FDA

Two days before a panel of experts is set to review Moderna's COVID-19 vaccine and advise the Food and Drug Administration, documents show the vaccine is 94% effective and well-tolerated.

The Food and Drug Administration finds "no specific safety concerns" that would stand in the way of authorization of the vaccine for emergency use. Effectiveness is 95% after two doses.

The vaccine was found to be 95% effective in an updated study analysis. Safety data required by the Food and Drug Administration showed no serious concerns, the company said.

Central State University in Wilberforce has received a $1.3 million hemp research contract from the United States Food and Drug Administration.Central…

The Food and Drug Administration says it still needs more information from Columbus research firm Battelle about how it would respond to "adverse events"…

A Senate hearing on the coronavirus pandemic follows the day after the U.S. death toll from the coronavirus pandemic topped 200,000 people. The session is underway now.

The Food and Drug Administration's chief said Sunday the therapy reduces deaths among COVID-19 patients by 35%. On Monday he apologized, acknowledging that statistic greatly exaggerates any benefit.

Ali Schroer was just out of college when she started her first teaching job, but her new insurance plan didn’t cover her allergy medication. "So this...

Emergency use authorization makes it easier for doctors to use a drug in a manner not specifically approved by the Food and Drug Administration. The FDA granted these drugs this status in March.

Reproductive rights advocates want patients to be allowed to pick up mifepristone at a hospital or clinic. The drug, which was approved 20 years ago, also helps to manage miscarriages for some women.