Thousands of bottles of an antidepressant have been recalled by the U.S. Food and Drug Administration due to a cancerous ...
A Duloxetine recall by the FDA has flagged more than 7,100 bottles of the Cymbalta generic drug due to a cancerous chemical.
Some bottles of the antidepressant duloxetine, sold under the brand name Cymbalta, were recalled due to the presence of a ...
Thousands of bottles of a popular antidepressant medication are being recalled due to the presence of what the National ...
The FDA is recalling more than 7,000 bottles of the antidepressant duloxetine due to a possible cancer-causing chemical.
Researchers have uncovered numerous genetic variants that seem to play a role in people’s responses to painkillers and other ...
The Food and Drug Administration (FDA) issued a Class II recall of more than 7,100 bottles of the antidepressant duloxetine ...
The U.S. Food and Drug Administration is urging patients not to stop taking their prescribed medication if it falls under the ...
The U.S. Food and Drug Administration updated the risk level of a recalled antidepressant due to the product containing high ...
Over 7,100 bottles of Duloxetine were voluntarily recalled by the medication's company beginning Oct. 10 The U.S. Food and ...
Thousands of bottles of a commonly prescribed antidepressant drug were recalled because they contained a suspected cancer-causing chemical.
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 ...