Second COVID-19 vaccine nears FDA emergency authorization this week Fox News medical contributor Dr. Marty Makary discusses timetable for distribution
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Baricitinib and Remdesivir Combination Receives Emergency Use Authorization from the FDA for the Treatment of Hospitalized Patients with COVID-19
INDIANAPOLIS, Nov. 19, 2020 /PRNewswire/ — Eli Lilly and Company (NYSE: LLY) and Incyte (NASDAQ: INCY) announced today that the U.S. Food and Drug
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Pfizer will file for emergency FDA approval of covid vaccine TOMORROW
BREAKING NEWS: Pfizer will file for emergency FDA approval of its 95% effective vaccine TOMORROW – but Dr. Fauci warns
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Khondrion Receives Rare Pediatric Disease Designation for Sonlicromanol from US FDA
September 28, 2020 — Khondrion, a clinical-stage biopharmaceutical company discovering and developing therapies targeting mitochondrial disease, today announces that it
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Sophisticated modeling boosts split ventilators to emergency FDA review
, A new set of 3D-printed parts and an accompanying app is making ventilator splitters such as these much safer
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FDA warns of defective EpiPen dangers
(HealthDay)—Certain types of EpiPens and their generic counterparts may fail or delay injection of lifesaving epinephrine for severe allergic reactions,
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FDA approves coronavirus survivors' blood treatment in critical patients
Doctor with coronavirus: ‘If it can hit me, it can hit anybody’ Columbia University’s Center for Infection and Immunity director
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FDA issues tuna fish warning amid illness outbreak investigation
Fox News Flash top headlines for Nov. 18 Fox News Flash top headlines for Nov. 18 are here. Check out
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2011 FDA safety message tied to drop in transvaginal mesh use
(HealthDay)—A 2011 U.S. Food and Drug Administration safety communication correlated with a significant decline in transvaginal mesh use for treatment
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FDA reports more seizures among vapers
(HealthDay)—There have been 118 more reports of e-cigarette users suffering seizures since the U.S. Food and Drug Administration first warned
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