South San Francisco, CA — November 23, 2020 — Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY), today announced that the…
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FDA issues EUA to baricitinib plus remdesivir for COVID-19
(HealthDay)—Emergency use authorization was issued for baricitinib in combination with remdesivir for hospitalized patients with COVID-19, the U.S. Food and Drug Administration announced Thursday. The…
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Dog food recalled over salmonella concerns, FDA says
Fox News Flash top headlines for November 16 Fox News Flash top headlines are here. Check out what’s clicking on Foxnews.com. Heads up, dog owners:…
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FDA Approves Sklice (ivermectin) Lotion for Nonprescription Use to Treat Head Lice
October 27, 2020 — Today, the U.S. Food and Drug Administration approved a lotion to treat head lice for nonprescription, or over-the-counter (OTC), use through…
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FDA faults quality control at Lilly plant making Trump-touted COVID drug
Markets confident in stimulus, potential vaccine: Strategist Wells Fargo senior global markets strategist Scott Wren on his outlook for the markets. U.S. drug inspectors uncovered…
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Gilead’s Magrolimab, an Investigational Anti-CD47 Monoclonal Antibody, Receives FDA Breakthrough Therapy Designation for Treatment of Myelodysplastic Syndrome
FOSTER CITY, Calif.–(BUSINESS WIRE)–Sep. 15, 2020– Gilead Sciences, Inc. (Nasdaq: GILD) today announced that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Therapy designation for magrolimab, a…
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The FDA may approve a COVID-19 vaccine before trials are complete. Here’s what you need to know
With six million active cases and more than 180,000 deaths arising from COVID-19, as well as historic 32.9 percent economic contraction (via NPR), it’s no…
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US FDA revokes emergency use status of drug touted by Trump for COVID-19
Fox Business Flash top headlines for June 15 Fox Business Flash top headlines are here. Check out what’s clicking on FoxBusiness.com. The U.S. Food and…
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FDA issues safety alert for COVID-19 risk with fecal transplant
(HealthDay)—The U.S. Food and Drug Administration issued a MedWatch Safety Alert on Tuesday about the potential risk for SARS-CoV-2 transmission with the use of fecal…
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FDA Approves Trijardy XR
FDA Approves Trijardy XR (empagliflozin/linagliptin/metformin) for Type 2 Diabetes in Adults RIDGEFIELD, Conn., and INDIANAPOLIS, Jan. 27, 2020 /PRNewswire/ — The U.S. Food and Drug…
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