The Food and Drug Administration announced Tuesday that it will relax a lifetime ban forbidding gay men to donate blood, if they have abstained from gay sex for one year.
The U.S. Food and Drug Administration released a study Tuesday that shows teens are using drugs less in the past years, but there has been a rise in using e cigarettes, International Business Times has reported.
On Monday, the U.S. Food and Drug Administration approved a new blood test that makes it easier for doctors to detect if someone is at risk for a heart attack and heart disease.
Dangerous substances found in government laboratories Deadly microbes were found in government labs from historical collections that were long-forgotten, but the National Institutes of Health said they have now been destroyed.
Consumer Reports is disputing recommendations from the U.S. Food and Drug Administration and the Environmental Protection Agency in regards to the amount of tuna pregnant women should consume.
On Monday, the U.S. Food and Drug Administration and the U.S. Environmental Protection Agency updated its draft advice for fish consumption, adding specific guidelines for women who are pregnant or breastfeeding.
On Saturday, Colorado Gov. John Hickenlooper signed a groundbreaking bill into law, which gives terminally ill patients access to experimental medicine not yet approved by the Food and Drug Administration.
A recent report released from the offices several U.S. lawmakers revealed several issues regarding the use of electronic cigarettes that include the lack of age restrictions and no uniform warning labels.
A growing number of doctors in the United States have been voicing an increased concern over the quality of generic medications imported from India, according to a recent in-depth report from Reuters. The concerns weighing on the minds of many doctors in the U.S. come from an increasing trend of recalls and import bans put in place recently by the Food & Drug Administration (FDA) on drugs made in India.
It'll be the first device available on the market to relieve pain caused by migraine headaches preceded by auras, the visual, sensory or motor disturbances experienced immediately before the onset of a migraine attack.
The U.S. FDA has approved the use of Allergan's Botox to lessen crow's feet. Meanwhile, in the UK, the MHRA approved Botox for the treatment of overactive bladder.
