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2019.04.04
Active substance: Metamizol
The Federal Institute for Drugs and Medical Devices (BfArM) is implementing the corresponding implementation decision of the European Commission of 20 March 2019 in its decision of 28 March 2019.
The EMA recommends harmonizing the dosage of metamizole-containing drugs and their use during pregnancy and breastfeeding.
The European Medicines Agency (EMA) has started a review of medicines containing metamizole.
For details regarding the procedure please click on the following link to the European Medicines Agency (EMA):