The Food and Drug Administration and the National Institutes of Health are awarding millions in funding to create 14 centers to conduct research on tobacco products.
A biotech drug from Roche moved one step closer Thursday to becoming the first medicine approved to treat breast cancer before surgery.
On Wednesday, the U.S. Food and Drug Administration announced that they plan to implement labeling changes on prescription opioids for the sake of safety.
A Food and Drug Administration review concludes that menthol cigarettes likely pose a greater public health risk than regular cigarettes but does not make a recommendation on whether to limit or ban the minty smokes — one of the few growth sectors of the shrinking cigarette business.
The Food and Drug Administration has approved the first medical scan that can help diagnose attention deficit hyperactivity disorder in children by measuring brain waves.
The Food and Drug Administration on Thursday approved unrestricted sales of Plan B One-Step, lifting all age limits on the emergency contraceptive.
President Barack Obama’s administration can go forward with its new plan to make the morning-after pill available to buyers of any age without prescriptions, but it needs to do it promptly or face potential sanctions in the long-running dispute over access to the emergency contraceptives, a federal judge ruled Wednesday.
Federal health regulators say an experimental insomnia drug from Merck can help patients fall asleep, but it also carries worrisome side effects, including daytime drowsiness and suicidal thinking.
The government is running out of time to try to halt implementation of a federal judge’s ruling that would lift age restrictions for women and girls wanting to buy the morning-after pill.
President Barack Obama says he’s comfortable with his administration’s decision to allow over-the-counter purchases of a morning-after pill for anyone 15 and older.