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US FDA expands GSK s RSV vaccine approval to adults aged 50 to 59

The U.S. Food and Drug Administration approved the expanded use of GSK s respiratory syncytial virus vaccine on Friday in adults aged between 50 and 59, making it the first shot endorsed for that age.

US FDA expands GSK s RSV vaccine approval to adults aged 50 to 59

US FDA expands GSK s RSV vaccine approval to adults aged 50 to 59
yahoo.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from yahoo.com Daily Mail and Mail on Sunday newspapers.

FDA advisers vote against first MDMA-based PTSD therapy

A U.S. Food and Drug Administration advisory panel on Tuesday voted against a therapy based on the party drug MDMA for patients with post-traumatic stress disorder, marking a setback to the nascent. -June 04, 2024 at 05:39 pm EDT - MarketScreener

FDA panel to review psychedelic drug MDMA for first time

By Sriparna Roy and Pratik Jain (Reuters) - A panel of advisers to the U.S. Food and Drug Administration will meet on Tuesday to discuss a therapy based on the psychedelic drug MDMA for patients with post-traumatic stress disorder (PTSD). The meet.

EU regulator recommends use of Pfizer s gene therapy for rare bleeding disorder

EU regulator recommends use of Pfizer s gene therapy for rare bleeding disorder
yahoo.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from yahoo.com Daily Mail and Mail on Sunday newspapers.

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