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";s:4:"text";s:4042:"The FDA warns to stop selling the recalled product since NDEA could cause cancer in humans. Only certain lots of valsartan made in India and China have been recalled. Lawyers see the prospect for thousands of suits after contaminants turned up in the widely prescribed drugs.Lawyers see the prospect for thousands of suits after contaminants turned up in the widely prescribed drugs.Dozens of lawsuits have been filed against drug makers and sellers over widely prescribed generic heart medications tainted with potential carcinogens, the first claims in what some lawyers expect to be a wave of litigation.Millions of Americans have taken the drugs, which are at the center of a widening recall being overseen by the U.S. Food and Drug Administration, and have been for decades used to treat high blood pressure, heart failure and other common conditions.A lawyer involved in an effort to combine about 50 lawsuits, including at least 27 by patients who say they contracted cancer by using the recalled medicine, told a U.S. federal court he expects a surge of legal action. Very helpful with any questions and concerns and I can't thank them enough for the experience I had. It is sometimes combined with other drugs like Amlodipine, which also treats high blood pressure. “My best estimate sitting here today is I expect that we will have approximately 2,000 personal-injury cases on file in the next two years,” Daniel Nigh, who has filed 12 such lawsuits so far, told judges at a conference in the U.S. District Court in New Jersey last month, according to a transcript.The FDA has been coordinating a recall of adulterated heart medications since last July, when the carcinogen NDMA was discovered in valsartan manufactured by Zhejiang Huahai Pharmaceutical Co. The FDA has estimated that for every 8,000 people who took the highest dose of valsartan, there would be one additional case of cancer. Almost 40 defendants have been sued so far.The FDA has said that the pills may have been contaminated with NDMA for as long as four years before the problem was found. It is sometimes combined with other drugs like Amlodipine, which also treats high blood pressure. You can cross-check your valsartan Additionally, contact your local pharmacist or the drug manufacturer for information about the proper disposal of recalled valsartan. As such, it can attract weaker cases that piggyback on strong ones, he said.“You can never tell with MDLs on the number of viable or strong cases as opposed to the weak ones,” Tobias said.The lawsuits are combined in In Re: Valsartan Products Liability Litigation, 19-md-02875, U.S. District Court, District of New Jersey (Camden)The Zhejiang Huahai Pharmaceutical headquarters and production complex stands in Linhai, China.“I expect that we will have approximately 2,000 personal-injury cases on file in the next two years.”Updates with details from multidistrict litigation hearing in 25th paragraph and corrects spelling of Judge Kugler’s name. The designation suggests use of the affected product is unlikely to cause adverse health consequences. ...Valsartan is a commonly-prescribed high blood pressure medication. The information covered by the order would come in addition to material that the defendants have already agreed to produce.MDLs can include thousands of claims, some of which would never pan out or even be brought if filed separately, said law professor Carl Tobias of the University of Richmond law school. It is also used to treat angina, which is chest pain that happens when there isn’t enough blood flowing to the heart. The FDA Alert(s) below may be specifically about amlodipine or relate to a group or class of drugs which include amlodipine. ...Valsartan is a commonly-prescribed high blood pressure medication. Shortly after it announced the start of the recall in July, the FDA estimated that for every 8,000 people who took the highest dose of valsartan, there would be one additional case of cancer. Brought to you by The Meneo Law Group, LLP. 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