NBC News' Berkeley Lovelace Jr. reports that some officials in the Food and Drug Administration are grappling with how to ...
The FDA has issued a Class I risk classification for a large number of recalled onions produced by Taylor Farms.
Revuforj was approved by the FDA for adults and children with relapsed/refractory acute leukemia with a KMT2A translocation.
The FDA’s REMS program has been found to have unintentionally created barriers to accessing clozapine, a crucial ...
Researchers, public health and health care groups, advocates, industry, and the public must put tackling diet-related disease ...
The US Food and Drug Administration (FDA) has approved Azurity Pharmaceuticals’ Danziten (nilotinib), the first and only ...
The FDA has warned providers of safety concerns and supply issues for Getinge/Maquet's VasoView HemoPro Endoscopic Vessel Harvesting Systems. The device is primarily used during endoscopic arterial ...
The FDA has approved revumenib (Revuforj) for the treatment of adult and pediatric patients aged 1 year and older with ...
The new rules, which cover both TV and radio, instruct drugmakers to use simple, consumer-friendly language when describing ...