**Thousands Of Cymbalta Bottles Recalled Due To Chemical**

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Post on Oct 24, 2024

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Thousands of Cymbalta Bottles Recalled Due to Chemical Contamination

A major recall has been issued for thousands of bottles of Cymbalta, the popular antidepressant, due to potential contamination with a chemical that could cause serious health risks. The recall, announced by the Food and Drug Administration (FDA), affects specific lots of the medication manufactured by Eli Lilly and Company.

What is Cymbalta?

Cymbalta (duloxetine) is a prescription medication used to treat a range of conditions including:

• Major Depressive Disorder (MDD)
• Generalized Anxiety Disorder (GAD)
• Chronic Musculoskeletal Pain
• Diabetic Peripheral Neuropathy

What is the Contaminating Chemical?

The chemical found in the recalled bottles is N-nitroso-duloxetine, a nitrosamine. Nitrosamines are a group of chemicals that are potentially carcinogenic, meaning they can increase the risk of cancer.

Which Lots are Recalled?

The FDA has identified specific lots of Cymbalta that are affected by the recall. These lots are identified by their lot number and expiration date. It is crucial to check your Cymbalta bottle to see if your lot number and expiration date match any of the recalled lots.

To find out if your specific lot number is included in the recall, you can:

• Visit the Eli Lilly and Company website.
• Contact Eli Lilly and Company directly.
• Contact your pharmacist.

What Should I Do if I Have a Recalled Bottle?

If you have a bottle of Cymbalta that is part of the recall, do not take it.

Here are the next steps you should take:

• Stop using the medication immediately.
• Contact your doctor or pharmacist to discuss alternative treatment options.
• Return the recalled bottles to your pharmacy or dispose of them properly according to your local regulations.

What are the Potential Health Risks?

The potential health risks associated with ingesting N-nitroso-duloxetine are still being investigated. However, it is important to note that nitrosamines are potentially carcinogenic.

If you have taken a recalled bottle of Cymbalta, it is essential to monitor your health closely and contact your doctor immediately if you experience any unusual symptoms.

What is Eli Lilly and Company Doing?

Eli Lilly and Company is cooperating fully with the FDA to investigate the cause of the contamination and to ensure the safety of all its products. The company has also issued a statement expressing its regret for any inconvenience caused by the recall.

Where Can I Find More Information?

For more information about the Cymbalta recall, you can visit the FDA website, the Eli Lilly and Company website, or contact your healthcare provider.

This recall highlights the importance of checking medication labels and staying informed about potential safety concerns. If you have any questions or concerns, please do not hesitate to contact your healthcare provider.