**Cymbalta Recall: Toxic Chemical In Thousands Of Bottles**

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Post on Oct 24, 2024

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Cymbalta Recall: Toxic Chemical Found in Thousands of Bottles

A recent recall of Cymbalta capsules has sent shockwaves through the medical community and patient populations alike. The drug, a popular antidepressant used to treat a range of conditions including anxiety and chronic pain, has been found to contain a toxic chemical in thousands of bottles. This discovery has raised serious concerns about potential health risks and underscores the importance of carefully checking medications for any signs of contamination.

What is Cymbalta?

Cymbalta (duloxetine) is a serotonin and norepinephrine reuptake inhibitor (SNRI). It works by increasing the levels of serotonin and norepinephrine in the brain, which are neurotransmitters that regulate mood, sleep, appetite, and other important bodily functions.

Cymbalta is prescribed for a variety of conditions including:

• Major depressive disorder
• Generalized anxiety disorder
• Fibromyalgia
• Chronic musculoskeletal pain
• Diabetic peripheral neuropathy

The Recall and the Toxic Chemical

The recall was initiated by the manufacturer, Eli Lilly and Company, after discovering that **certain lots of Cymbalta capsules contained a chemical called N-nitrosodimethylamine (NDMA). NDMA is a probable human carcinogen that can be found in various environmental sources, including food, water, and air. Exposure to high levels of NDMA can potentially lead to liver cancer.

The recall affects specific batches of Cymbalta capsules, and the manufacturer has provided a list of affected lot numbers on their website.

It's important to note that:

• The presence of NDMA was not detected in all batches of Cymbalta.
• The level of NDMA found in the recalled batches is below the acceptable daily intake (ADI) set by regulatory authorities.

What Should You Do?

If you are taking Cymbalta:

1. Check your medication: If you have a bottle of Cymbalta, carefully check the lot number against the list provided by the manufacturer.
2. Contact your doctor: If your medication is part of the recall, contact your doctor immediately. They can advise you on the next steps, including whether to continue taking the medication, switch to a different medication, or take alternative measures.
3. Do not stop taking your medication suddenly: Stopping Cymbalta abruptly can have serious side effects. Always consult your doctor before making any changes to your medication regimen.

If you have taken Cymbalta and are concerned about potential health risks:

1. Consult your doctor: They can assess your individual situation and recommend appropriate monitoring or follow-up care.
2. Stay informed: Keep an eye on the news and official announcements regarding the recall for updates and information.

Takeaways

This Cymbalta recall serves as a stark reminder of the importance of medication safety and the need for vigilance regarding potential contamination. It also highlights the crucial role of open communication between patients, healthcare providers, and pharmaceutical companies in ensuring the well-being of individuals taking medication.

By staying informed and taking proactive measures, we can work together to mitigate the risks associated with medication recalls and ensure access to safe and effective treatments.