DSTU2

This page is part of the FHIR Specification (v1.0.2: DSTU 2). 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.2.0 QICore-AdverseEvent

F.2.0.1 Content

Profiles:
QICore-AdverseEventAn incident, near miss, unsafe condition, or untoward occurrence during treatment.
Extensions:
qicore-adverseevent-typeWhat type of adverse event is being reported :

The type of adverse event, either an incident, near miss, or unsafe condition.

qicore-adverseevent-discoveryDateTimeThe date and time when the adverse event was discovered :

The date and time when the adverse event was discovered.

qicore-adverseevent-locationThe location of the adverse event :

The location where the event occurred or where the unsafe condition exists.

qicore-adverseevent-categoryThe category(s) of the healthcare event :

The categories associated with the event or unsafe condition.

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-reactionThe adverse reaction experienced by the patient :

The adverse reaction experienced by the patient.

qicore-adverseevent-periodTime period of adverse event :

The time period during which the adverse event occurred.

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-severityseverity :

The severity of the adverse event.

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.