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It’s important to report possible adverse events after medicine authorization. Consequently the benefit-risk ratio of the medicinal products can continuously be evaluated. Healthcare professionals are required to report all possible adverse events via the Federal Agency for Medicines and Health Products or via our contact page.


Belgium:
Federal Agency for Medicines and Health Products
Division Vigilance

EUROSTATION II

Victor Hortaplein, 40/ 40

B-1060 Brussels 

Website: www.fagg.be 

E-mail: adversedrugreactions@fagg-afmps.be 


Luxembourg :
Direction de la Santé
 

Division de la Pharmacie et des Médicaments 

Villa Louvigny – Allée Marconi 

L-2120 Luxembourg 

Website: http://www.ms.public.lu/fr/activites/pharmacie-medicament/index.html