Adverse Event Clinical Research R4 Backport
1.0.1 - STU1 International flag

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

MedicationRequest: medication-request-example-tucatinib

Page standards status: Informative

Generated Narrative: MedicationRequest

Resource MedicationRequest "medication-request-example-tucatinib"

status: active

intent: order

medication: tucatinib 150 MG Oral Tablet (RxNorm#2361290)

subject: Patient/patient-example-kaitlyn-b " BOUNCE"

authoredOn: 2020-03-12

requester: Practitioner/practitioner-owen-oncologist " ONCOLOGIST"

dosageInstruction

text: oral twice a day every day

timing: Starting 2020-04-01, Once

route: Oral route (qualifier value) (SNOMED CT#26643006)

doseAndRate

maxDosePerAdministration: 2