A warning from the U.S. Food and Drug Administration about dangerous counterfeit versions of Botox.
Health agencies are looking into unsafe Botox injections given at spas and elsewhere.
Uncomplicated urinary tract infections is a very common condition impacting women and the most frequent reason for antibiotic use, according to the FDA.
Inactive fragments of the bird flu virus that has sickened dairy herds in eight states have been detected in pasteurized milk, the Food and Drug Administration said Tuesday.
The FDA and U.S. Department of Agriculture (USDA) said in a press release that the viral remnants don’t pose a health risk to consumers.
Particles of bird flu were detected in some samples of pasteurized milk, though the virus in that form is not a threat to humans, the Food and Drug Administration (FDA) announced Tuesday. As a bird flu epidemic spreads through avian and cattle livestock across the country, the FDA increased testing of domestic milk supplies. Some
Inactive fragments of the bird flu virus that has sickened dairy herds in eight states have been detected in pasteurized milk, the Food and Drug Administration said Tuesday.
Inactive fragments of the bird flu virus that has sickened dairy herds in eight states have been detected in pasteurized milk, the Food and Drug Administration said Tuesday.
Inactive fragments of the bird flu virus that has sickened dairy herds in eight states have been detected in pasteurized milk, the Food and Drug Administration said Tuesday.
Two US health agencies are investigating and warning against counterfeit botox injections. Both the CDC and the FDA have begun investigating "counterfeit" or mishandled botox injections after multiple people in different states experienced harmful reactions to them.
The Food and Drug Administration on Monday approved a new treatment for a type of bladder cancer. The treatment, which will be sold under the brand name Anktiva, is intended for some patients suffering from certain types of non-muscle invasive bladder cancer, according to an FDA statement announcing the approval. News of the FDA action was first reported by Reuters, which said, "The therapy works by activating types of disease fighting white blood cells called natural killer (NK) cells and...
The recall comes years after surgeons say they first noticed problems with the HeartMate II and HeartMate 3, manufactured by Thoratec Corp., a subsidiary of Abbott Laboratories.