The U.S. Food and Drug Administration (FDA) has been forced to recall thousands of bottles of the antidepressant medication ...

The U.S. Food and Drug Administration has recalled thousands of bottles of the antidepressant Duloxetine for potentially cancer-causing chemicals in the medication.

For diabetic peripheral neuropathic pain, the recommended dosage is 60 mg per day, although dosages of up to 120 mg daily have been studied. [25] Higher dosages do not have proven benefit and may ...

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

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 ...

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 ...

The U.S. Food and Drug Administration has recalled thousands of bottles of the antidepressant duloxetine over the presence of a toxic chemical. According to an Oct. 10 notice from the agency ...

NEW YORK — Thousands of bottles of the antidepressant duloxetine, which is sold under the brand name Cymbalta, have been recalled due to the presence of a toxic chemical, according to a notice ...

Purpose: The pharmacology, pharmacokinetics, efficacy, safety, drug interactions, dosage and administration, cost, and place in therapy of duloxetine for major depression, pain from diabetic ...