Losartan, Irbesartan Cancer Lawsuits to be Consolidated with Valsartan Claims. Losartan is a popular blood pressure medication that has been voluntarily recalled multiple times due to the presence of a human carcinogen. Answering every question and concern I had throughout. In September 2019, ... Losartan Lawsuits. March 2019 — Camber Pharmaceuticals Inc. recalled 87 lots of Losartan because it may contain a cancer-causing impurity. Investigators found trace amounts of another carcinogenic impurity. Goldenberg Law “Losartan Recall Lawsuit”, Goldenberg Law. The FDA has announced a recall of hundreds of products containing Valsartan. The lawsuits stem from a July 2018 recall of several batches of valsartan that had been manufactured in China. However, it was not suitable as a drug, so scientists started looking into developing something more viable. It can also cause liver damage. Torrent Pharmaceuticals Limited is the manufacturer of the generic medication involved in the recall. The losartan recall expands again as Torrent Pharmaceuticals Limited issues another removal for its losartan potassium tablets USP and losartan potassium/hydrochlorothiazide tablets, USP. Losartan Potassium / Hydrochlorothiazide Tablets, USP 100mg/25mg, 90 count. The Valsartan Recall List. Losartan Recalls. Our law firm is filing lawsuits on behalf of individuals who took valsartan and have been diagnosed with liver damage, tumors, or cancer. Valsartan Recall Lawsuit . We are highly experienced losartan cancer attorneys who will answer your questions related to your irbesartan recall lawsuit, helping you navigate the issues associated with an amlodipine lawsuit. The impurity that has been detected is N-Methylnitrosobutyric acid or NMBA. 1. Alicia Proctor was a pleasure to work with. Losartan Lawsuit The FDA reported that they have found traces of unexpected impurities in certain batches of Losartan. However, any changes should be discussed at once and under a doctor’s supervision. This is the third blood pressure drug to have been recalled due to possible cancer risk. By 1995, the U.S. Food and Drug Administration had approved the drug for use in the United States. On March 25, 2019, Legacy Pharmaceutical Packaging issued a voluntary recall of 40 lots of Losartan potassium tablets due to NMBA. QUALITATIVE UND QUANTITATIVE ZUSAMMENSETZUNG Jede Filmtablette enthält 100 mg Losartan-Kalium, entsprechend 91,6 mg Losartan. The drugs were recalled because they were contaminated with the toxin N-nitrosodimethylamine, or NDMA. Search List of Recalled Angiotensin II Receptor Blockers (ARBs) including Valsartan, Losartan and Irbesartan. The FDA has a complete list of valsartan recalls on its website. The U.S. Food and Drug Administration (FDA) announced the initial recalls in 2018. They are amongst the most popular high blood pressure or Angiotensin receptor blocker (ARB) drugs available to consumers today. As a result, Losartan is one of the most popular drugs used to treat this condition and in … Free Confidential Lawsuit Evaluation: If you or a loved one has been diagnosed with cancer after taking Losartan, you should contact our law firm immediately. Losartan Wrongful Death Lawsuit Filed By Family of Woman Diagnosed With Liver Cancer (4/28/2020) Recalled Valsartan Pills Not Properly Preserved for Litigation, Plaintiffs Claim (1/21/2020) Joe Lyon is a highly-rated Cincinnati, Ohio product liability attorney and Losartan lawyer investigating Losartan recall lawsuits and cancer risks for plaintiffs nationwide. In a matter of mere months, the previously little-known pharmaceutical ingredient valsartan has gone from relative obscurity to being at the center of multiple drug recalls and at least one potential class-action lawsuit. This dangerous drug defect has led to a losartan recall announced by the U.S. Food and Drug Administration and can be the basis of a losartan cancer lawsuit by victims of the defective drug. A panel of federal judges has ruled that all lawsuits filed in U.S. District Courts across the country by plaintiffs who claim that they developed cancer from the generic blood pressure drugs losartan and irbesartan will be consolidated with the pending valsartan litigation. On Sept. 23, 2019 the Food and Drug Administration issued a voluntary nationwide recall of a popular and widely-prescribed blood pressure medication due to a cancer-related contamination. According to Cozaar’s official prescribing information sheet, clinical trials for Losartan have revealed common side effects that occur more frequently in those taking Cozaar versus those taking a placebo. We are highly experienced losartan cancer attorneys who will answer your questions related to your irbesartan recall lawsuit, helping you navigate the issues associated with an amlodipine lawsuit. Valsartan is a prescription drug used to treat