Adverse Event Clinical Research R4 Backport
1.0.1 - STU1
Adverse Event Clinical Research R4 Backport
1.0.1 - STU1
This page is part of the Adverse Event Clinical Research R4 Backport (v1.0.1: STU 1) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version. For a full list of available versions, see the Directory of published versions
| Page standards status: Informative |
Generated Narrative: MedicationAdministration
Resource MedicationAdministration "medication-administration-tucatinib"
status: completed
medication: tucatinib 150 MG Oral Tablet (RxNorm#2361290)
subject: Patient/patient-example-kaitlyn-b " BOUNCE"
effective: 2020-04-01
| Actor |
| Practitioner/practitioner-oncology-nurse-jane " NURSE" |
request: MedicationRequest/medication-request-example-tucatinib
note: Patient took 2 tablets (By Practitioner/practitioner-oncology-nurse-jane @2020-04-01)
| Route | Dose |
| Oral route (qualifier value) (SNOMED CT#26643006) | 300 MG (Details: UCUM code MG = 'MG') |
IG © 2020+ HL7 International / Biomedical Research and Regulation. Package hl7.fhir.uv.ae-research-backport-ig#1.0.1 based on FHIR 4.0.1. Generated 2024-04-30
Links: Table of Contents |
QA Report
| Version History |
|
Propose a change