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21mon MSN
The study, published Monday in the journal Pediatrics, found a 763% increase in the rate of reported nicotine pouch ...
The FDA expanded the indication for finerenone (Kerendia) in heart failure (HF), drug manufacturer Bayer announced.
Agriculture Secretary Brooke Rollins and Health and Human Services Secretary Robert F. Kennedy Jr. will hold a news briefing ...
2h
Stars Insider on MSNFDA issues alert, recall for contaminated blueberriesOn July 1, the FDA upgraded its recall of Alma Pak organic blueberries to Class I—the highest alert—after Listeria ...
British drugmaker GSK said on Monday it had submitted an application to the U.S. Food and Drug Administration to extend the ...
The U.S. Food and Drug Administration approved a new blue color additive derived from the fruit of the gardenia, a flowering evergreen, for use in a variety of drinks and candies.
The FDA evaluates glofitamab and daratumumab for lymphoma and myeloma treatments, highlighting trial demographics and ...
Kerendia was originally approved in July 2021 to reduce cardiovascular and kidney complications in patients with chronic ...
FDA Commissioner Marty Makary's vision for the agency risks the best of an agency that mostly has functioned well for the ...
The manufacturing-related rejection for UX111 is more than a setback for Ultragenyx, as it also delays a key test of the new ...
Capricor Therapeutics's dip caused by the CRL is a buying opportunity considering the readout of HOPE-3 within 2-3 months.
Finerenone gained FDA approval for heart failure treatment, showcasing significant benefits in reducing cardiovascular events ...
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