FDA Announces Cymbalta Recall: Important Information

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Post on Oct 24, 2024

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FDA Announces Cymbalta Recall: Important Information You Need to Know

The U.S. Food and Drug Administration (FDA) has announced a voluntary recall of certain lots of Cymbalta (duloxetine) capsules due to the potential presence of a foreign substance. This recall is a serious matter, and it's essential for anyone taking Cymbalta to understand the risks involved and what actions to take.

What is Cymbalta?

Cymbalta is a prescription medication used to treat major depressive disorder (MDD), generalized anxiety disorder (GAD), fibromyalgia, and chronic musculoskeletal pain. It is a serotonin-norepinephrine reuptake inhibitor (SNRI), meaning it works by increasing levels of serotonin and norepinephrine in the brain.

What is the Recall About?

The FDA has issued this recall due to the potential presence of metal particles in some lots of Cymbalta capsules. These particles could be sharp and pose a serious health risk if ingested.

Which Lots of Cymbalta Are Recalled?

The recall affects specific lots of Cymbalta 20 mg and 60 mg capsules. The following information is crucial:

• Manufacturer: Eli Lilly and Company
• Drug: Cymbalta (duloxetine) capsules
• Affected Lots:
  • 20 mg capsules: Lots 00008474, 00008475, 00008476, and 00008477
  • 60 mg capsules: Lots 00008518, 00008519, 00008520, and 00008521
• Expiration Dates: February 2024

What Should I Do If I Have Recalled Cymbalta?

If you have any of the recalled lots of Cymbalta, immediately stop taking the medication and contact your healthcare provider. Your doctor will advise you on the next steps, which may include:

• Getting a replacement prescription: Your doctor may prescribe a different lot of Cymbalta or an alternative medication.
• Returning the recalled medication: You may be instructed to return the recalled medication to your pharmacist or to dispose of it safely according to your local regulations.

It is essential to follow your doctor's instructions carefully.

Symptoms of Metal Ingestion

If you suspect you have ingested metal particles from Cymbalta, seek immediate medical attention. Symptoms of metal ingestion can include:

• Abdominal pain
• Nausea and vomiting
• Diarrhea
• Bleeding

What to Do If You Have Any Concerns

If you have any questions or concerns about this recall, please contact your healthcare provider or the FDA directly. You can find more information about the recall on the FDA's website.

The FDA and Eli Lilly and Company are committed to ensuring the safety of patients. This recall is a reminder of the importance of being aware of potential medication risks and taking proactive steps to protect your health.