BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Information letter regarding Anemet® 200 mg tablets (dolasetron): Discontinuation of production

Active substance: dolasetron

Due to the risk of arrhythmias in connection with the administration of Anemet® 200 mg tablets to adults for prevention and treatment of nausea and vomiting associated with cytostatic chemotherapy, the pharmaceutical manufacturer has renounced this indication as a precautionary measure on its own responsibility. Production will be discontinued.

Download DHPC / Information letter , Download_VeroeffentlichtAm_EN PDF, 143KB, File is accessible