Valsartan Lawyer

Patients in American put a lot of faith and trust in their doctors and drug manufacturers. When a medication causes more problems than it solves, patients feel betrayed by the drug manufacturers they relied on to help them. If you are a Valsartan patient, you may have heard about the recalls that have been issued or you may have even received a letter from your pharmacy regarding the safety of this drug.

This can be a confusing time, although a Valsartan lawyer could help you pursue your legal rights if you have taken the recalled lots of this drug.

About Valsartan

Since 1996, Valsartan, an angiotensin receptor blocker (ARB), has been available by prescription to treat high blood pressure and congestive heart failure. It does have several known side effects for which there are warnings.

Up until 2018, this drug was believed to be relatively safe to use. Then investigators found that some lots of Valsartan contained N-nitrosodimethylamine (NDMA), a probable human carcinogen. These lots were isolated to these facilities:

  • Zhejiang Huahai Pharmaceuticals in China
  • Hetero Labs Limited, in India
  • Zhejiang Tianyu, in China

The FDA reports that NDMA was previously used to produce rocket fuel, antioxidants, additives for lubricants, and softeners for copolymers. If someone is exposed to NDMA over a long period of time they are at a higher risk for cancer of the kidneys, liver, pancreas, stomach, and intestine/colon/rectum. A Valsartan attorney could help those impacted exercise their legal rights.

Voluntary Recall of Valsartan for Patient Safety

In late 2018, the manufacturers of Valsartan and other related drugs issued a voluntary recall of their product. The manufacturers Teva Pharmaceuticals, Solco Healthcare, and Major Pharmaceuticals have all recalled their prescription drugs containing Valsartan. According to the FDA, the presence of NDMA in Valsartan was unexpected, and it is suspected to be related to changes in the manufacturing process.

A recall is a method of removing or correcting problems that are violating FDA laws. When a manufacturer finds out or has reason to believe that a medication is a risk, it is not only expected by the general public but also required by federal law that they will do the right thing by issuing a warning and recalling their product according to 21 CFR 7.

The actions on the part of the FDA came after more than 22 other countries issued Valsartan recalls. Understandably, patients in the United States who took Valsartan on a routine basis are now uncertain about their treatment. Many are consulting with their physicians for further advice as well as Valsartan legal counsel to weigh their legal options.

Drug Manufacturer Liability

Drug manufacturers have a responsibility to ensure the safety of the products they deliver to the public. When they fail to take the proper precautions, millions of people could be at risk worldwide. They are liable for any damages they cause when they deliver unsafe products.

Reach Out to a Valsartan Attorney Today

If you received a recall letter or know that you could have taken contaminated lots of Valsartan, it is time to reach out to an experienced Valsartan lawyer. With their help, you may be able to file a class-action lawsuit against the manufacturers of this drug with the goal of receiving compensation for your damages. Call today to receive your case consultation.