TGA finds undeclared semaglutide in counterfeit retatrutide after hospitalization

Тази статия се показва на английски, докато преводът ѝ не бъде обновен.

Australia's TGA reported a hospitalization after severe vomiting from a product sold as retatrutide caused a torn oesophagus. Laboratory testing found no retatrutide and instead detected undeclared semaglutide at approximately 8 times the level in registered semaglutide products. The alert concerns a counterfeit product, not retatrutide administered in a clinical trial. The TGA said retatrutide remains unapproved and warned against using unapproved peptide products.

Източник

  1. 01TGA tests counterfeit retatrutide product following serious adverse event report(отваря източника в нов раздел) Therapeutic Goods Administration

Засегнати пептиди

  1. В клинични изпитванияRetatrutideТроен агонист на GIP, GLP-1 и глюкагоновия рецептор39 Забранен от WADA
  2. ОдобренSemaglutideАгонист на GLP-1 рецептора31