AdverseEvent (11)

#NameSourceVerDescription
1Adverse Event Clinical Carehl7.fhir.uv.adverseeventclinicalcare#currentR5A profile of AdverseEvent for Clinical care, such as in incident reporting.
2Adverse Event Clinical Researchhl7.fhir.uv.ae-research-backport-ig#currentR4An example profile of AdverseEvent for Research reporting.
3Adverse Event Clinical Researchhl7.fhir.uv.ae-research-ig#currentR5An example profile of AdverseEvent for Research reporting.
4CDMH AdverseEventhl7.fhir.us.cdmh#currentR4This is the AdverseEvent Resource profile for the IG.
5CTC Adverse Eventhl7.fhir.us.pedcan#currentR4Profile of adverse event, using Common Terminology Criteria (CTC).
6CTC Adverse Eventhl7.fhir.us.ctcae#currentR4Profile of adverse event, using Common Terminology Criteria (CTC).
7ICSR Adverse Eventhl7.fhir.us.icsr-ae-reporting#currentR4The fields needed to submit an AdverseEvent for a ICSR Report.
8QICore AdverseEventhl7.fhir.us.qicore#currentR4An adverse event is an untoward occurrence during treatment that should be reported, for example, to a clinical study sponsor or safety oversight organization. AEs include reportable serious medical errors such as those defined by National Quality Forum (see http://www.qualityforum.org/Topics/ SREs/List_of_SREs.aspx), and Patient Safety Healthcare Events as defined by AHRQ. Some AEs can involve conditions such as "recurring headaches" but others do not, such as accidental falls, surgical errors, sexual abuse of patient, and sudden death. An adverse event can also be an unsafe condition that increases the probability of a patient safety event, and near-misses. An adverse event can be caused by exposure to some agent (e.g., a medication, immunization, food, or environmental agent). An adverse reaction can range from a mild reaction, such as a harmless rash to a severe and life-threatening condition. They can occur immediately or develop over time. For example, a patient may develop a rash after taking a particular medication.
9Radiotherapy Adverse Eventhl7.fhir.us.codex-radiation-therapy#currentR4A Radiotherapy Adverse Event is an adverse event resulting from radiation toxicity. This profile is based on the work of the [Vulcan project](http://www.hl7.org/vulcan/). Future versions of this IG should reference adverse event profiles from Vulcan, once they are published. The current profile is inspired by the work of Vulcan and Common Terminology Criteria (CTC) Adverse Event (CTCAE).
10Transfusion Adverse Eventhl7.fhir.us.icsr-ae-reporting#currentR4ICSR Adverse Event with a value set of transfusion-related events
11Vaccination Adverse Eventhl7.fhir.us.icsr-ae-reporting#currentR4ICSR Adverse Event with a value set of vaccination-related events
1 2 3 4 5 6 7 8 9 10 11
AdverseEvent I I D I I
AdverseEvent.contributor
AdverseEvent.date C
AdverseEvent.date.extension S C (3)
AdverseEvent.referenceDocument C
AdverseEvent.subjectMedicalHistory C
AdverseEvent.severity C D C
AdverseEvent.resultingCondition C
AdverseEvent.event D B M C B M C B M C C B M C D B M B M B M
AdverseEvent.event.text D D D
AdverseEvent.event.coding C D C D C
AdverseEvent.event.coding.system F
AdverseEvent.event.coding.display D D
AdverseEvent.event.coding.code D D
AdverseEvent.event.coding.version D D
AdverseEvent.meta
AdverseEvent.implicitRules
AdverseEvent.language
AdverseEvent.text
AdverseEvent.contained
AdverseEvent.extension S C D (14) S C (4) S C B M (2) S C (4) S C (6) S C (2) S C (2)
AdverseEvent.modifierExtension S C D B M (2)
AdverseEvent.identifier
AdverseEvent.status
AdverseEvent.actuality F F F F F F
AdverseEvent.category
AdverseEvent.code
AdverseEvent.subject C C
AdverseEvent.encounter
AdverseEvent.occurrence[x]
AdverseEvent.detected
AdverseEvent.recordedDate C
AdverseEvent.resultingEffect D
AdverseEvent.location
AdverseEvent.seriousness C C B M C B M B M B M C B M
AdverseEvent.seriousness.extension S C
AdverseEvent.outcome C B M C B M
AdverseEvent.recorder
AdverseEvent.participant
AdverseEvent.participant.extension
AdverseEvent.participant.modifierExtension
AdverseEvent.participant.function
AdverseEvent.participant.actor
AdverseEvent.study C C C
AdverseEvent.expectedInResearchStudy C
AdverseEvent.suspectEntity C C C S C (2) S C (2)
AdverseEvent.suspectEntity.instance
AdverseEvent.suspectEntity.extension
AdverseEvent.suspectEntity.modifierExtension
AdverseEvent.suspectEntity.instance[x]
AdverseEvent.suspectEntity.causality C C C C
AdverseEvent.suspectEntity.causality.productRelatedness C
AdverseEvent.suspectEntity.causality.assessment B M B M
AdverseEvent.suspectEntity.causality.assessment.text
AdverseEvent.suspectEntity.causality.extension S C B M (5)
AdverseEvent.suspectEntity.causality.modifierExtension
AdverseEvent.suspectEntity.causality.assessmentMethod B M
AdverseEvent.suspectEntity.causality.entityRelatedness B M
AdverseEvent.suspectEntity.causality.author
AdverseEvent.contributingFactor
AdverseEvent.contributingFactor.extension
AdverseEvent.contributingFactor.modifierExtension
AdverseEvent.contributingFactor.item[x]
AdverseEvent.preventiveAction C
AdverseEvent.preventiveAction.extension
AdverseEvent.preventiveAction.modifierExtension
AdverseEvent.preventiveAction.item[x]
AdverseEvent.mitigatingAction
AdverseEvent.mitigatingAction.extension
AdverseEvent.mitigatingAction.modifierExtension
AdverseEvent.mitigatingAction.item[x]
AdverseEvent.supportingInfo
AdverseEvent.supportingInfo.extension
AdverseEvent.supportingInfo.modifierExtension
AdverseEvent.supportingInfo.item[x] B M
AdverseEvent.note
S: There is slicing defined in the element(s)
C: There is cardinality erstrictions defined in the element(s)
I: There is invariants defined in the element(s)
F: There is a fixed or pattern value defined in the element(s)
D: There is document provided in the element(s)
B: There is terminology bindings defined in the element(s)
M: At least one of the element(s) has must-support = true
(N): The number of elements if > 1

Produced 08 Sep 2023