hypertension and other various heart conditions. If a federal judge agrees to add losartan and irbesartan to the consolidated lawsuit, the effort could significantly expand the litigation against drug makers, distributors and sellers. The recalls deal with only certain types of drugs called angiotensin II receptor blockers (ARBs), and more specifically, three generic medications: valsartan (brand name: Diovan), losartan (brand name: Cozaar), and irbesartan (brand name: Avapro). If you or someone you love took losartan and were diagnosed with cancer, get in touch with a qualified attorney as soon as possible to start building a case against those who were responsible. What element in losartan can cause cancer? In March, the FDA raised concerns about losartan potassium tablets sold by India-based Hetero Labs Ltd. and distributed by Camber Pharmaceuticals. according to data provided by the U.S. Government. Losartan Cancer Lawsuit. Hundreds of lots of losartan drugs and others in its class have been recalled by more than a dozen drug manufacturers since impurities were first discovered in mid-2018. The centralized lawsuits arise from ongoing recalls involving a class of heart and blood-pressure medications known as angiotensin II receptor blockers (ARBs), including valsartan, irbesartan, and losartan. Eventually, Losartan became the first successful angiotensin II antagonist drug in 1986. The makers of losartan drugs have put patients at risk by making and selling a defective drug. Valsartan Recall: What you should know. Expands Voluntary Nationwide Recall of Losartan Potassium to 50 mg and 100 mg Tablets USP, Sold … Our lawyers are investigating potential lawsuits on behalf of people who were diagnosed with cancer or other severe side effects after taking recalled Losartan medications. In April 2019, Torrent Pharmaceuticals Ltd. recalled Losartan Potassium Tablets USP and Losartan Potassium/Hydrochlorothiazide Tablets, USP due to the detection of the impurity N-Nitroso-N-methyl-4-aminobutyric acid (NMBA). Contact a Sullo & Sullo hydrochlorothorazide lawyer today, for highly qualified legal assistance with your amlodipine recall lawsuit. The prescribing sheet for Cozaar warns that patients with kidney issues may be at risk of developing acute renal failure while taking losartan. Losartan Recall Lawsuit In November 2018, the FDA issued a recall of Losartan after detecting trace amounts of the probable human carcinogen N-nitrosodiethylamine (NDEA). Since then, consumers have filed individual lawsuits and class action suits against valsartan manufacturers and distributors. The Eichholz Law Firm, P.C. Resulting oligohydramnios can be associated with fetal lung hypoplasia and skeletal deformations. To that end, let’s explore the biggest, ongoing FDA recalls and lawsuits. This website provides the facts regarding the Valsartan lawsuits, settlements, and recalls. That is the “carcinogenic” or cancer-causing impurity known as N-nitrosodiethylamine (NDEA). Adults use this drug to treat high blood pressure and congestive heart problems as well as ventricle dysfunction after suffering a heart attack. The recall involves losartan and potassium/hydrochlorothiazide combination pills found to contain N-Nitroso-N-methyl-4-aminobutyric acid, or NMBA, according to a … Nice, Professional Staff from the beginning to the end. “Over the past few months, the FDA has conducted a major investigation and has worked with drug companies to address the presence of impurities in these products,” said FDA Commissioner Scott Gottlieb. In July 2018, the U.S. Food and Drug Administration (FDA) announced the recall of several generic valsartan drugs. Sonstiger Bestandteil mit bekannter Wir-kung: Jede Filmtablette enthält 18,0 mg Lactose-Monohydrat. The drug works to treat high blood pressure by blocking a hormone called angiotensin II. Losartan-ratiopharm® 100 mg Filmtabletten 1 1. Losartan Recall Expanded by FDA Over Cancer Concerns September 26, 2019. As a result, Losartan is one of the most popular drugs used to treat this condition and in turn, diminish the likelihood of strokes. If you or a loved one has experienced a health problem after receiving the drug Valsartan or Losartan, we want to hear from you. It was first approved in many European countries in 1996, and in the US in 1997. After several recalls were issued regarding potential carcinogens tainting popular blood pressure medications, it didn’t take long before the first lawsuits were filed. Losartan is considered a generic angiotensin II receptor blocker (ARB), and is primarily used to treat high blood pressure or heart failure. 