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 for bresentrik

Page standards status: Informative

Generated Narrative: MedicationRequest

Resource MedicationRequest "medicationrequest-for-bresentrik"

identifier: http://www.bmc.nl/portal/medstatements/1234568900-studyDrug (use: official)

status: active

intent: order

medication: Medication/bresentrik: bresentrik 2mg tablet

subject: Patient/JanetPatient: Janet " CLINICAL TRIAL PATIENT"

supportingInformation: ResearchStudy/BreastCancerTrial

authoredOn: 2023-04-05

requester: : Could be reference to inline contained profile such as Reference(practitioner-1) Ronald Bone, MD

reasonCode: Breast Cancer (SNOMED CT#254837009)

instantiatesCanonical: http://baseUrlOfHospitalHolding/PlanDefinition/protocol-for-the-ResearchStudy

dosageInstruction

sequence: 1

text: 6 mg PO daily for remission induction; adjust dosage to white blood cell (WBC) count. With hold treatment if WBC is less than 15,000/µL; resume when WBC is greater than 50,000/µL

timing: Once per 1 days

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

doseAndRate

dispenseRequest

numberOfRepeatsAllowed: 1

quantity: 600 mg (Details: UCUM code mg = 'mg')

ExpectedSupplyDurations

-ValueUnitSystemCode
*30daysUnified Code for Units of Measure (UCUM)d