lægemiddelregister

A lægemiddelregister, often translated as a drug register or medicine register, is a comprehensive database that collects and organizes information about medicinal products available in a particular country or region. These registers are typically maintained by national health authorities or regulatory bodies, such as the Danish Medicines Agency (Lægemiddelstyrelsen) in Denmark.

The primary purpose of a lægemiddelregister is to serve as an authoritative source of information for healthcare professionals, patients, and the public. It typically includes details such as the active ingredients, dosage forms, strengths, indications for use, contraindications, side effects, and prescribing information for each registered drug. This information is crucial for ensuring the safe and effective use of medicines.

Furthermore, lægemiddelregistre often contain data on the marketing authorization status of drugs, including when they were approved and by whom. They may also track prescription patterns, drug consumption, and pricing, which can be valuable for public health surveillance, economic analysis, and policy-making. Access to a lægemiddelregister can also facilitate pharmacovigilance efforts, allowing for the monitoring of adverse drug reactions and the identification of potential safety issues. In essence, a lægemiddelregister is a vital tool for transparency, safety, and informed decision-making within the healthcare system concerning pharmaceuticals.