An FDA database analysis shows that reported adverse skin events after GLP-1 receptor agonist use are rare but can include rash and pruritus, highlighting a need for further research, according to a ...
Metal‑fragment risk prompts WinCo to recall thousands of Margherita pizzas sold from California to Texas, FDA records show.
The agency plays a key role in tracking disease spread and vaccination rates. Last year, it seemed to back away from some of ...
An audit of U.S. Centers for Disease Control and Prevention (CDC) public databases found that nearly half of routinely ...
The FDA ImportShield Program centralizes import review, increasing processing speed by 66% and volume capacity by 33%, while ...
There has been an enduring controversy over whether psychiatric medications can trigger violent actions toward others. A review of the FDA's Adverse Event Reporting System by Thomas Moore, Joseph ...
Wrapped in a flashy fur coat she’d found at a thrift store for the occasion, Hannah Goetz blew out the candles on her favorite red velvet cheesecake. It was her 21st birthday. The celebration with her ...
The FDA said it plans to accept new forms of real-world evidence in product applications, starting with a subset of medical device submissions. The agency said the policy change aims to enable the use ...
Poherdy is the first interchangeable biosimilar to Perjeta, approved for HER2-positive breast cancer, expanding access to targeted therapies. Biosimilars like Poherdy meet rigorous FDA standards, ...
After the FDA rejected its spinocerebellar ataxia treatment, Biohaven missed out on a $150 million payment from Oberland Capital. Now the company is reshuffling its pipeline to stay alive. Biohaven is ...
Changsha Hospital of Traditional Chinese Medicine (Changsha Eighth Hospital), Changsha, China Background: No prior research has directly compared adverse drug event (ADE) profiles of Nivolumab and ...
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