A drugmaker working to develop a pill to boost sexual desire in women says regulators are demanding more studies on the experimental drug.
The Food and Drug Administration says there’s no reason to believe that the coloring added to sodas is unsafe. But the agency is taking another look just to make sure.
The Food and Drug Administration on Friday cleared a first-of-a-kind blood test that can help diagnose mental disabilities in babies by analyzing their genetic code.
A new warning issued by the U.S. Food and Drug Administration urges Americans to be cautious when using over-the-counter laxatives.
The Virginia dietary supplement maker central to a gift scandal involving Gov. Bob McDonnell is illegally marketing two products.
On Monday, officials with the Food and Drug Administration proposed a rule that would require manufacturers of antibacterial hand soaps to prove that their products are safe to use on a daily basis over an extended period of time.
The co-owner of a now-defunct Virginia drug company has pleaded guilty to illegally importing Botox and other prescription drugs and selling them to physicians in violation of the Food and Drug Administration’s regulatory scheme.
Wednesday the FDA warned that heart attacks may be triggered by two specific injectable drugs, Lexiscan and Adenoscan, which are both manufactured by Astellas Pharma US. The side effect is rare, but is serious.
The Food and Drug Administration is seeking a rule change to allow generic drugmakers to quickly update their warning labels with new safety information for doctors and patients.
The Federal Food and Drug Administration is looking to drop trans fat in processed foods citing health concerns over heart attacks and deaths.