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.
The Supreme Court said Monday it will leave in place an Oklahoma court ruling that struck down a state law limiting drug-induced abortions.
An experimental hepatitis C drug from Johnson & Johnson has won unanimous support from government advisers who say the medication should be approved to treat patients infected with the liver-destroying virus.