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: Stesolid-10mg-Solution-SE-IS-RA

Generated Narrative: RegulatedAuthorization Stesolid-10mg-Solution-SE-IS-RA

identifier: http://ema.europa.eu/fhir/marketingAuthorizationNumber/9292

subject: MedicinalProductDefinition: identifier = http://ema.europa.eu/fhir/mpId#SE-100000064-00009292,http://ema.europa.eu/fhir/eurdId#1029; domain = Human use; status = Current; combinedPharmaceuticalDoseForm = Rectal solution; indication = Stesolid rektallösning är speciellt användbart vid manifesta kramper, som feberkramper, tetanus och eklampsi, vid status epilepticus samt för premedicinering och sedering. Stesolid rektallösning är indicerat också i andra akuta situationer då snabb, ångestdämpande eller sederande effekt önskas.; legalStatusOfSupply = Medicinal product subject to special medical prescription; classification = N05BA01

type: Marketing Authorisation

region: Kingdom of Sweden

status: Valid

statusDate: 1977-11-18

holder: Organization Actavis Group PTC ehf.

Cases

-TypeDate[x]
*First Authorisation1977-11-18