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This report is prepared using the most recent information posted in the FDAs Enforcement Reports Database (for recalls), Warning Letters Database (for warning letters), and Drug Imports Alerts Database (for drug importers subject to import bans)
[3] [7] As of 2024, retatrutide has no UK marketing authorisation granted by the Medicines and Healthcare products Regulatory Agency (MHRA), and it has not received a marketing authorisation from the European Medicines Agency (EMA)
If any side effects you experience dont settle as you get used to the medication, let a physician know
Zealand Pharma is another important name because of licensing activity around survodutide
