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FDA Clears OTC Glucose Monitoring System for Weight Management

System integrates glucose biosensor with an AI-driven platform to show how food, activity, stress, sleep affect the body in ...
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FDA says it will publish reports of adverse events tied to drugs on daily basis

The FDA said it has begun publishing reports of adverse events concerning drugs on a daily basis, instead of quarterly, as it ...

FDA clears Papzimeos to treat adult respiratory papillomatosis

The Food and Drug Administration approved Papzimeos (zopapogene imadenovec-drba) for the treatment of adults with recurrent ...

FDA Announces Recall on Over 20,000 Cans of 7Up—Here’s What to Know

FDA recalls 7Up Zero Sugar Tropical Soda for being mislabeled full-sugar soda. The affected cans were sold in 12-packs in ...

People’s Pharmacy: Is there a way to petition the FDA to change a drug’s classification?

A. The Food and Drug Administration has approved montelukast to treat asthma, exercise-induced bronchoconstriction (trouble ...

Noodle Recall Update as FDA Issues Risk Warning

The FDA classifies this recall as Class II, which the agency describes as a situation "in which use of or exposure to a ...
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FDA starts 'real-time reporting of adverse event data' for first time

The U.S. Food and Drug Administration has started "real-time reporting of adverse event data," according to an annoucement ...

FDA approves new brain cancer treatment pill

FOX 13's Evyn Moon talked with health experts about a new breakthrough brain cancer treatment drug as the FDA has now ...

Outlook Therapeutics: Why The Odds Point To A Favorable FDA Decision

Outlook Therapeutics nears FDA decision on Lytenava, with EU sales, exclusivity, and high upside potential despite current ...