Register of adverse reactions
Description
The register shall contribute to safe and effective use of medicinal products, by continuously and systematically recording, treating and analysing adverse events reports and intercepting adverse event information from drug use as early as possible.
Information recorded in the register may also be made available for the management, planning and quality improvement of medicinal products and drug use and for research.
Resources
| Name |
Format |
Description |
Link |
|
8 |
|
https://helsedata.no/no/soknadsveiledning/personidentifiserbare-opplysninger/ |
Tags
- bivirkningshendelse,-om-legemiddelbrukeren,-informasjon-om-legemiddelbruken,-legemiddel,-melder,-identifisering-av-melding