DSTU2 QA Preview

This page is part of the FHIR Specification (v1.0.0: DSTU 2 Ballot 3). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions

F.?? QICore-AdverseEvent

F.??.1 Content

Profiles:
QICore-AdverseEventAny untoward occurrence during treatment that must be reported.
Extensions:
qicore-adverseevent-causeThe possible cause(s) of the adverse event :

Details about causes for this adverse event. Note that causes may not always exist or be available.

qicore-adverseevent-clinicalStudyRelated clinical study :

The NCT numbers of the clinical studies the patient participates in at the time of the adverse event (if available).

qicore-adverseevent-typePrimary code :

The adverse event experienced by the patient (primary code).

qicore-adverseevent-didNotOccurIndicates if the adverse event was absent :

When true, the resource implies that the adverse event did NOT occur during the stated time period. If true, the severity should not be specified, and the certainty value will be ignored.

qicore-adverseevent-periodEffective time period :

The time period during which the adverse event occurred.

qicore-adverseevent-severityseverity :

The severity of the adverse event.

qicore-adverseevent-relatedRelated item :

A condition or intolerance that is related to this adverse event.