FDA

U.S. regulators are delaying their decision on Moderna's COVID-19 vaccine for 12- to 17-year-olds while investigating the rare risk of heart infection, the company said on Sunday. The U.S. Food and Drug Administration told…

A panel of the US Food and Drug Administration advocated booster vaccination of Johnson & Johnson's one-time COVID-19 vaccine for people 18 years and older on Friday.J&J has asked the FDA for flexibility, arguing that the extra…

The Food and Drug Administration is grappling with whether and when to offer another dose of the one-off Johnson & Johnson COVID-19 vaccine, while a new study on Wednesday raises the prospect that using another brand as…

For the first time, the Food and Drug Administration approved an electronic cigarette on Tuesday, saying RJ Reynolds' vaping device can help smokers cut down on conventional cigarettes. E-cigarettes have been sold in the…

WASHINGTON (AP) - Drug maker Merck on Monday asked U.S. regulators to approve its pill against COVID-19, which would add an entirely new and easy-to-use weapon to the global arsenal against the pandemic.If it were approved by the Food…

People at significant risk of developing severe COVID-19, including millions of Americans with compromised immune systems, now have the option to receive preventive treatment with monoclonal antibodies if they have been…

A month after a controversial new Alzheimer's drug was approved, U.S. health officials signed new prescribing instructions Thursday that are likely to restrict its use. The Food and Drug Administration said the change is…