A Duloxetine recall by the FDA has flagged more than 7,100 bottles of the Cymbalta generic drug due to a cancerous chemical.
The Duloxetine Delayed-Release Capsules' voluntary recall began on Oct. 10 after the FDA deemed the medication the ...
The U.S. Food and Drug Administration has recalled thousands of bottles of the antidepressant duloxetine over the presence of ...
The recall was initiated due to the discovery of N-nitroso-duloxetine, a chemical impurity classified as a nitrosamine.
The FDA has recalled thousands of bottles of the antidepressant duloxetine, sold under brand name Cymbalta, due to the ...
The Food and Drug Administration (FDA) has recalled over 7,000 bottles of the popular antidepressant duloxetine – sold under ...
Thousands of bottles of a popular antidepressant medication are being recalled due to the presence of what the National ...
Thousands of bottles of a popular antidepressant medication are being recalled due to the presence of what the National Library of Medicine describes as a toxic chemical, according to a notice from ...
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FDA Recalls 7,000 Bottles Of Possibly Carcinogenic AntidepressantThe Food and Drug Administration (FDA) has issued a Class II recall for over 7,000 bottles of duloxetine, a popular ...
The FDA's recall involves 7,107 bottles containing 500 delayed-release 20 milligram duloxetine capsules, which are prescribed to treat conditions such as anxiety, depression, nerve pain related to ...
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Over 7,100 bottles of prescription antidepressants recalled over potentially cancer-causing substanceaccording to a recall notice. They were prescribed in 20mg delayed-release capsules, in 500-count bottles. Duloxetine may ...
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