AdverseEvent

Actual or potential/avoided event causing unintended physical injury resulting from or contributed to by medical care, a research study or other healthcare setting factors that requires additional monitoring, treatment, or hospitalization, or that results in death.

These interaction paths describe standard FHIR R4 patterns. Availability can depend on the API capabilities enabled for your Ovok project.

Interaction	Method	Path
Read	GET	/fhir/R4/AdverseEvent/[id]
Vread	GET	/fhir/R4/AdverseEvent/[id]/_history/[vid]
Update	PUT	/fhir/R4/AdverseEvent/[id]
Patch	PATCH	/fhir/R4/AdverseEvent/[id]
Delete	DELETE	/fhir/R4/AdverseEvent/[id]
Create	POST	/fhir/R4/AdverseEvent
Search	GET	/fhir/R4/AdverseEvent
History	GET	/fhir/R4/AdverseEvent/[id]/_history

Top-level elements

Element	Type	Cardinality	Description
id	string	0..1	Logical id of this artifact
meta	Meta	0..1	Metadata about the resource
implicitRules	uri	0..1	A set of rules under which this content was created
language	code	0..1	Language of the resource content
text	Narrative	0..1	Text summary of the resource, for human interpretation
contained	Resource	0..*	Contained, inline Resources
extension	Extension	0..*	Additional content defined by implementations
modifierExtension	Extension	0..*	Extensions that cannot be ignored
identifier	Identifier	0..1	Business identifier for the event
actuality	code	1..1	actual | potential
category	CodeableConcept	0..*	product-problem | product-quality | product-use-error | wrong-dose | incorrect-prescribing-information | wrong-technique | wrong-route-of-administration | wrong-rate | wrong-duration | wrong-time | expired-drug | medical-device-use-error | problem-different-manufacturer | unsafe-physical-environment
event	CodeableConcept	0..1	Type of the event itself in relation to the subject
subject	Reference	1..1	Subject impacted by event
encounter	Reference	0..1	Encounter created as part of
date	dateTime	0..1	When the event occurred
detected	dateTime	0..1	When the event was detected
recordedDate	dateTime	0..1	When the event was recorded
resultingCondition	Reference	0..*	Effect on the subject due to this event
location	Reference	0..1	Location where adverse event occurred
seriousness	CodeableConcept	0..1	Seriousness of the event
severity	CodeableConcept	0..1	mild | moderate | severe
outcome	CodeableConcept	0..1	resolved | recovering | ongoing | resolvedWithSequelae | fatal | unknown
recorder	Reference	0..1	Who recorded the adverse event
contributor	Reference	0..*	Who was involved in the adverse event or the potential adverse event
suspectEntity	BackboneElement	0..*	The suspected agent causing the adverse event
subjectMedicalHistory	Reference	0..*	AdverseEvent.subjectMedicalHistory
referenceDocument	Reference	0..*	AdverseEvent.referenceDocument
study	Reference	0..*	AdverseEvent.study

Resource-specific search parameters

Parameter	Type	Description
actuality	token	actual | potential
category	token	product-problem | product-quality | product-use-error | wrong-dose | incorrect-prescribing-information | wrong-technique | wrong-route-of-administration | wrong-rate | wrong-duration | wrong-time | expired-drug | medical-device-use-error | problem-different-manufacturer | unsafe-physical-environment
date	date	When the event occurred
event	token	Type of the event itself in relation to the subject
location	reference	Location where adverse event occurred
recorder	reference	Who recorded the adverse event
resultingcondition	reference	Effect on the subject due to this event
seriousness	token	Seriousness of the event
severity	token	mild | moderate | severe
study	reference	AdverseEvent.study
subject	reference	Subject impacted by event
substance	reference	Refers to the specific entity that caused the adverse event

Reference

Official FHIR R4 spec: AdverseEvent.
Maturity: Draft (FMM 0).