This page is part of the Adverse Event Clinical Research R4 Backport (v1.0.1: STU 1) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions

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Extension: Adverse event caused subject to discontinue the study

Official URL: http://hl7.org/fhir/uv/ae-research-backport-ig/StructureDefinition/caused-subject-to-discontinue-study				Version: 1.0.1
Standards status: Trial-use			Maturity Level: 2	Computable Name: CausedSubjectToDiscontinueStudy

Indicates if the subject discontinued the study due to the adverse event.

Context of Use

This extension may be used on the following element(s):

• Element ID AdverseEvent

Usage info

Usage:

• Use this Extension: Adverse Event Clinical Research
• Examples for this Extension: AdverseEvent/AdverseEventFromProcedureNotStudyDrug, AdverseEvent/NonSeriousAdverseEventResearchStudyMed and AdverseEvent/SeriousAdverseEventResearchStudy

Formal Views of Extension Content

Description of Profiles, Differentials, Snapshots, and how the XML and JSON presentations work.

 

Other representations of profile: CSV, Excel, Schematron

Constraints

Id	Grade	Path(s)	Details	Requirements
ele-1	error	**ALL** elements	All FHIR elements must have a @value or children : hasValue() or (children().count() > id.count())
ext-1	error	**ALL** extensions	Must have either extensions or value[x], not both : extension.exists() != value.exists()