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3 dni temu · Key Takeaways. The FDA issued a recall notice for more than 7,000 bottles of duloxetine, a drug used to treat depression, anxiety, and nerve pain. The recalled lot may contain high levels of nitrosamines, a carcinogenic compound. The recall is Class II, meaning the health harms associated with taking the tainted medication are likely temporary ...
25 paź 2024 · 2 min read. Oct. 25, 2024 – Thousands of bottles of the medicine duloxetine are being recalled because they may contain a potentially cancer-causing agent. Duloxetine is the generic equivalent ...
25 paź 2024 · The voluntary recall was initiated earlier this month by the US Food and Drug Administration. Duloxetine, according to the Cleveland Clinic , treats depression, anxiety, fibromyalgia and chronic pain.
The Food and Drug Administration announced a Class II recall for more than 7,000 bottles of an antidepressant due to a chemical. The recall was initiated earlier this month on Oct. 10. Duloxetine ...
23 paź 2024 · The recall involves 7,101 bottles of duloxetine delayed-release capsules distributed nationwide within the United States, according to the FDA. The recalled capsules are 20mg in strength, and sold ...
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