In June, the Food and Drug Administration (FDA) expanded approval to all DMD patients aged 4 and older. DMD is a severe type of muscular dystrophy that leads to rapid muscle weakness; patients often ...

Herbals LLC has issued a nationwide recall of all lots of Vail-Bon Jie Yang Wan  supplement capsules due to the presence of ...

The spray was distributed by Green Pharmaceuticals Inc., of Camarillo, Calif., and had been sold on the company’s website and ...

Zevra Therapeutics has won Food and Drug Administration approval of Miplyffa for Niemann-Pick disease type C, making it the first drug cleared in the U.S. for the rare neurodegenerative disorder.

The products are being advertised as more affordable alternatives to blockbuster weight-loss drugs. Here’s what doctors think about them.

Beyond MariTide, Amgen has a rich pipeline with more than 30 phase 3 programs. Some are for existing medicines seeking label expansions, such as Lumakras and Amjevita, a rheumatoid arthritis medicine.

Listen up parents! There's a major recall you need to know about concerning a particular brand of baby powder. According to ...

Dynarex Corp. is recalling 62 cases of its Dynacare Baby Powder after sample testing revealed that the finished product contained asbestos, a known carcinogen.

(Reuters) - The U.S. Food and Drug Administration approved Zevra Therapeutics' drug for a rare and fatal genetic disorder, ...

Mammogram providers are now federally required to tell their patients about their breast density. The new U.S. Food and Drug Administration standards for ...

The Food and Drug Administration announced the recall of 62 cases of baby powder that could be contaminated with asbestos.

With Chevron overturned, physicians may not feel immediate effects – but behavioral health practices could face consequences.