Aurobindo Pharma USA Recalls Blood Pressure Drug Due to Cancer Risk
Drug maker Aurobindo Pharma USA, Inc. has recalled 80 lots of Amlodipine Valsartan due to possible cancer risk. Valsartan is a drug used to treat high blood pressure and heart failure.
Information About the Valsartan Recall
According to the Food & Drug Administration (FDA), Aurobindo Pharma detected trace amounts of a carcinogen known as N-nitrosodiethylamine (NDEA) in Valsartan tablets.
The carcinogen NDEA can be found naturally in foods and the environment. But it is often added to gasoline and used as a stabilizer for industry materials.
Human carcinogens are substances that can harm cells and DNA, which could lead to cancer.
Aurobindo Pharma has voluntarily recalled Valsartan and there are no reports of illnesses related to the recall.
List of Affected Drugs
The recalls includes the following drugs:
- Amlodipine Valsartan Tablets USP (5mg/160mg, 10mg/160mg, 10mg/320mg, 5mg/320mg)
- Valsartan HCTZ Tablets USP (320mg/12.5mg, 320mg/25mg, 80mg/12.5mg, 160mg/25mg, 160mg/12.5mg, 320mg/25mg)
- Valsartan Tablets USP (320mg)
Possible Side-Effects of Valsartan
- Dizziness
- Lightheadedness
- Headache
- Flulike symptoms
- Diarrhea
Patients can report any side-effects to the FDA MedWatch.
Doctors have prescribed Valsartan to patients throughout the United States.
FDA Recommends Patients Continue Taking Valsartan
Patients should work with their doctor and pharmacist to find a replacement for Valsartan before stopping the drug.
Patients can contact Aurobindo Pharma USA, Inc by email or phone with any questions regarding the recall.
Contact an Experienced Drug Recall Attorney
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If you or a loved one have been injured by or have developed serious side-effects from the use of recalled medications or pharmaceuticals, contact Thomas J. Henry immediately. We represent clients/victims all over the country. We are available 24/7, nights and weekends.
