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(Reuters) -The U.S. health regulator is delaying its decision on authorizing Moderna Inc’s COVID-19 vaccine for adolescents to check if
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FDA to authorize 3rd COVID-19 vaccine dose for immunocompromised people
On Thursday (Aug. 12), the U.S. Food and Drug Administration (FDA) is planning to authorize a third vaccine dose for
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Public trust in CDC, FDA, and Fauci holds steady, survey shows
With more than two-thirds of American adults vaccinated with at least one dose of an authorized COVID-19 vaccine, the top
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FDA Approves Kerendia
FDA Approves Kerendia (finerenone) for the Treatment of Patients with Chronic Kidney Disease Associated with Type 2 Diabetes WHIPPANY, N.J.–
Read moreFDA Approves Verkazia
FDA Approves Verkazia (cyclosporine ophthalmic emulsion) for the Treatment of Vernal Keratoconjunctivitis EMERYVILLE, Calif.–(BUSINESS WIRE) June 24, 2021 –Santen Inc.,
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BREAKING NEWS: FDA orders J&J to throw out 60M COVID-19 vaccine doses
BREAKING NEWS: FDA orders Johnson & Johnson to throw out 60 MILLION Covid vaccine doses made at Baltimore plant that
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FDA approves obesity drug that helped people cut weight 15%
Regulators on Friday said a new version of a popular diabetes medicine could be sold as a weight-loss drug in
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PRINCETON, N.J.–(BUSINESS WIRE) May 27, 2021 — Bristol Myers Squibb (NYSE:BMY) today announced that the U.S. Food and Drug Administration
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FDA Approves Myfembree
FDA Approves Myfembree as the First Once-Daily Treatment for Heavy Menstrual Bleeding Associated With Uterine Fibroids BASEL, Switzerland and NEW
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