Torrent Pharmaceuticals is expanding a recall of blood-pressure medication possibly tainted with a cancer-causing chemical. On Sept. 23, 2019 the Food and Drug Administration issued a voluntary nationwide This recall is due to an impurity called N-nitrosodiethylamine (NDEA) in some products that contain losartan, valsartan or irbesartan. ... It’s unclear exactly what the cancer risk is if … ©2021 FOX News Network, LLC. voluntary recall of two lots of losartan potassium 100 mg tablets due to N-Nitrosodiethylamine (NDEA) in the losartan active pharmaceutical ingredient (API) manufactured by Hetero Labs Limited. In the end, the study found the overall cancer risk for someone exposed to NDMA in valsartan was no greater than someone who was not exposed. In July 2018, valsartan was the first blood pressure drug recalled. Valsartan, Irbesartan, and Losartan are among the most commonly prescribed drugs for treating high blood pressure and heart failure. This material may not be published, broadcast, rewritten, Torrent Pharmaceuticals says two of its blood pressure medications were found to have trace amounts of a potentially cancer … This is the third blood pressure drug to have been recalled due to possible cancer risk. Mutual Fund and ETF data provided by Refinitiv Lipper. This recall is due to an impurity called N-nitrosodiethylamine (NDEA) in some products that contain losartan, valsartan or irbesartan. 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. Losartan is used to treat high blood pressure (hypertension). Losartan Recall – What is the Cancer-Causing Ingredient It was indicated that Losartan tablets contain N-methylnitrosobutyric acid (NMBA). The FDA is recalling losartan, a blood pressure drug made by Sandoz, due to possible cancer concerns after contamination by the chemical NDEA was found. The recall affects Losartan Potassium tablets USP in 25, 50 and 100 mg doses. More than 20 countries were affected by the recall over possible cancer-causing impurity concerns. Sandoz Inc. is voluntarily recalling losartan potassium hydrochlorothiazide tablets because the pills could contain an impurity N-nitrosodiethylamine (NDEA). This recall … Quotes displayed in real-time or delayed by at least 15 minutes. In November 2018, the FDA issued a recall of Losartan after detecting trace amounts of the probable human carcinogen N-nitrosodiethylamine (NDEA). The contaminated medication was not distributed before Oct. 8. Now people who have developed cancer after taking Losartan may be able to file lawsuits. For more about the newly recalled lots, read the pharmaceutical company's announcement at FDA.gov. This is the third blood pressure drug to have been recalled due to possible cancer risk. Mutual Fund and ETF data provided by Refinitiv Lipper. Legal Statement. More: FDA chief: Blood pressure medicine recalls reflect increased scrutiny on drug safety. Madeline Farber is a Reporter for Fox News. However, as of July 2018, the Food and Drug Administration (FDA) has issued a Following is a list of possible medication recalls, market withdrawals, alerts and warnings. Losartan potassium tablets sold by Macleods Pharmaceuticals were recalled after trace amounts of a probable carcinogen known as NMBA were found in the popular blood-pressure medicine. The recall of a widely-prescribed blood pressure drug losartan is being expanded again by the Food and Drug Administration due to contamination by cancer-linked chemical. “Patients who are taking Losartan Potassium Tablets, USP and Losartan Potassium/Hydrochlorothiazide Tablets, USP should continue taking their medication, as the risk of harm to the patient’s health may be higher if the treatment is stopped immediately without any alternative treatment,” the FDA said, advising patients to contact their pharmacist or doctor about an alternative medication. Learn more about the background of losartan and its possible side effects. Torrent Pharmaceuticals Ltd. has expanded its recall of losartan potassium and losartan potassium/hydrochlorothiazide tablets. Since July 2018 numerous batches have been recalled due to cancer-causing NDMA and NDEA impurities from contaminated manufacturing facilities in China and India. Losartan potassium tablets sold by Macleods Pharmaceuticals were recalled after trace amounts of a probable carcinogen known as NMBA were found in the popular blood-pressure medicine. Losartan Recalls Issued In June 2018, the FDA found that some generic versions of the angiotensin II receptor blocker (ARB) valsartan contained impurities. Quotes displayed in real-time or delayed by at least 15 minutes. losartan FDA Alerts. The recall was prompted by the discovery of cancer-causing impurities in the medications. In a Sept. 19 statement, the Food and Drug Administration (FDA) announced Torrent Pharmaceuticals Limited voluntarily expanded the recall to include additional lots of its Losartan Potassium Tablets USP and Losartan Potassium/hydrochlorothiazide tablets, which are used to treat hypertension, hypertensive patients with Left Ventricular Hypertrophy, and nephropathy in Type 2 diabetic patients. Torrent Pharmaceuticals Limited has again expanded a recall of its blood pressure medication over concerns the tablets contain small amounts of a cancer-causing ingredient. or redistributed. Market data provided by Factset. This material may not be published, broadcast, rewritten, or redistributed. The active pharmaceutical ingredient (the real medicine) was made in China by Zhejiang Huahai Pharmaceutical Co. Ltd., the same Chinese company that made the contaminated valsartan. Fox News' Alexandria Hein contributed to this report. The ingredient detected in the tablets was identified as N-Methylnitrosobutyric acid (NMBA), a known animal and potential human carcinogen. A recall on losartan medications soon followed. The company said the recall only affects products found to have more than the FDA-allowable amount of NMBA. MedWatch Safety Alerts are distributed by the FDA and published by Drugs.com. 