Some women on here may be using Cymbalta for neuropathy.
“More than 370,000 bottles of duloxetine delayed-release capsules, sold by New Jersey-based Breckenridge Pharmaceuticals and commonly known as Cymbalta, were subject to the warning.
The FDA raised the alarm after tests found the capsules contained higher than permitted levels of N-nitroso-duloxetine, which is considered to be a probable carcinogen to humans.“
I spoke to my pharmacist and she said since my brand was from a different manufacturer I am not affected by the recall. So please contact your pharmacist regarding the recall to see if your medication is on the list.
Is there a Cymbalta (duloxetine) recall that breast cancer patients using it for neuropathy should know about?
This is a really important thing to flag for the community. While the search results available don't contain specific details about a current Cymbalta recall, here's what to do right away:
- Check the FDA's Show Full Answer
The recall affects multiple batches of duloxetine delayed-release capsules, with specific lots identified as Lot 241069C and Lot 241180C, which are set to expire on May 31, 2027
I heard about the recall I am trying to get an answer I am still taking it myself. I will let you know once I find out.
If you decide to discontinue Duloxetine use, cold turkey is not recommended (withdrawal symptoms can be very severe).