(HealthDay)—Pfizer may soon seek U.S. Food and Drug Administration emergency authorization of its COVID-19 booster shot for anyone aged 18
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U.S. FDA recommends lower sodium in processed, packaged foods
FILE PHOTO: Signage is seen outside of the Food and Drug Administration (FDA) headquarters in White Oak, Maryland, U.S., August
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FDA greenlights COVID-19 booster vaccine for some immunocompromised patients
Fox News Flash top headlines for August 12 Fox News Flash top headlines are here. Check out what’s clicking on
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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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FDA Approves Lumakras
FDA Approves Lumakras (sotorasib) for KRAS G12C-Mutated Locally Advanced Or Metastatic Non-Small Cell Lung Cancer THOUSAND OAKS, Calif., May 28,
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FDA approves third COVID-19 antibody treatment for emergency use
A third antibody treatment designed to keep high-risk COVID-19 patients from being hospitalized was approved for emergency use by the
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Medtronic Recall of Heartware HVAD Equipment Is Class I, Says FDA
The US Food and Drug Administration has declared Medtronic’s recent recall of batteries, power, and data link cables and other
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Rapid COVID Tests Are Coming to Stores Near You
Editor’s note: Find the latest COVID-19 news and guidance in Medscape’s Coronavirus Resource Center. Scientists and lawmakers agree that
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FDA Clears Ponesimod (Ponvory), New Oral Drug for MS
The US Food and Drug Administration (FDA) has approved ponesimod (Ponvory), a new oral medication given once daily to treat
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Alzheimer’s Association Denies Conflict in Aducanumab Support
The Alzheimer’s Association is denying accusations by two researchers in the field and a watchdog group that its repeated endorsement
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