The U.S. Food and Drug Administration approved British drugmaker GSK's combination vaccine to protect against meningococcal ...
Explaining America’s weirdly complicated food inspection system, including who regulates poultry and eggs and how Robert F. Kennedy Jr. is involved ...
The U.S. Food and Drug Administration approved Merilog as biosimilar to Novolog for the improvement of glycemic control in adults and pediatric ...
Just a few weeks ago on January 15, the Food and Drug Administration (FDA) under the Biden administration revoked authorization of the additive red dye 3, meaning it will be banned from foods and ...
Welcome to the Philip Morris International fourth quarter 2024 and full year results conference call. [Operator instructions] ...
If you buy through a BGR link, we may earn an affiliate commission, helping support our expert product labs. For the first time in over two decades, the U.S. Food and Drug Administration (FDA) has ...
The Food and Drug Administration on Thursday approved a new type of nonopioid painkiller from Vertex Pharmaceuticals. The drug, Journavx, or suzetrigine, was approved to treat moderate to severe ...
When the U.S. Food and Drug Administration approves a prescription medication for adults, the drug is also approved for pregnant patients. But information about medication dosing during pregnancy ...
Robert F. Kennedy Jr., the anti-vaccine activist President Donald Trump has tapped to run the Department of Health and Human Services, recruited McAfee to apply for a job as the FDA's raw milk ...
FDA Milk Allergy Alert: Cal Yee Farms Chocolate Recall. Individuals with a milk allergy are being urged to exercise caution after the U.S. Food and Drug Administration (FDA) raised the alert level for ...
Shimla (Himachal Pradesh) [India], January 30 (ANI): Himachal Pradesh Police have busted an interstate gang involved in drug supply operations across multiple districts under Mission Clean. All of 17 ...
On Monday, the U.S. Food and Drug Administration classified the recall as "Class I," the most severe risk level. According to the FDA, "Class I" level recalls are used when there is "reasonable ...
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