BfArM - Federal Institute for Drugs and Medical Devices

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European Database on Adverse Drug Reaction Reports

ADR-Reports

In the European database of suspected adverse drug reactions, you can view data on suspected adverse drug reactions, also known as adverse drug reactions (ADRs), for medicines approved in the European Economic Area (EEA). For centrally authorized medicines, access is granted by both the name of the medicine and the name of the active ingredient. For non-centrally authorized medicines, access is only granted via the name of the active ingredient.

European Database on Adverse Drug Reaction Reports

Reporting adverse reactions

Reporting risks

The joint database of BfArM and Paul-Ehrlich-Institut (PEI) offers the option of digital reporting of adverse drug reactions for healthcare professionals and patients.