The Food and Drug Administration said Wednesday it is wrestling with whether and when recipients of the single-shot Johnson &
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FDA approves Roche drug for non-small cell lung cancer
The U.S. Food and Drug Administration has approved Roche’s Tecentriq as adjuvant treatment following surgery and platinum-based chemotherapy, for adults
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augmentin copii
Fox News Flash top headlines for October 5 Fox News Flash top headlines are here. Check out what’s clicking on
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CDC, FDA recommend Pfizer booster shot for 65 and up, people at high risk, health care workers
Following the recommendations of its vaccine advisory committee, the Food and Drug Administration gave emergency use authorization to Pfizer-BioNTech’s COVID-19
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FDA official hopeful younger kids can get shots this year
The Food and Drug Administration’s vaccine chief said Friday the agency will rapidly evaluate COVID-19 vaccinations for younger children as
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U.S. FDA to review use of GBT's blood disorder therapy in children
(Reuters) – Global Blood Therapeutics Inc said on Tuesday the U.S. Food and Drug Administration had granted priority review for
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arthritis medicine from ireland
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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FDA Approves Expanded Botox (onabotulinumtoxinA) Label to Include Eight New Muscles to Treat Adults with Upper Limb Spasticity
NORTH CHICAGO, Ill., July 29, 2021 /PRNewswire/ — Allergan, an AbbVie (NYSE: ABBV) company, today announced that the U.S. Food
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FDA Approves Keytruda (pembrolizumab) Plus Lenvima (lenvatinib) Combination for Patients With Certain Types of Advanced Endometrial Carcinoma
KENILWORTH & WOODCLIFF, N.J.–(BUSINESS WIRE) July 22, 2021 — Merck (NYSE: MRK), known as MSD outside the United States and
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FDA Approves Soaanz
FDA Approves Soaanz (torsemide) for Edema Treatment in Patients with Heart Failure and Renal Disease VIENNA, VA. (PRWEB) JUNE 21,
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