News

Sarepta Therapeutics is pausing shipments of its gene therapy for muscular dystrophy following several patient deaths that ...
The FDA's assessment of the bread recall has designated it as a Class II risk, which means the product "may cause temporary ...
A Food and Drug Administration expert panel has reignited a debate over whether hormone therapy should be used to treat ...
This latest approval builds on an earlier liquid formulation of generic methimazole for feline hyperthyroidism, which ...
Taking medication for an allergic reaction? You might face severely itchy skin as a side effect of Zyrtec or Xyzal, according ...
Dr. George Tidmarsh, a Stanford pediatrics adjunct professor and former pharmaceutical executive, is FDA Commissioner Marty Makary’s pick to be the nation’s top drug regulator.
Packaged food makers in the U.S. have rolled out plans to eliminate the use of FD&C colors - a category of synthetic dyes - ...
Lexi Homberger — a third grade teacher at Dodge Elementary — was recognized in 2023, by the Williamsville School Board, after ...
The Food and Drug Administration has identified a Class I recall of certain lots of Medline Industries Craniotomy ...
This is the web edition of D.C. Diagnosis, STAT's twice-weekly newsletter about the politics and policy of health and ...
For decades, Coke and other beverage makers have used high fructose corn syrup or artificial sweeteners in their U.S. sodas.
The FDA granted an orphan drug designation to novel hedgehog pathway inhibitor taladegib, also known as ENV-101, for treating ...