AdverseEventCausalityAssessment

AdverseEventCausalityAssessment

draftExtensions for Using Data Elements from FHIR R5 in FHIR R40.1.0complete6 concepts

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

Metadata

hl7.org/fhir
Canonical URL
http://terminology.hl7.org/CodeSystem/adverse-event-causality-assess
ID
adverse-event-causality-assess
Version
0.1.0
Publisher
Patient Care
Case Sensitive
Yes

Concepts (6)

CodeDisplayDefinition
certainCertaini) 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-likelyProbably/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; or iv) Re-challenge not required.
possiblePossiblei) 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.
unlikelyUnlikelyi) 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-classifiedConditional/Classifiedi) Event or laboratory test abnormality; ii) More data for proper assessment needed; or iii) Additional data under examination.
unassessable-unclassifiableUnassessable/Unclassifiablei) Report suggesting an adverse reaction; ii) Cannot be judged because information is insufficient or contradictory; or iii) Data cannot be supplemented or verified.