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    Antidepressant Recall: FDA Investigates Risks of Cancer-Causing Chemical

    4 hours ago

    The recall of Duloxetine Delayed-Release Capsules due to elevated levels of a potentially cancer-causing chemical has sparked concerns across the U.S. This medication, commonly prescribed for depression, anxiety, and nerve pain, was found to contain N-nitroso-duloxetine above acceptable limits set by the FDA. Nitrosamines, the group of chemicals to which N-nitroso-duloxetine belongs, can pose health risks when consumed in higher concentrations over time.

    The FDA stressed that patients should not discontinue their medications without consulting healthcare professionals. The agency is actively investigating the source of these impurities and will provide updates to the public. This high-risk recall underscores the importance of medication safety and regulatory oversight in the pharmaceutical industry. Patients affected by the recall are advised to seek guidance from their healthcare providers about alternative treatment options. Stay informed for further developments on this issue. The recall of Duloxetine Delayed-Release Capsules highlights the critical need for rigorous quality control measures in the pharmaceutical industry to ensure patient safety. This incident serves as a stark reminder of the potential dangers posed by contaminants in medications, underscoring the importance of ongoing monitoring and prompt regulatory response to safeguard public health.

    Patients who rely on Duloxetine should prioritize open communication with their healthcare providers to determine the most suitable course of action. It is essential for individuals to stay informed and engaged in their healthcare decisions, especially in situations where medication safety is a concern. As regulatory authorities continue their investigation into this issue, it is crucial for patients to remain vigilant and proactive in seeking guidance to address any potential health risks associated with the recall.

    Source:

    https://www.newsweek.com/antidepressant-recall-health-fda-cancer-1971178


    Comments / 17
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    Beargirls @ Tahoe
    28m ago
    Don’t they properly test these pharmaceuticals thoroughly before putting them out on the market. WTF do we pay the EPA, CDER AND FDA FOR? AND THEY ARE JUST NOW FINDING OUT ABOUT THIS OR THEYVE KNOWN ALL ALONG? FILLING THEIR POCKETS AT THE EXPENSE OF THE LIVES OF THOSE TAKING THIS DRUG. OH, AND AT THE SAME TIME, HANDLING POPULATION CONTROL!!! 🤬🤬
    Kathymarie17
    56m ago
    I’ve been on this medication since it came out and at high doses. I’m wondering when the lawyers start calling for my class action lawsuit?
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