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. 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. More than 20 health agencies around the world issued similar valsartan recalls at the same time. Torrent Pharmaceuticals Ltd. has expanded its recall of losartan potassium and losartan potassium/hydrochlorothiazide tablets. The valsartan recall was prompted by the discovery of a cancer-causing substance in the medications. Macleods Pharmaceuticals Limited is recalling 32 lots of the popular blood pressure drug losartan after discovering trace amounts of a probable carcinogen. Talk about which losartan tablets are recalled and what to do about it. The substance is a probable human carcinogen, according to the International Agency for Research on Cancer. Branham indicates she ingested some of the recalled valsartan and losartan drugs before she was diagnosed with kidney cancer in August 2017, which ultimately led to the need for a partial nephrectomy. Stay up-to-date on the biggest health and wellness news with our weekly recap. NDEA can cause cancer, even in small amounts. Powered and implemented by FactSet Digital Solutions. Individuals who used these drugs and were diagnosed with cancer may be eligible for … The fourth was announced in April. The United States Food and Drug Administration (FDA) is recalling losartan, a blood pressure medication, after finding contamination that could cause cancer. The expanded recall includes an additional three lots of losartan potassium tablets USP and two lots of losartan potassium/ydrochlorothiazide … Market data provided by Factset. The team also looked at the cancer development of these patients during the span of the study. Over the summer, blood pressure drug valsartan was similarly recalled. “FDA is alerting patients and health care professionals to Sandoz’s voluntary recall of one lot – JB8912 – of losartan potassium and hydrochlorothiazide 100mg/25mg tablets, that contain losartan, an angiotensin II receptor blocker (ARB), and hydrochlorothiazide, a diuretic, used in combination for the treatment of hypertension. In September 2019, Torrent Pharma expanded a recall for Losartan after tests detected a cancer-causing impurity called NMBA. Valsartan, Losartan & Irbesartan Recalled Due to Cancer Risk The U.S. Food and Drug Administration (FDA) is recalling a number of high blood pressure medications over potential cancer risks. Many patients that were on Valsartan were switched over to Losartan after Valsartan was recalled in July 2018. NDEA appears to cause cancer in animals and is suspected to cause cancer in humans, according to lab tests. Sandoz Inc. is voluntarily recalling losartan potassium hydrochlorothiazide tablets because the pills could contain an impurity N-nitrosodiethylamine (NDEA). One lot of Losartan tablets, used to treat high blood pressure, has been recalled by Sandoz because it includes “a trace amount” of N-nitrosodiethylamine, commonly referred to as NDEA. Losartan affected by the recall are 100 milligram/25 milligram tablets with the lot number JB8912. Using recall data, the research team estimated the number of participants exposed to NDMA. The phase IV clinical study is created by eHealthMe based on reports of 107,313 people who have side effects when taking Losartan from the FDA, and is updated regularly. Camber Pharmaceuticals, Inc. is recalling 87 lots of Losartan Tablets USP 25 mg, 50 mg, and 100 mg to consumer level. Check out what's clicking on Foxnews.com. Find out which specific blood pressure medications are affected by the recall The recall involves losartan and potassium/hydrochlorothiazide combination pills found to contain N-Nitroso-N-methyl-4-aminobutyric acid, or NMBA, according to a … This prompted the first recall of valsartan medicines due to the presence of a cancer-causing substance called N-nitrosodimethylamine (NDMA) in July 2018. Company Announcement. Many patients that were on Valsartan were switched over to Losartan after Valsartan was recalled in July 2018. You've successfully subscribed to this newsletter! Update [6/26/2019] FDA is alerting patients and health care professionals to Macleods Pharmaceuticals’ voluntary recall of two lots of losartan potassium tablets (50mg strength) and 30 lots of losartan potassium/hydrochlorothiazide (HCTZ) combination tablets (12 lots of 50mg/12.5mg strength, three lots of 100mg/12.5mg strength, and 15 lots of 100mg/25mg … Contact a Sullo & Sullo hydrochlorothorazide lawyer today, for highly qualified legal assistance with your amlodipine recall lawsuit. Valsartan