Under the Federal Therapeutic Products Act (FPA), all health care providers are required to report serious and/or unknown or insufficiently mentioned adverse drug reactions in the Swiss drug monograph.
Pharmacovigilance in Switzerland consists of the National Pharmacovigilance Center of the Swiss Agency for Therapeutic Products Swissmedic, based in Bern, and 5 regional Pharmacovigilance Centers located throughout the country (Zurich, Basel, Geneva, Lausanne and Lugano). Under the national pharmacovigilance system, notifications of adverse drug reactions are sent by healthcare professionals and patients directly to Swissmedic or to individual Regional Pharmacovigilance Centers.
The reports will be processed and evaluated, then forwarded to the World Health Organization's International Center for Drug Safety.