HL7 FHIR Implementation Guide: Common Terminology Criteria (CTC) Adverse Events Release 1 - DRAFT
0.0.1 - DRAFT
HL7 FHIR Implementation Guide: Common Terminology Criteria (CTC) Adverse Events Release 1 - DRAFT, published by HL7 International Clinical Interoperability Council. This guide is not an authorized publication; it is the continuous build for version 0.0.1 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/standardhealth/fsh-ae/ and changes regularly. See the Directory of published versions
Generated Narrative: AdverseEvent
Resource AdverseEvent "ctc-adverse-event-example-1"
Profile: CTC Adverse Event
CTC Adverse Event Grade: Moderate Adverse Event (CTCAE Grade Code System#2)
Adverse Event Expectation: Expected Adverse Event (NCI Thesaurus#C41333)
Adverse Event Resolved Date: 2020-05-21
Adverse Event Participant
url
function
value: authenticator (ParticipationType#AUTHEN)
url
actor
value: Practitioner/us-core-practitioner-owen-oncologist " ONCOLOGIST"
actuality: actual
event: DHN IV given (MedDRA Am Engl#10012174 "Dehydration")
subject: Patient/PatientPersona2 " C."
date: 2020-05-20
seriousness: Non-serious Adverse Event (NCI Thesaurus#C41336)
outcome: Resolved (AdverseEventOutcome#resolved)
recorder: Practitioner/PractitionerExample1 " ANYDOC"
suspectEntity
code: gefitinib 250 MG Oral Tablet (RxNorm#349472)
Causalities
Assessment Adverse Event Probably Related to Intervention (NCI Thesaurus#C53259)
Generated Narrative: Medication #medication-example-1
code: gefitinib 250 MG Oral Tablet (RxNorm#349472)