6 likes. Valsartan lawsuits claim contamination with toxic chemicals, including N-nitrosodimethylamine (NDMA) and N-Nitrosodiethylamine (NDEA), caused health problems while others demand compensation for the tainted medicine they bought. Losartan Recall Class Action Lawsuit March 1, 2019 – New Jersey-based Camber Pharmaceuticals, Inc. has issued a nationwide recall for 87 lots of the blood pressure medication Losartan to the consumer level after routine tests found the product to be contaminated with a potential carcinogen (cancer-causing substance). Learn more about the background of losartan and its possible side effects. The Eichholz Law Firm has years of experience in dealing with drug-related injuries, and our experts can help you seek compensation and the justice you deserve. I would recommend this firm and I will certainly use them again in the future if need be. Previously, taking losartan was discouraged during the second and third trimesters but losartan could pose a danger to the fetus earlier in the pregnancy as well. Losartan potassium, a non-peptide molecule, is chemically described as 2-butyl-4-chloro-1-[p-(o-1H-tetrazol-5-ylphenyl)benzyl]imidazole-5-methanol monopotassium salt. Of all the varieties of recalls issued by the FDA, class 1 is the most severe and is limited to situations where the recalled product “will cause serious adverse health consequences or death.” Eventually, other ARBs were developed using losartan as a basis. On Sept. 23, 2019 the Food and Drug Administration issued a voluntary nationwide recall of a popular and widely-prescribed blood pressure medication due to a cancer-related contamination. That’s why it was so devastating when tens of thousands of people found out that the losartan-containing drugs they were taking to save their lives were contaminated with cancer-causing substances. The US Food and Drug Administration (FDA) began recalling hundreds of products containing Valsartan in July 2018 due to contamination with carcinogens (chemicals that cause cancer ). The FDA recalled dozens of products that contained Losartan due to an impurity in the active ingredient - the impurity is classified as a probable human carcinogen. It was the ninth most prescribed drug in the United States in 2016 with nearly 50 million prescriptions, according to data provided by the U.S. Government. Torrent Pharmaceuticals Ltd. has expanded its recall of losartan potassium and losartan potassium/hydrochlorothiazide tablets. Losartan recalls due to amounts of NMDA and NDEA have been issued in prior recall notices. Valsartan Recall Lawsuit. Losartan Recall. Losartan Recall Lawsuit Losartan is a popular blood pressure medication that has been voluntarily recalled multiple times due to the presence of a human carcinogen. A widespread recall of common blood pressure and heart failure medications has been expanded to include more drugs containing losartan due to an "impurity" that may pose a cancer risk. A-S Medication Solutions LLC (Teva/Actavis & Prinston/Solco) This is the fifth time the company has expanded its voluntary recall of losartan in 2019. The class 1 recall included the medications Valsartan, Losartan, and Irbesartan and was one of the largest in the history of the FDA. In a matter of mere months, the previously little-known pharmaceutical ingredient valsartan has gone from relative obscurity to being at the center of multiple drug recalls and at least one potential class-action lawsuit. Last week, another blood pressure drug recall was announced, the third since July. Losartan Recalls. The FDA recalled Valsartan after finding the probable human carcinogen NDMA had contaminated the drug. Get a Free Case Review Now Start Here Current Valsartan Lawsuits. It belongs to a family of medications called angiotensin II receptor blockers (ARBs). After the initial valsartan recall was announced, some doctors switched their patients to losartan, which is in the same class of blood pressure medications (angiotensin II receptor blockers, or ARBs). Valsartan Recall Lawsuit. More than 20 health agencies around the world issued similar valsartan recalls at … Losartan is the latest drug to be recalled for possible nitrosamine contamination, a class of chemicals that may cause cancer. The FDA investigation is still ongoing. So far, none of the drugmakers of Losartan have received reports of adverse effects related to the recall and presence of carcinogenic substances. One of the first losartan recalls was issued by Sandoz Inc in November 2018 after NDEA was found in the drug. In early March 2019, the FDA expressed concern about yet another cancer-causing substance present in ARBs. These include dizziness, upper respiratory infection, nasal congestion, and back pain. Joe Lyon is a highly-rated Cincinnati, Ohio product liability attorney and Losartan lawyer investigating Losartan recall lawsuits and cancer risks for plaintiffs nationwide. NDEA is considered a probable human carcinogen by the International Agency for Research on Cancer (IARC). 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