Are you giving your pets food that's safe to eat? A new study may prove that there have been more than a few instances of pet food mislabeling. It turns out that out of 52 products, 20 were potentially mislabeled.
The U.S. Food and Drug Administration (FDA) has just approved a new immunotherapy drug to treat advanced melanoma that could prove to be a game-changer in fighting the health issue.
The Medicines and Healthcare Products Regulatory Agency (MHRA) of Britain was responsible for seizing millions of dollars in counterfeit medicine. Now, it turns out that the U.S. FDA made some busts as well in the international operation.
Prescription opioids have already been a salient issue in the medical world. Patients have misused the drugs for anxiety issues and recreational use. The FDA recently approved a new opioid analgesic, and many heath care, consumer and addiction drugs are concerned.
Researchers may have stumbled across a new tool to make colonoscopies less uncomfortable. At this time, inserting a long, thin and flexible tube into the colon is the only way to detect the possibility of ulcers, colon polyps, tumors or any areas of inflammation that could cause bleeding in the rect...
As of Monday, an advisory panel of medical experts voted to recommend the approval of a drug for both ulcerative colitis and Crohn's disease developed by Takeda Pharmaceutical Co.
The FDA has approved marketing of a new device that can be used to treat urinary symptoms related to enlarged prostate.
After added flak from the U.S. Food and Drug Administration for adding caffeine to candy, Wrigley is pulling their caffeine gum off the market. The FDA has also said that many of the energy foods are promoted with social media campaigns, which unfairly targets young people when too much caffeine can...
The Food and Drug Administration is taking an unusual step of reassessing the safety of the drug Avandia that is manufactured by GlaxoSmithKline
Following 45,000 reports of over the past seven years in lifesaving devices called automated external defibrillators, the U.S. Food and Drug Administration proposed on Friday to require all manufacturers to get agency approval.
There is new evident that a group of Type 2 diabetes drugs may increase patients risk of getting pancreatic cancer, the Food and Drug Administration (FDA) said Thursday, adding that they are looking into the research.
The US Food and Drug Administration (FDA) has approved Navidea Biopharmaceuticals Inc., Lymphoseek which is a radioactive imaging agent that checks if breast cancer or melanoma has spread to lymph nodes of a patient, the organization said in a statement released Thursday.