Washington: Despite experts raising doubts over the plasma therapy to treat Covid-19, the US Food and Drug Administration (FDA) has issued an emergency use authorisation (EUA) for convalescent plasma to treat …
US FDA approves blood plasma therapy to treat Covid-19 Read More Washington: The US Food and Drug Administration (FDA) has issued the first emergency use authorization (EUA) to Quest Diagnostics that allows COVID-19 pool testing for up to four individuals. Sample pooling …
US FDA issues 1st EUA for COVID-19 pool testing Read More
Washington: The White House has urged the US Food and Drug Administration (FDA) to reinstate its emergency use authorization (EUA) for the anti-malaria drug, hydroxychloroquine (HCQ), for COVID-19 treatment. Weeks ago, …
WH urges FDA to reconsider HCQ for COVID-19 treatment Read More Washington: The US Food and Drug Administration (FDA) has issued an emergency use authorization (EUA) for a COVID-19 antigen diagnostic test, the Becton Dickinson Veritor System for Rapid Detection of SARS-CoV-2. …
FDA issues emergency use authorization for COVID-19 antigen diagnostic test Read More
New York: The US is partially stopping the use of hydroxychloroquine (HCQ), which President Donald Trump personally obtained from India, and chloroquine (CQ) to treat COVID-19, suspending it in hospital settings …
US partially ends HCQ, CQ use for COVID-19 Read More Washington: At a time when hydroxychloroquine (HCQ) is being touted as a ‘wonder drug’ to treat critical Covid-19 patients, the US Food and Drug Administration (FDA) on Friday issued fresh guidelines, …
US FDA warns against popping over-the-counter HCQ pills Read More
San Francisco: Twitter has deleted a tweet posted by US President Donald Trump’s personal lawyer Rudy Giuliani and Republican activist Charlie Kirk for violating its rules over novel coronavirus misinformation. Giuliani …
Twitter deletes tweet by Trump’s attorney for corona misinformation Read More
Glenmark Pharmaceuticals Inc.,US (Glenmark) has been granted final approval by the United States Food & Drug Administration (US FDA) for Telmisartan and Hydrochlorothiazide. Tablets USP, a generic version of Micardis …
US FDA approves Glenmark’s generic version of Micardis HCT Tablets Read More
