The Federal Trade Commission on Friday filed lawsuits against three prescription drug benefit managers or PBMs over concerns ...
The function is not a diagnostic tool, but can tell watch-wearers if they are exhibiting signs of sleep apnea.
The FDA and manufacturers routinely allow doctors and hospitals to continue using medical devices that could cause serious ...
The U.S. Food and Drug Administration has declined to approve Vanda Pharmaceuticals' drug to treat stomach paralysis symptoms ...
Reuters.com is your online source for the latest news stories and current events, ensuring our readers up to date with any ...
For CNM-Au8, Clene has more than 700 patient-years of safety data that show no significant safety concerns or safety trends identified. No serious adverse events (SAEs) have been identified as related ...
Unlike rival CDK 4/6 inhibitor abemaciclib, patients don't need to be lymph-node positive to receive ribociclib after surgery ...
Like clockwork, Apple hosts its iPhone launch event every September. Here's what the company unveiled during its annual Apple ...
Children ages 12 and older with sickle cell are now eligible for a newly FDA-approved treatment through the MACC Fund Center ...
The National Service Scheme (NSS) unit of the National Institute of Technology (NIT), Kurukshetra, organised an event to ...
MIPLYFFA is the first FDA-approved treatment for Niemann-Pick disease type C (NPC), an ultra-rare and progressive ...
The FDA in 2020 asked manufacturers to pull the drug off the market ... Jim Hood formerly headed Associated Press Broadcast News, directing coverage of major news events worldwide. He also served as ...