Integrated Campaign Registry (ICR) Implementation Guideunicef.fhir.icr · v0.1.0 · FHIR 4.0.1
Draft — this implementation guide is a working snapshot (v0.1.0) and its content may change without notice.
Code Systemv0.1.0·draft

ICR Adverse Event Causality

WHO/CIOMS causality classification of an adverse event following an intervention — intervention-neutral: covers AEFI (immunization) and MDA drug pharmacovigilance alike. Top-level WHO categories; immunization implementations may use WHO IMMZ.AdverseEvent's finer A1–A4 subtypes (espen-v3 / §17.2 C1).

Canonical
https://fhir.icr.unicef.org/CodeSystem/icr-adverse-event-causality-cs
Content
complete
Case sensitive
true
Experimental
false

Concepts (4)

4 shown
CodeDisplayDefinition
a-consistentA — Consistent causal associationConsistent causal association to the intervention (WHO category A; immunization subtypes A1 product, A2 quality defect, A3 administration error, A4 anxiety).
b-indeterminateB — IndeterminateIndeterminate: conflicting trends or insufficient evidence.
c-coincidentalC — Coincidental / inconsistentInconsistent causal association — coincidental, due to underlying/emerging condition or other exposure.
d-unclassifiableD — UnclassifiableUnclassifiable: insufficient information to assess.