The U.S. Food and Drug Administration has approved Nucala (mepolizumab) as an add-on maintenance treatment for adult patients with inadequately controlled chronic obstructive ...

People who regularly use the allergy medications Zyrtec or Xyzal may experience severe itching when they stop, the U.S. Food ...

The supermarket chain Publix has recalled fruit and vegetable baby food sold in eight states because product testing found elevated levels of lead, according to federal health officials. Publix ...

But the FDA declared months ago that the shortages of semaglutide and tirzepatide injections had ended, effectively ending flexibilities for compounded products. The grace period for manufacturers to ...

Authorities say a security incident outside CIA headquarters has led to a shooting. Officers with the Fairfax County Police ...

U.S. senators questioned the head of the FDA today about who will be eligible for a COVID-19 booster in the fall. The agency now plans to restrict access to many Americans ...

Government advisers are meeting Thursday to decide if COVID-19 vaccines need updating to improve protection this fall and winter — even as a new Trump administration policy has ...

The Food and Drug Administration and the Centers for Disease Control are investigating a Salmonella outbreak linked to cucumbers.

FDA leaders say the agency will require more clinical trials to show the benefits of annual COVID shots for healthy adults.

After the the FDA declared an end to the shortage of GLP-1 medications, compounded versions of the drug must be out of the market by Thursday.

FDA changes COVID-19 vaccine approval policy, major trials now required for widespread use. Higher risk individuals still have access.