BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Dear Doctor Letter (Rote-Hand-Brief) on ulipristal acetate (Esmya®): restricted indication, new contraindication and requirements for liver monitoring

Active substance: Ulipristalacetat

Treatment with Esmya may carry a risk of serious liver injury. After finalisation of the corresponding referral procedure, the following new measures to minimise the risk of serious liver injury will be implemented from now on: restriction of indication, new contraindication and requirements for liver function monitoring.

For details on the procedure please click on the following link to the homepage of the European Medicines Agency (EMA):

Risikobewertungsverfahren zum Arzneimittel Esmya®

Download DHPC / Information letter , Download_VeroeffentlichtAm_EN PDF, 430KB, File is accessible