Adverse Event Clinical Research
1.0.1 - STU1 International flag

This page is part of the Adverse Event Clinical Research (v1.0.1: STU 1) based on FHIR (HL7® FHIR® Standard) v5.0.0. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions

MedicationRequest: Medication Request for discontinued clinical trial medication ABC

Page standards status: Informative

Generated Narrative: MedicationRequest

Resource MedicationRequest "medicationrequest-for-study-medication-administration-ABC"

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

status: stopped

intent: order

Medications

-Reference
*Medication/study-medication-ABC: study-medication-ABC 10 mg tablet

subject: Patient/SCHJO ""

supportingInformation: ResearchStudy/research-study-XYZ: http://baseUrlOfHospitalHolding/PlanDefinition/protocol-for-the-ResearchStudy

authoredOn: 2021-06-12

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

Reasons

-Concept
*Atrial fibrillation (SNOMED CT#49436004)

dosageInstruction

sequence: 1

text: 10 mg PO daily every morning

timing: Once per 1 days

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

doseAndRate

dispenseRequest

numberOfRepeatsAllowed: 1

quantity: 1000 mg (Details: UCUM code mg = 'mg')

ExpectedSupplyDurations

-ValueUnitSystemCode
*100daysUnified Code for Units of Measure (UCUM)d