FDA recalls shrimp sold at Walmart
Digest more
The Food and Drug Administration has authorized emergency use of animal drugs to treat and prevent infestations of the New World Screwworm, which poses an emerging threat to U.S. livestock and food security.
4h
The Well News on MSNFDA Cleared to Use Animal Drugs to Combat New World Screwworm Threat
WASHINGTON - The Food and Drug Administration was authorized Tuesday to use "animal drugs" on an emergency basis to treat and prevent infestations of the New World screwworm, a flesh-eating parasite that poses a threat to the U.
A series of panels convened by the Food and Drug Administration is raising concerns that the agency is skirting federal rules and promoting fringe views about antidepressants and other products.
The Food and Drug Administration (FDA) became authorized Tuesday to allow the use of animal drugs to treat or prevent infestations caused by the New World screwworm, a flesh-eating parasite that has recently disrupted the cattle industry.
The U.S. Food and Drug Administration has denied approval for PTC Therapeutics' oral medication for a rare genetic disorder with limited treatment options, the company said on Tuesday.
The Food and Drug Administration approved the weight loss drug Wegovy to treat an increasingly prevalent liver disease on Friday. Roughly 15 million people — six percent of adults in the United States — have metabolic dysfunction-associated steatohepatitis, known as MASH. Rates of the disease are rising.
The U.S. Food and Drug Administration reportedly secretly allowed substandard foreign factories to ship hundreds of medications to the U.S.
Lead is toxic to people of any age or health status and higher exposure levels can lead to neurological changes
Following decades of limited treatment options, people living with fibromyalgia will soon have access to a novel therapy designed to tackle the condition’s most elusive symptom: Poor-quality sleep. The US Food and Drug Administration (FDA) has just approved Tonmya,
The FDA urged consumers not to use the foam-style products because they may not be effective in protecting the skin from the sun's harmful UV rays.
When Hurricane Helene barreled across several southern states last fall, it destroyed homes and killed more than 150 people. The storm also took out one of the country’s main factories producing intravenous fluid bags widely used in hospitals.
Bristol Myers Squibb and SystImmune have announced breakthrough therapy designation from the US Food and Drug Administration (FDA)