The U.S. Food and Drug Administration has recalled over 7,000 bottles of the antidepressant duloxetine, which is commonly sold under the name Cymbalta. According to the FDA, the drug was recalled ...

Cymbalta (duloxetine) can cause a range of side effects when you stop taking it, especially if you discontinue it abruptly.

According to an Oct. 10 notice from the agency, the recall involves 7,107 bottles of duloxetine, which is sold under the brand name Cymbalta. Duloxetine is part of a class of drugs called ...

Information about nitrosamine impurities in medications. National Library of Medicine: DailyMed. Cymbalta—duloxetine hydrochloride capsule, delayed release [drug label].

The U.S. Food and Drug Administration announced a Class II recall for more than 7,100 bottles of Duloxetine — a generic antidepressant for Cymbalta — due to a cancerous chemical. A voluntary ...

South Africans using duloxetine or Cymbalta can consult their pharmacists to discuss any concerns, particularly regarding nitrosamine exposure, and explore safe alternatives if needed. The drug is ...

Cymbalta is the brand name for duloxetine, and Effexor XR contains the active drug venlafaxine. These are prescription drugs ...

Over 7,100 bottles of Duloxetine were voluntarily recalled by the medication's company beginning Oct. 10 Alamy Duloxetine packaging The U.S. Food and Drug Administration has recalled thousands of ...