Tag: European medicines agency

Since its establishment in 1995, the **European Medicines Agency (EMA)** has been responsible for the scientific evaluation and supervision of medicines across the European Union (EU) and European Economic Area (EEA). This vital regulatory body ensures that all human and veterinary medicines marketed within its jurisdiction meet stringent standards of quality, safety, and efficacy before they are made available to patients.

According to the European Medicines Agency (EMA), manufacturer Wyeth voluntarily withdrew its applications for Pristiq (desvenlafaxine) in Europe in 2008 after regulators expressed concerns over the drug's efficacy and risk-benefit profile. This was a withdrawal of applications for marketing authorization, not a ban, and it is the key reason **why did Europe ban Pristiq** is a misconception.