The FDA approved the first drug in its class that targets moderate to severe acute pain in adults, without being addictive ...

Thus, the 3-day recall requires that respondents answer either three specific questions (for a once a day medication) or six specific questions (for a twice-a-day medication). A mistake of recall ...

Chief Medical Officer at Central DuPage Hospital Dr. Tom Moran joins Bob Sirott to talk about prostate cancer awareness and the FDA’s approval of a new pain medication. He also explains a study that ...

(CNN) — The US Food and Drug Administration signed off Thursday on the first new type of pain reliever to be approved in more than two decades. The drug, suzetrigine, is a 50-milligram ...

More Than 230,000 Bottles of a Popular Antidepressant Have Been Recalled ... a Pain & Fever Reducer Have Been Recalled Nationwide Nearly 8,000 Bottles of a Trusted Allergy Medicine Have Been Recalled ...

The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) has announced a major recall of DJ's Boudain sausages over concerns they may be contaminated with pieces of a pen.

Application of a multi-stacked fentanyl patch could result in serious, life-threatening, or fatal respiratory depression.

The U.S. Food and Drug Administration (FDA) approved Journavx (suzetrigine) oral tablets on Thursday as a first-in-class non-opioid analgesic to treat acute pain in adults. The new development is ...

(NEW YORK) — The U.S. Food and Drug Administration (FDA) on Thursday approved a new type of prescription pain medication for adults to treat moderate to severe acute pain. The drug, called ...

WASHINGTON (AP) — Federal officials on Thursday approved a new type of pain pill designed to eliminate the risks of addiction and overdose associated with opioid medications like Vicodin and OxyContin ...

Experts say the drug, which is billed as nonaddictive, could reduce the number of opioids patients are prescribed after surgery or be used by patients who can’t take other pain medications ...