Thousands of bottles of a popular antidepressant medication are being recalled due to the presence of what the National ...
The U.S. Food and Drug Administration is urging patients not to stop taking their prescribed medication if it falls under the ...
The Food and Drug Administration issued a Class II recall of more than 7,100 bottles of the antidepressant duloxetine due to ...
A Duloxetine recall by the FDA has flagged more than 7,100 bottles of the Cymbalta generic drug due to a cancerous chemical.
Over 7,100 bottles of Duloxetine were voluntarily recalled by the medication's company beginning Oct. 10 The U.S. Food and ...
Duloxetine Delayed-Release Capsules were recalled because the pills may contain high levels of a cancer-causing chemical.
Some bottles of the antidepressant duloxetine, sold under the brand name Cymbalta, were recalled due to the presence of a ...
The FDA is recalling more than 7,000 bottles of the antidepressant duloxetine due to a possible cancer-causing chemical.
The U.S. Food and Drug Administration updated the risk level of a recalled antidepressant due to the product containing high ...
If you struggle with racing thoughts, rumination, or physical anxiety symptoms ... the only cannabis-derived medication to receive FDA approval. CBD’s analgesic, anti-inflammatory, and ...
More than a million people have been prescribed cannabis products in Australia, but many remain confused about the rules and ...
On October 11, the recall was classified as a class II recall by the FDA—a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health ...