The FDA has included more information about the risk of myocarditis on the label for the Pfizer and Moderna COVID-19 vaccines.

The FDA subsequently issued a Class I risk classification for the recall on July 8. Newsweek contacted Fuentes Farms LLC for comment by email outside of regular working hours.

The U.S. Food and Drug Administration (FDA) has added new warnings to the Pfizer and Moderna COVID-19 vaccines about a rare heart condition that mostly affects young men.

Dr. Marty Makary, the agency’s commissioner, said too many women avoid hormone therapy because the risks have been overstated ...

A recent cookie recall has escalated, with the U.S. Food and Drug Administration (FDA) now designating it as a Class I recall, which is the highest risk level. This move comes after New Grains ...

An agency-sponsored forum included critics of psychiatry who believe the drugs can harm a developing fetus. Other experts ...

An FDA-cleared predictive analytic tool for hemodynamic instability may soon leverage its success in critical care to the ...

The Class I recall status indicates that the product poses a risk of causing serious health consequences or death if consumed ...

The panelists said that vaginal creams and other localized therapies for menopause are safe and vastly underused by women who could benefit.

May 25, 2010 — The US Food and Drug Administration (FDA) today recommended that physicians exercise more caution in prescribing proton pump inhibitors (PPIs) in light of evidence suggesting that ...