HL7 FHIR Implementation Guide: Common Terminology Criteria (CTC) Adverse Events Release 1 - DRAFT
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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

Example AdverseEvent: ctc-adverse-event-anemia1-persona-2

Generated Narrative: AdverseEvent

Resource AdverseEvent "ctc-adverse-event-anemia1-persona-2"

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: 2020-12-21

actuality: actual

event: Hgb 9.0 per CBC results from 12/21/20 (MedDRA Am Engl[20.0]#10002272 "Anemia")

subject: Patient/PatientPersona2 " C."

encounter: Encounter/encounter-ae1-evaluation-persona2

recorder: Practitioner/us-core-practitioner-nancy-oncology-nurse " NURSE"

suspectEntity

instance: MedicationAdministration/medadmin-doxorubicin-persona-2

Causalities

-ProductRelatedness
*probable

study: ResearchStudy/clinical-trial-example-soc