Adverse Event Clinical Research R4 Backport, published by HL7 International / Biomedical Research and Regulation. This guide is not an authorized publication; it is the continuous build for version 1.0.1 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/fhir-ae-research-backport-ig/ and changes regularly. See the Directory of published versions
Generated Narrative: AdverseEvent
Resource AdverseEvent "adverse-event-compass-ex2"
Profile: Adverse Event Clinical Research
Resulting Effect: : Reference to Condition instance of Nausea that resolved
Supporting information relevant to the event
url
item
value: : Supporting info would have context such as an Reference to Condition instance of Nausea, where Condition.status is resolved.
Adverse Event Grade: Grade 1 Mild Adverse Event (NCI Thesaurus#C41338)
Participant
url
function
value: authenticator (ParticipationType#AUTHEN)
url
actor
value: Practitioner/practitioner-owen-oncologist " ONCOLOGIST"
Suspect Entity
url
instance
value: MedicationAdministration/medication-administration-kadcyla
url
causality
Suspect Entity
url
instance
value: MedicationAdministration/medication-administration-tucatinib
url
causality
Expected In Research Study: true
Adverse Event resolution date: 2021-01-21
Mitigating Action
url
item
modifierExtension[http://hl7.org/fhir/uv/ae-research-backport-ig/StructureDefinition/status]
actuality: actual
event: Nausea (Medical Dictionary for Regulatory Activities#10028813)
subject: Patient/patient-example-kaitlyn-b " BOUNCE"
date: 2020-05-25
seriousness: Non-serious (AdverseEventSeriousness#non-serious)
outcome: Not recovering/not resolved (NCI Thesaurus#C49494)
recorder: Practitioner/practitioner-oncology-nurse-jane " NURSE"