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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Cuba on Friday approved two more domestic COVID-19 vaccines for emergency use, the island nation’s medication regulatory body said. The
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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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Cuba on Friday approved its home-grown Abdala coronavirus vaccine for emergency use, the first developed in Latin America. The CECMED
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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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FDA Approves Brexafemme
FDA Approves Brexafemme (ibrexafungerp) as the First and Only Oral Non-Azole Treatment for Vaginal Yeast Infections JERSEY CITY, N.J., June
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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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Japan approves Moderna, AstraZeneca vaccines
Japan formally approved Moderna and AstraZeneca’s COVID-19 vaccines on Friday, but the latter will not be used immediately because of
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FDA Approves Jemperli
FDA Approves Jemperli (dostarlimab-gxly) for Women with Recurrent or Advanced dMMR Endometrial Cancer London UK 22 April 2021 — GlaxoSmithKline today
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