Release 5 Ballot

This page is part of the FHIR Specification (v5.0.0-ballot: R5 Ballot - see ballot notes). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions . Page versions: R4B R4 R3

Example CodeSystem/adverse-event-causality-assess (XML)

Patient Care Work GroupMaturity Level: N/AStandards Status: Informative

Raw XML (canonical form + also see XML Format Specification)

Definition for Code SystemAdverseEventCausalityAssessment

<?xml version="1.0" encoding="UTF-8"?>

<CodeSystem xmlns="http://hl7.org/fhir">
  <id value="adverse-event-causality-assess"/> 
  <meta> 
    <lastUpdated value="2022-09-10T04:52:37.223+10:00"/> 
    <profile value="http://hl7.org/fhir/StructureDefinition/shareablecodesystem"/> 
  </meta> 
  <text> 
    <status value="generated"/> 
    <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> 
  </text> 
  <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-wg">
    <valueCode value="pc"/> 
  </extension> 
  <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status">
    <valueCode value="draft"/> 
  </extension> 
  <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm">
    <valueInteger value="1"/> 
  </extension> 
  <url value="http://terminology.hl7.org/CodeSystem/adverse-event-causality-assess"/> 
  <identifier> 
    <system value="urn:ietf:rfc:3986"/> 
    <value value="urn:oid:2.16.840.1.113883.4.642.4.1254"/> 
  </identifier> 
  <version value="5.0.0-ballot"/> 
  <name value="AdverseEventCausalityAssessment"/> 
  <title value="AdverseEventCausalityAssessment"/> 
  <status value="draft"/> 
  <experimental value="false"/> 
  <date value="2020-12-28T16:55:11+11:00"/> 
  <publisher value="HL7 (FHIR Project)"/> 
  <contact> 
    <telecom> 
      <system value="url"/> 
      <value value="http://hl7.org/fhir"/> 
    </telecom> 
    <telecom> 
      <system value="email"/> 
      <value value="fhir@lists.hl7.org"/> 
    </telecom> 
  </contact> 
  <description value="Codes for the assessment of whether the entity caused the event."/> 
  <caseSensitive value="true"/> 
  <valueSet value="http://hl7.org/fhir/ValueSet/adverse-event-causality-assess"/> 
  <content value="complete"/> 
  <concept> 
    <code value="certain"/> 
    <display value="Certain"/> 
    <definition value="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."/> 
  </concept> 
  <concept> 
    <code value="probably-likely"/> 
    <display value="Probably/Likely"/> 
    <definition value="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."/> 
  </concept> 
  <concept> 
    <code value="possible"/> 
    <display value="Possible"/> 
    <definition value="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."/> 
  </concept> 
  <concept> 
    <code value="unlikely"/> 
    <display value="Unlikely"/> 
    <definition value="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."/> 
  </concept> 
  <concept> 
    <code value="conditional-classified"/> 
    <display value="Conditional/Classified"/> 
    <definition value="i) Event or laboratory test abnormality; ii) More data for proper assessment needed;
     or iii) Additional data under examination."/> 
  </concept> 
  <concept> 
    <code value="unassessable-unclassifiable"/> 
    <display value="Unassessable/Unclassifiable"/> 
    <definition value="i) Report suggesting an adverse reaction; ii) Cannot be judged because information
     is insufficient or contradictory; or iii) Data cannot be supplemented or verified."/> 
  </concept> 
</CodeSystem> 

Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.