. For a full list of available versions, see the Directory of published versions 
: AdverseEventCausalityAssessment - JSON Representation
Raw json | Download
{
"resourceType" : "CodeSystem",
"id" : "adverse-event-causality-assess",
"meta" : {
"lastUpdated" : "2020-04-09T21:10:28.568+00:00"
},
"text" : {
"status" : "generated",
"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p>This 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>"
},
"extension" : [
{
"url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg",
"valueCode" : "pc"
},
{
"url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm",
"valueInteger" : 1
}
],
"url" : "http://terminology.hl7.org/CodeSystem/adverse-event-causality-assess",
"identifier" : [
{
"system" : "urn:ietf:rfc:3986",
"value" : "urn:oid:2.16.840.1.113883.4.642.1.1254"
}
],
"version" : "0.1.0",
"name" : "AdverseEventCausalityAssessment",
"title" : "AdverseEventCausalityAssessment",
"status" : "draft",
"experimental" : false,
"date" : "2020-04-09T21:10:28+00:00",
"publisher" : "HL7 (FHIR Project)",
"contact" : [
{
"telecom" : [
{
"system" : "url",
"value" : "http://hl7.org/fhir"
},
{
"system" : "email",
"value" : "fhir@lists.hl7.org"
}
]
}
],
"description" : "Codes for the assessment of whether the entity caused the event.",
"caseSensitive" : true,
"valueSet" : "http://terminology.hl7.org/ValueSet/adverse-event-causality-assess",
"content" : "complete",
"concept" : [
{
"code" : "certain",
"display" : "Certain",
"definition" : "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."
},
{
"code" : "probably-likely",
"display" : "Probably/Likely",
"definition" : "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."
},
{
"code" : "possible",
"display" : "Possible",
"definition" : "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."
},
{
"code" : "unlikely",
"display" : "Unlikely",
"definition" : "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."
},
{
"code" : "conditional-classified",
"display" : "Conditional/Classified",
"definition" : "i) Event or laboratory test abnormality; ii) More data for proper assessment needed; or iii) Additional data under examination."
},
{
"code" : "unassessable-unclassifiable",
"display" : "Unassessable/Unclassifiable",
"definition" : "i) Report suggesting an adverse reaction; ii) Cannot be judged because information is insufficient or contradictory; or iii) Data cannot be supplemented or verified."
}
]
}
|
Propose a change