Experts flag safety risks linked to Neurocrine’s Prader-Willi drug
Foundation for Prader-Willi Research and the International Prader-Willi Syndrome Organisation warned that serious adverse events, including edema and respiratory and cardiac complications, have been reported since Neurocrine’s Vykat XR became more widely available. They urged transparency despite saying reports do not prove a causal link. FDA’s AEMS shows seven death-linked reports as of July 31 and is evaluating whether regulatory action is needed.