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 commonly prescribed antidepressant drug have been recalled by the FDA because they were found to ...
The Duloxetine Delayed-Release Capsules' voluntary recall began on Oct. 10 after the FDA deemed the medication the ...
The FDA recalled thousands of bottles of antidepressants after finding high levels of potentially cancer-causing chemicals. Here's what to look for.
The U.S. Food and Drug Administration (FDA) has issued a nationwide recall of thousands of bottles of antidepressants. These ...
Duloxetine Delayed-Release Capsules were recalled because the pills may contain high levels of a cancer-causing chemical.
The U.S. Food and Drug Administration updated the risk level of a recalled antidepressant due to the product containing high ...
Now, the FDA is assigning the second-highest risk level to the recall of Duloxetine Delayed-Release Capsules, produced by ...
The Federal Drug Administration issued a recall on Tuesday for a common medicine for depression. Over 7,000 bottles of ...
More than 7,100 bottles of Cymbalta is being pulled by the FDA after the toxic chemical was discovered. In addition to treat ...
The U.S. Food and Drug Administration is urging patients not to stop taking their prescribed medication if it falls under the ...
For MDD, duloxetine may be a useful alternative for patients who do not benefit from or are unable to tolerate other antidepressant therapy. Conclusion: Duloxetine has been approved for the ...