As pollen peaks for the season, the U.S. Food and Drug Administration is warning that some popular allergy medications could cause a rare but severe itching side effect.. The FDA said in a safety ...

Abbott’s first leadless pacemaker, the Aveir VR, was approved by the FDA in March 2022. Both of these products, however, only work in a single chamber of the heart.

U.K. study: HPV vaccine reduced cervical cancer rates by 87% in women who were vaccinated at 12 and 13 03:48. The maker of an at-home cervical cancer screening test said Friday it has won approval ...

At-home cervical cancer screening test gets FDA approval. How it works, availability The Teal Wand is an at-home vaginal sample self-collection device that tests for HPV.

Congresswomen press FDA on why a proposal to ban hair-straightening chemicals is delayed. Democratic Reps. Shontel Brown, Ayanna Pressley and Nydia Velazquez want to know why the FDA twice delayed ...

FDA moves to take prescription fluoride supplements off the market By . Brenda Goodman. Updated May 13, 2025, 2:36 PM ET. PUBLISHED May 13, 2025, 1:46 PM ET. Video Ad Feedback.

An FDA study found the blood test “can reliably predict” the presence of protein conditions associated with Alzheimer’s at the time of the test in cognitively impaired patients.

Experts warn about risks of new COVID-19 vaccine guidelines 04:32. The U.S. approved a new COVID-19 vaccine made by Moderna late Friday but with limits on who can use it — not a replacement for ...

The US Food and Drug Administration on Tuesday approved Hemgenix, a new drug to treat hemophilia. Manufacturer CSL Behring set the price at $3.5 million per treatment, making it the most expensive ...

The FDA said PFAS — once commonly found in a range of products, including pizza boxes, fast-food wrappers and microwave popcorn bags — are no longer used in food packaging.

FDA approves 1st COVID-19 test to be used at home. Lucira's COVID-19 All-In-One Test Kit is expected to cost $50 or less, according to the company website. Biba Adams. Nov 18, 2020.

Approval takes away the excuse that the vaccine's development was rushed and, thus, it is too dangerous. There's no longer any excuse.