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The Food and Drug Administration authorizes the Pfizer–BioNTech COVID-19 vaccine for children between the ages of 5 and 11, becoming the first vaccine to be approved for children in the United States.
2021-10-29

The Food and Drug Administration gives full approval to the Pfizer–BioNTech COVID-19 vaccine, becoming the first vaccine in the U.S. to be granted full licensure and thereby giving businesses, schools and universities more confidence to adopt vaccine mandates.
2021-08-23

The U.S. Food and Drug Administration says that it has granted priority review for the vaccine developed by Pfizer and BioNTech. A decision on whether to fully approve the vaccine will likely be made within two months.
2021-07-16

The Food and Drug Administration approves the single-dose Johnson & Johnson vaccine for emergency use in the United States.
2021-02-27

The United States Food and Drug Administration (FDA) lifts the 32-year-old, lifetime ban on blood donations from gay and bisexual men. Men can donate if they haven't had sex with another man in the previous year. The FDA stance is in line with other countries, such as Australia, Brazil, Canada, New Zealand, and the U.K., and is consistent with rules on recent blood transfusion or accidental exposure to another individual's blood.
2015-12-21

The United States Food and Drug Administration approves the Merck & Co. drug, Bridion, that reverses the effects of muscle relaxants used during surgery.
2015-12-15

The United States Food and Drug Administration approves marketing of a cooling cap system to reduce hair loss in female breast cancer patients during chemotherapy. The DigniCap scalp cooling system, a product first available in Sweden in the 1990s, produces near-freezing temperatures that make it harder for cancer-fighting drugs to reach and harm hair follicles. [https:--www.usnews.com-news-politics-articles-2015-12-08-fda-clears-cold-cap-to-save-hair-during-breast-cancer-chemo (AP via U.S. News and World Report)] [http:--www.fda.gov-NewsEvents-Newsroom-PressAnnouncements-ucm476216.htm (FDA)] [http:--www.dignicap.com-dignitana-fda-clearance- (DigniCap)]date=August 2019
2015-12-8

The United States Food and Drug Administration names Taylor Farms as the source of cyclospora parasite tainted salads that sickened 223 diners in the US states of Nebraska and Iowa.
2013-08-2

The United States Food and Drug Administration approves the use of the drug Belimumab (Benlysta) to treat lupus, the first drug to be approved for this purpose in 56 years.
2011-03-9

Surgeons at the Shepherd Center in Atlanta, Georgia inject a spinal cord injury patient with embryonic stem cells in an experiment approved by United States Food and Drug Administration.
2010-10-11