The nationwide recall of more than 7000 bottles of duloxetine delayed-release capsules is due to unacceptable levels of a ...
A Duloxetine recall by the FDA has flagged more than 7,100 bottles of the Cymbalta generic drug due to a cancerous chemical.
The U.S. Food and Drug Administration has recalled thousands of bottles of the antidepressant Duloxetine for potentially ...
Some bottles of the antidepressant duloxetine, sold under the brand name Cymbalta, were recalled due to the presence of a ...
The U.S. Food and Drug Administration has recalled over 7,000 bottles of the antidepressant duloxetine, which is commonly ...
Over 7,000 bottles of the antidepressant medication duloxetine, sold under the brand name Cymbalta, have been recalled, the ...
The recall of the Duloxetine Delayed-Release Capsules, produced by Towa Pharmaceutical Europe, was initiated on October 10 ...
Thousands of bottles of an antidepressant have been recalled by the U.S. Food and Drug Administration due to a cancerous ...
The U.S. Food and Drug Administration updated the risk level of a recalled antidepressant due to the product containing high ...
The US Food and Drug Administration has recalled thousands of bottles of Duloxetine antidepressant, saying it contained high ...
Thousands of bottles of a commonly prescribed antidepressant drug were recalled because they contained a suspected cancer-causing chemical.
A voluntary recall was initiated on Oct. 10 by Breckenridge ... of nitrosamine drug substance impurity, N-nitroso-duloxetine. Per the FDA, nitrosamine impurities "may increase the risk of ...