Food and Drug Administration

With a third coronavirus vaccine now approved in the U.S., what is the difference between the vaccines and should you opt for one over the other?

Although the administration said children are not at immediate risk from current levels of toxic metals in baby food, it plans to bring the amount to as close to zero as possible. News4’s Susan Hogan has the details.

U.S. regulators have approved the first new drug in over a decade for children with ADHD, which causes inattention, hyperactivity and impulsivity

Johnson & Johnson says they have applied to the Food and Drug Administration for an emergency use authorization for its coronavirus vaccine.

U.S. regulators have approved the first long-acting drug combo for HIV, monthly shots that can replace daily pills.

The Food and Drug Administration issued emergency use authorization for the Moderna coronavirus vaccine on Friday night.

A Food and Drug Administration advisory panel voted 20-0 to recommend emergency use authorization for the Moderna coronavirus vaccine.

U.S. regulators have approved a genetically modified pig for food and medical products, but the company behind it says you won’t see it on supermarket shelves anytime soon.

The FDA announced on Tuesday that it has authorized the first coronavirus test that can be taken at home and without a prescription.

The Food and Drug Administration approved an emergency use authorization for Pfizer and BioNTech’s COVID-19 vaccine on Friday.

The FDA’s Dr. Peter Marks said Saturday that pregnant women should consult their doctor before taking the Pfizer vaccine, given that pregnant women were not part of the clinical trials for the emergency use authorization. “The provider and individual can make a decision about whether the benefits outweigh the risks,” said Marks. “[Taking the vaccine is] not something that we’re...

An advisory committee met Thursday and voted in favor of endorsing the Pfizer-BioNTech COVID-19 vaccine for emergency authorization, saying that the benefits outweigh the risks.

The first COVID-19 vaccines to be given in the U.S. are expected to get a green light from regulators under a process known as emergency use authorization.

U.S. health officials have allowed emergency use of the first antibody drug to help the immune system fight COVID-19.

U.S. regulators have approved the first drug for treating Ebola.

Fifteen adults have been poisoned after drinking hand sanitizer that contained methanol, the Centers for Disease Control and Prevention reported Wednesday. Methanol, or wood alcohol, is a toxic chemical that can lead to hospitalization or death if ingested. The Food and Drug Administration first warned of hand sanitizers with possible methanol contamination in June, citing nine products from Mexico. Since then, the list...

The Food and Drug Administration has issued recalls for 59 hand sanitizers that contain methanol, a toxic chemical that can be fatal if ingested.

The Food and Drug Administration says nine products produced by Mexico-based Eskbiochem SA de CV may contain methanol, which can be harmful if absorbed through the skin or ingested.

The U.S. Food and Drug Administration has for the first time approved a video game for treating attention deficit hyperactivity disorder in children

Federal health officials are warning about potential accuracy problems with a rapid test for COVID-19 made by Abbott Laboratories.