Release 4B Snapshot #1

This page is part of the FHIR Specification v4.3.0-snapshot1: R4B Snapshot to support the Jan 2022 Connectathon. About the R4B version of FHIR. The current officially released version is 4.3.0. For a full list of available versions, see the Directory of published versions . Page versions: R4B R4 R3

4.3.14.421 Code System http://terminology.hl7.org/CodeSystem/adverse-event-causality-assess

Patient Care Work Group Maturity Level: 1Draft Use Context: Any

This is a code system defined by the FHIR project.

Summary

Defining URL:http://terminology.hl7.org/CodeSystem/adverse-event-causality-assess
Version:4.3.0-snapshot1
Name:AdverseEventCausalityAssessment
Title:AdverseEventCausalityAssessment
Definition:

Codes for the assessment of whether the entity caused the event.

Committee:Patient Care Work Group
OID:2.16.840.1.113883.4.642.4.1254 (for OID based terminology systems)
Source ResourceXML / JSON

This Code system is used in the following value sets:

4.3.14.421.1 Content

4.3.14.421.2 AdverseEventCausalityAssessment

Codes for the assessment of whether the entity caused the event.

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

Code Display Definition
Certain Certain 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.
Probably-Likely Probably/Likely 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.
Possible Possible 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.
Unlikely Unlikely 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.
Conditional-Classified Conditional/Classified i) Event or laboratory test abnormality; ii) More data for proper assessment needed; or iii) Additional data under examination.
Unassessable-Unclassifiable Unassessable/Unclassifiable i) Report suggesting an adverse reaction; ii) Cannot be judged because information is insufficient or contradictory; or iii) Data cannot be supplemented or verified.

 

See the full registry of code systems defined as part of FHIR.

Explanation of the columns that may appear on this page:

LevelA 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