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Formålet med prosjektet er å etablere en kilde til strukturert legemiddelinformasjon som understøtter behovene i sykehus. Informasjonen skal være elektronisk tilgjengelig gjennom et spørregrensesnitt til bruk i kliniske systemer.

Home Page: https://legemiddelverket.no/andre-temaer/fest/prosjektet-safest-gjennomforing

fhir idmp medications norway

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safest's Issues

Hvordan bør Data carrier identifier skille mellom NTIN og GTIN type produktkode?

Produktkodene som mottas fra farmalogg definerer en produktkodestandard, denne kan være NTIN eller GTIN.

På Identifier på pakning (MedicinalProductPackaged), bør man lage èn slice for hver type, med "fixed value" i system, altså:
dataCarrierIdentifierNTIN (system: https://farmalogg.no/produktkode/NTIN)
dataCarrierIdentifierGTIN (system: https://farmalogg.no/produktkode/GTIN)

Eller:
Lage èn slice, hvor system ikke er fixed value, og man legger riktig system inn, avhengig av typen produktkodestandard?

Referanse til SubstanceSpecification fra MedicinalProductIngredient sin Substance

I R5 (http://build.fhir.org/ingredient.html) ligger referanse til stoff som en "choice of type", man kan legge til enten en CodeableConcept eller en referanse til Substance/SubstanceDefinition.

Får man profilert inn liknende i R4? https://www.hl7.org/fhir/medicinalproductingredient.html

Code på Substance i MedicinalProductIngredient i R4 har kardinalitet 1-1, så denne kan ikke endres.
Forslaget som ligger på simplifier nå har en extension på denne, men jeg får ikke endret cardinaliteten på selve extension til å være maks 1. Jeg er ikke helt fornøyd med at man kan ha 0 til mange extensions med referanse til et stoff, det vil jo aldri være mer enn ett.

Se:
image

https://simplifier.net/safest/safest-medicinalproductingredient

Innspill?

National profile for submitting adverse event

There is interest from the regional health trusts to submit reports of adverse events from medical drugs, as well as the usage of vaccines. I am not sure if nutrimental supplements should be included as well.

The national portal Melde.no is established for submitting reports on medical errors and adverse outcomes. We are now looking into expanding this with an open API, with the intention of enabling system to system communication of adverse events from E*R source systems and/or electronic quality systems.

Our guess is that the resource AdverseEvent could be of interest.

Where could we find more information on the way forward for investigating this track?

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