is a similar blood pressure medication to losartan. These were sold in America nationwide at the consumer level as 100 mg/25 mg tablets. Valsartan and Losartan Recalled Due to Risk of Causing Cancer Valsartan and Losartan are two of the most commonly-prescribed high blood pressure medications, however, the side effects may outweigh the benefits. In November 2018, the FDA issued a recall of Losartan after detecting trace amounts of the probable human carcinogen N-nitrosodiethylamine (NDEA). All rights reserved. Fox News Flash top headlines for Sept. 24. In July, drug companies began recalling dozens of lots of the blood pressure and heart medications called valsartan, losartan and irbesartan after … “The risk of developing cancer in a few patients following long-term use of the product cannot be ruled out,” the FDA noted. More specifically, the expanded recall includes “an additional 3 lots of Losartan Potassium Tablets USP and 2 lots of Losartan Potassium/Hydrochlorothiazide Tablets, USP,” the FDA said in a statement. 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 … The losartan recall involves one lot of 1,000-count plastic bottles of Losartan Potassium Hydrochlorothiazide, NDC 0781-5207-10, Lot number JB8912. The company stated that the affected products found to include more NMBA than the FDA allowed. Legal Statement. It is an animal and human carcinogen. The Sandoz Inc. recall involved 100 milligram/25 milligram Losartan tablets with the lot number JB8912 and expiration date of June 2020. Recalled Losartan Caused Colon Cancer Diagnosis, Lawsuit Alleges September 16, 2019 ... Side effects of Belviq may increase the risk of cancer, resulting in a diet drug recall and lawsuits. Losartan Recall Lawsuit. ©2021 FOX News Network, LLC. Powered and implemented by FactSet Digital Solutions. Discussion of the losartan recall and the associated cancer risk. The latest round was announced on June 25, with a Macleods Pharmaceutical Limited Losartan Potassium and Losartan Potassium/Hydrochlorothiazide combination recall affecting 32 lots in total. Summary: Bladder cancer is found among people who take Losartan, especially for people who are male, 60+ old, have been taking the drug for 1 - 2 years. Vivimed Life Sciences Pvt Ltd issued the recall on 19 lots of the medication due to a cancer-causing impurity. BLOOD PRESSURE MEDICATION RECALL EXPANDED OVER POSSIBLE CANCER-CAUSING INGREDIENT. Losartan Recall Lawsuit. Follow Ashley May on Twitter: @AshleyMayTweets, More: Blood pressure drug recalled for possible cancer risk, FDA says, More: FDA to limit sale of sweet-flavored e-cigarettes in hope of curbing teen vaping 'epidemic', FDA chief: Blood pressure medicine recalls reflect increased scrutiny on drug safety, recall for blood pressure medication irbesartan, Blood pressure drug recalled for possible cancer risk, FDA says, FDA to limit sale of sweet-flavored e-cigarettes in hope of curbing teen vaping 'epidemic', Your California Privacy Rights/Privacy Policy. Losartan Recall . Patients with questions about the recall can contact Sandoz Inc. at 800-525-8747 or email usdrugsafety.operations@novartis.com. Losartan Recall . What you should do Media enquiries Public enquiries March 9, 2019 For immediate release. You can follow her on Twitter @MaddieFarberUDK. Search List of Recalled Angiotensin II Receptor Blockers (ARBs) including Valsartan, Losartan and Irbesartan. Fox News Flash top headlines for Sept. 24 are here. Patients who are currently taking this medication are advised to speak with their doctor before stopping use, because the risk of going off of the medication might be greater than the possible cancer risk, according to the Nov. 8 recall notice. NDEA appears to cause cancer in animals and is suspected to cause cancer in humans, according to lab tests. Sandoz Inc. is voluntarily recalling losartan potassium hydrochlorothiazide tablets because the pills could contain an impurity N-nitrosodiethylamine (NDEA). The losartan recall is from the generic drug company Sandoz, which is a subsidiary of Novartis, a Swiss multinational pharmaceutical company. All rights reserved. Distribution of generic Zantac halted 03:00. Note: This story was updated on Sept. 23, 2019, with an additional losartan recall from Torrent Pharmaceuticals. OTTAWA – Health Canada is advising Canadians that multiple lots of Losartan-containing drugs are being voluntarily recalled by Teva Canada, Apotex Inc., Pharmascience Inc., and Pro Doc Limitée because of the potential for a nitrosamine impurity, N-Nitroso-N-methyl-4-aminobutyric acid (NMBA). BLOOD PRESSURE MEDICATION RECALL EXPANDED OVER POSSIBLE CANCER-CAUSING INGREDIENT . Recently, the FDA issued a recall for blood pressure medication irbesartan, also because of a NDEA contamination concern. The U.S. losartan recall cancer and drug Administration announced a third blood pressure medication to losartan after detecting trace of. Who have developed cancer after taking losartan may be specifically about losartan or relate to a group or of... ) in some products that contain losartan, valsartan was the first blood pressure drugs has expanded... Generic drug company sandoz, which is a similar blood pressure drug to have been recalled due an... 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