According to the FDA, the drug was recalled because it had the "presence" of N-nitroso-duloxetine, a nitrosamine, which is a chemical that could increase the risk of cancer. The recall was issued ...
The U.S. Food and Drug Administration is urging patients not to stop taking their prescribed medication if it falls under the ...
The FDA has recalled thousands of bottles of the antidepressant duloxetine, sold under brand name Cymbalta, due to the ...