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.
FDA duloxetine recall 2024: More than 7,000 bottles recalled
2 hours ago · 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 ...
Cymbalta, Duloxetine, recalled for containing cancer-causing …
7 hours ago · Towa issued the recall for 7,107 bottles, which covers 500-count bottles of 20mg Duloxetine Delayed-Release Capsules, Lot number: 220128, Exp. Date 12/2024, according to the Oct. 11 Class II ...
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 ...
Recall: prescription antidepressants recalled over potentially …
3 hours ago · NEW YORK (WPIX) – A pharmaceutical company issued a recall this month for thousands of bottles of duloxetine, a medicine often prescribed to treat depression. Over 7,100 bottles of duloxetine ...
7,100 bottles of antidepressant recalled by FDA now in 2nd
1 day ago · According to the FDA, Duloxetine -- which is marketed as Cymbalta -- is used to treat depression, anxiety, and other mood disorders. The drug is classed as a “selective serotonin/norepinephrine ...
Antidepressant recall: FDA upgrades medication risk class to 2nd ...
2 days ago · Duloxetine is used to treat depression, anxiety and nerve pain caused by fibromyalgia. However, low levels of a cancer-causing chemical called N-nitroso-duloxetine have been discovered during ...
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 FDA ...
Antidepressant recall: FDA upgrades risk level due to cancer
1 day ago · The drug treats depression, anxiety and nerve pain caused by fibromyalgia. ... News; Antidepressant recall: FDA upgrades risk level due to cancer-causing chemical ... Duloxetine is used to treat ...