Skip to main content

Plaintiffs To Submit Short-Form Complaint In Valsartan MDL

Plaintiffs To Submit Short-Form Complaint In Valsartan MDL

Plaintiffs To Submit Short-Form Complaint In Valsartan MDL

Introduction

On August 20, U.S. Magistrate Judge Joel Schneider made it mandatory for all Valsartan lawsuits to be filed along with a short-form complaint that will help in tracking and coordinating the cases. The order also requires the seven-page form to be completed by plaintiffs who have previously filed complaints within 30 days.

The short-form will help both parties and the court to divide the Valsartan cancer lawsuits more efficiently as the size of the MDL is expected to grow rapidly in the coming months, with an estimate of more than 2,000 lawsuits to be filed under the federal court system.

The short form complaint includes options of more than 50 manufacturers, distributors, repackagers, labelers, pharmacies, and wholesalers involved in the sale of contaminated valsartan pills, which impacted most of the U.S. supply for the hypertension drug in recent years. The form also provides a list of seven different kinds of cancers linked with injury the plaintiffs suffered including kidney, liver, colorectal, pancreatic, esophageal, stomach, and small intestine cancer.

Diovan (Valsartan) was manufactured by Novartis International AG and was approved by the FDA on August 14, 2002. Diovan lost its patent in September 2014. The launch of the generic drug had been on hold since patent expiry due to regulatory problems with the FDA. In 2014, a US-based Ohm Laboratories (Ohm), a subsidiary of Ranbaxy Laboratories, was the first to get the approval from FDA for generic Valsartan. Thereafter, many generic versions of Valsartan came into the market via many other pharma companies.

Currently, more than 100 lawsuits on Valsartan cancer cases are pending in the federal court system, each raising similar allegations that poor manufacturing techniques led to contamination of the pills with human carcinogens, which included N-nitrosodimethylamine (NDMA) and N-Nitrosodiethylamine (NDEA).

Since February 2019, Valsartan claims are consolidated under MDL No. 2875 (In re Valsartan Products Liability Litigation) in the United States District Court, District of New Jersey, presided by Judge Robert B. Kugler, U.S.D.J and Hon. Joel Schneider, U.S.M.J. 

Comments

Restricted HTML

  • Allowed HTML tags: <a href hreflang> <em> <strong> <cite> <blockquote cite> <code> <ul type> <ol start type> <li> <dl> <dt> <dd> <h2 id> <h3 id> <h4 id> <h5 id> <h6 id>
  • Lines and paragraphs break automatically.
  • Web page addresses and email addresses turn into links automatically.
CAPTCHA
Enter the characters shown in the image.
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.

Latest News

title demo for news

Categories: Settlements

created dropdown in quarterly-results page in localy, and explore all the component codes 

Zantac Settles 4,000 Lawsuits in U.S. Courts

Categories: General

Sanofi has announced a settlement agreement regarding approximately 4,000 Zantac cancer lawsuits filed in state courts across the country.

Valsartan Recall Lawsuit Set for Trial

Categories: General

Years after the initiation of Valsartan recalls, the U.S. District Judge overseeing lawsuits filed by individuals harmed by tainted versions of…

Our Legal Drafting Services    
start @ $25 per hour.