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2nd oral antiviral for treatment of COVID-19, molnupiravir, receives FDA EUA

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NewsDesk  @infectiousdiseasenews The U.S. Food and Drug Administration issued an emergency use authorization (EUA) for Merck’s molnupiravir for the treatment of mild-to-moderate coronavirus disease...

FDA issues Emergency Use Authorization for the Janssen COVID-19 Vaccine, the 3rd to date

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On Saturday, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) for the third vaccine for the prevention of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory...

U.S. FDA authorizes Moderna mRNA vaccine against COVID-19 for emergency use

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By NewsDesk  @bactiman63 Cambridge, MA  biotechnology company pioneering messenger RNA (mRNA) therapeutics and vaccines, Moderna, Inc., announced Friday that the U.S. Food and Drug Administration’s...

AMA Statement on FDA Authorization of First COVID-19 Vaccine

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By NewsDesk  @bactiman63 In a statement Friday from Susan R. Bailey, M.D., President, American Medical Association (AMA), she says the following: “For much of this year, physicians, nurses and frontline...

FDA issues EUA for the Pfizer-BioNTech COVID-19 vaccine

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By NewsDesk  @bactiman63 On Friday, the U.S. Food and Drug Administration issued the first emergency use authorization (EUA) for a vaccine for the prevention of coronavirus disease 2019 (COVID-19) caused...

COVID-19 vaccines update: Outbreak News This Week, Episode 3

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In this news podcast, I look at the success and progress of the Pfizer and Moderna vaccines and their situation concerning receiving and Emergency Use Authorization (EUA). Today, the Centers for Disease...

COVID-19 testing: Hologic’s Panther Fusion SARS-COV-2 Assay, LabCorp’s RT-PCR test issued EUAs from FDA

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On Monday, the U.S. Food and Drug Administration took two additional significant diagnostic actions during the coronavirus outbreak (COVID-19) by issuing Emergency Use Authorizations (EUAs) to: Hologic...