enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. FDA recalls more than 233,000 bottles of antidepressant over ...

    www.aol.com/news/fda-recalls-more-233-000...

    More than 233,000 bottles of an antidepressant have been recalled by public health officials due to a chemical containing the risk of cancer.. The U.S. Food and Drug Administration classified ...

  3. FDA recalls over 7,000 bottles of antidepressant due to ... - AOL

    www.aol.com/fda-recalls-over-7-000-200319107.html

    The Food and Drug Administration has announced a recall for thousands of bottles of the antidepressant duloxetine, sold under brand names like Cymbalta, due to the presence of a chemical that can ...

  4. The Food and Drug Administration (FDA) issued a Class II recall of more than 7,100 bottles of the antidepressant duloxetine due to the possible presence of a carcinogen. Duloxetine belongs to a ...

  5. Drug recall - Wikipedia

    en.wikipedia.org/wiki/Drug_recall

    A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall. [1]

  6. List of withdrawn drugs - Wikipedia

    en.wikipedia.org/wiki/List_of_withdrawn_drugs

    Diversion, abuse, and a relatively high rate of overdose deaths in comparison to other drugs of its group. This drug continues to be available in most of the world including the US, but under strict controls. Terfenadine (Seldane, Triludan) 1997–1998 France, South Africa, Oman, others, US Prolonged QT interval; ventricular tachycardia [2] [3]

  7. Is there a 2024 Duloxetine recall? FDA flags 7,100+ bottles ...

    www.aol.com/2024-duloxetine-recall-fda-flags...

    The U.S. Food and Drug Administration announced a Class II recall for more than 7,100 bottles of Duloxetine — a generic antidepressant for Cymbalta — due to a cancerous chemical.. A voluntary ...

  8. FDA recall policies - Wikipedia

    en.wikipedia.org/wiki/FDA_recall_policies

    FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.

  9. FDA recalls more than 7,000 bottles of antidepressant over a ...

    www.aol.com/fda-recalls-more-7-000-154029555.html

    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 ...