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  2. It should not be used in individuals with kidney or liver problems, congestive heart failure, or an allergic reaction to metformin. Some common side effects associated with Glucophage include nausea, diarrhea, and stomach upset, although these side effects are typically temporary and mild.

  3. Search list of recalled metformin products | FDA - U.S. Food and...

    www.fda.gov/drugs/drug-safety-and-availability/search-list-recalled-metformin...

    Find out which specific metformin products are affected by the recall. Linkedin. FDA Updates and Press Announcements on NDMA in Metformin. Show entries. Export Excel. Company. Medicine. NDC....

  4. Why the FDA Recalled Metformin Over a Cancer-Causing Agent

    www.verywellhealth.com/metformin-cancer-5116117

    Why Metformin Was Recalled. What You Should Do. In May 2020, the Food and Drug Administration (FDA) released a statement regarding higher-than-acceptable levels of a substance called N-nitrosodimethylamine (NDMA) in some preparations of extended-release metformin.

  5. FDA Updates and Press Announcements on NDMA in Metformin

    www.fda.gov/.../fda-updates-and-press-announcements-ndma-metformin

    Update [10/5/2020] FDA is alerting patients and health care professionals to two voluntary recalls of extended release (ER) metformin by Marksans Pharma and Sun Pharmaceutical Industries.

  6. Metformin Side Effects: Common and Severe - Healthline

    www.healthline.com/health/diabetes/metformin-side-effects

    In 2021, one brand recalled two lots of metformin extended-release tablets from the U.S. market, as reported by the Food and Drug Administration (FDA). This is because an unacceptable level of...

  7. Teva Pharmaceuticals USA, Inc. Initiates Voluntary Nationwide ...

    www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/teva...

    Teva Pharmaceuticals USA, Inc. Initiates Voluntary Nationwide Recall of Metformin Hydrochloride Extended-Release Tablets USP 500 mg and 750 mg Due to Detection of N-Nitrosodimethylamine (NDMA)...

  8. Metformin Recall: NDMA Contamination - Health

    www.health.com/condition/type-2-diabetes/metformin-recall

    Viona Pharmaceuticals Inc., issues voluntary nationwide recall of metformin HCl extended-release tablets, USP 750 mg, due to the detection of N-nitrosodimethylamine (NDMA) impurity.

  9. Metformin Recall Type 2 Diabetes Drug Recalled By the FDA - ...

    www.healthcentral.com/condition/type-2-diabetes/metformin-recall

    178 lots of metformin hydrochloride, the most common type 2 diabetes drug, were recalled in 2020 by the FDA.

  10. Diabetes Drug Recalled Due to Risk of Cancer - AARP

    www.aarp.org/health/conditions-treatments/info-2022/metformin-recall-cancer...

    Viona Pharmaceuticals has voluntarily recalled 33 batches of its Metformin Hydrochloride Extended-Release 750 mg tablets sold in 100-count bottles with expiration dates ranging from June 2022 to March 2023, the Food and Drug Administration (FDA) announced on Dec. 28.

  11. Type of Metformin Being Recalled - Prevention

    www.prevention.com/.../viona-metformin-extended-release-recall-carcinogen

    Viona Pharmaceuticals, Inc. is voluntarily recalling 23 lots of Metformin Hydrochloride Extended-Release Tablets due to the presence of the probable carcinogen NDMA. The pharmaceutical company...