R4 Draft for Comment

This page is part of the FHIR Specification (v3.2.0: R4 Ballot 1). 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

4.2.12.841 Code System http://hl7.org/fhir/adverse-event-causality-assess

Vocabulary Work Group Maturity Level: 1Draft Use Context: Any

This is a code system defined by the FHIR project.

Summary

Defining URL:http://hl7.org/fhir/adverse-event-causality-assess
Name:AdverseEventCausalityAssessment
Definition:

TODO

Committee:Patient Care Work Group
OID:2.16.840.1.113883.4.642.1.841 (for OID based terminology systems)
Source ResourceXML / JSON

This Code system is used in the following value sets:

4.2.12.841.1 Content

4.2.12.841.2 AdverseEventCausalityAssessment

TODO

This code system http://hl7.org/fhir/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) 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 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 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) 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 iii) Data cannot be supplemented or verified

 

See the full registry of value sets defined as part of FHIR.

Explanation of the columns that may appear on this page:

LvlA few code lists that FHIR defines are hierarchical - each code is assigned a level. See Code System for further information.
SourceThe source of the definition of the code (when the value set draws in codes defined elsewhere)
CodeThe code (used as the code in the resource instance). If the code is in italics, this indicates that the code is not selectable ('Abstract')
DisplayThe display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application
DefinitionAn explanation of the meaning of the concept
CommentsAdditional notes about how to use the code