Thousands of duloxetine bottles, an antidepressant sold as ... - CBS News
20 hours ago · The recall covers 7,107 bottles of duloxetine, the FDA said. The bottles include 500 delayed-release 20mg capsules. The lot number is 220128, with an expiration date of 12/2024.
Cymbalta, Duloxetine, recalled for containing cancer-causing …
7 hours ago · FDA continues to test and research possible sources for drugs found to contain nitrosamines.”. Towa issued the recall for 7,107 bottles, which covers 500-count bottles of 20mg Duloxetine Delayed ...
FDA Has Recalled Thousands of Bottles of Antidepressant Cymbalta
13 hours ago · Over 7,100 bottles of Duloxetine were voluntarily recalled by the medication's company beginning Oct. 10 Charna Flam is a writer-reporter at PEOPLE. She has been working at PEOPLE since 2023. Her ...
What to do if you’re taking antidepressants recalled by FDA
5 hours ago · 0:02. 0:57. The FDA is recalling thousands of bottles of duloxetine, the generic form of Cymbalta, due to high levels of a cancer-causing chemical found during manufacturing. The recall, announced ...
7,100 bottles of antidepressant recalled by FDA now in 2nd ... - mlive
1 day ago · Earlier this month the FDA announced a recall of 7,107 bottles of Duloxetine Delayed-Release Capsules because of an elevated level of a cancer-causing chemical known as N-nitroso-duloxetine.
Antidepressant recalled: 2nd-highest FDA risk level; drug
1 day ago · The FDA is assigning the drug duloxetine delayed-release capsules to the second-highest risk level after drug distribution company, Breckenridge Pharmaceutical Inc., voluntarily issued the recall ...
Antidepressant recall: FDA upgrades risk level due to cancer
1 day ago · The FDA is assigning the second-highest risk level to the recall of Duloxetine Delayed-Release Capsules, produced by Towa Pharmaceutical Europe, according to agency records and reported by SILive ...
Antidepressant recall: FDA upgrades medication risk class to 2nd ...
2 days ago · The U.S. Food and Drug Administration updated the risk level of an antidepressant recall to the second-highest level due to the product containing high levels of a cancer-causing chemical. Canva By
Nationwide antidepressant recall update as FDA sets risk class
5 days ago · The recall of the Duloxetine Delayed-Release Capsules, produced by Towa Pharmaceutical Europe, was initiated on October 10 and has been given the second highest risk classification by the...
Nationwide Antidepressant Recall Update as FDA Sets Risk Class …
The recall of the Duloxetine Delayed-Release Capsules, produced by Towa Pharmaceutical Europe, was initiated on Oct. 10 and has been given the second highest risk classification by the FDA. Duloxetine is a medication used to manage depression, anxiety, and …
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