UFIS-SWE-IG
0.1.0 - ci-build

UFIS-SWE-IG, published by UNICOM. This guide is not an authorized publication; it is the continuous build for version 0.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/joofio/ufis-swe-ig/ and changes regularly. See the Directory of published versions

Example RegulatedAuthorization: Altermol-500mg30mg-Tablet-SE-IS-RA

Generated Narrative: RegulatedAuthorization Altermol-500mg30mg-Tablet-SE-IS-RA

identifier: http://ema.europa.eu/fhir/marketingAuthorizationNumber/50802

subject: MedicinalProductDefinition: identifier = http://ema.europa.eu/fhir/mpId#SE-100001659-00050802,http://ema.europa.eu/fhir/eurdId#851; domain = Human use; status = Current; combinedPharmaceuticalDoseForm = Tablet; indication = Opiodkänslig smärta när enbart perifert verkande analgetika inte är tillräcklig. Kodein är indicerat för vuxna, ungdomar och barn äldre än 12 år för behandling av akut måttlig smärta, som inte anses kunna lindras av andra analgetika såsom paracetamol eller ibuprofen (enbart).; legalStatusOfSupply = Medicinal product subject to special medical prescription; classification = N02AJ06

type: Marketing Authorisation

region: Kingdom of Sweden

status: Valid

statusDate: 2015-11-12

holder: Organization Alternova A/S

Cases

-TypeDate[x]
*First Authorisation2015-11-12