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Worldwide blood pressure medicine recall expanding. Additionally, Legacy expanded its recall to include one additional lot of losartan tablets made with API manufactured by Hetero Labs. Patients who are on Losartan Potassium Hydrochlorothiazide should continue taking their medication, as the risk of harm to a patient’s health may be higher if the treatment is stopped immediately without any alternative treatment. Losartan is now the third “sartan” drug that has been recalled after the carcinogen N-Nitrosodiethylamine (NDEA) was detected in its active pharmaceutical ingredient. Of these, about 130,000 patients have been … Here’s what to watch out for. Follow our blog at www.sandoz.com/makingaccesshappen. 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. Another blood pressure medication has been recalled over concerns it could contain trace amounts of carcinogens. Losartan, irbesartan, and other “-sartan” drugs are also part of this class of drugs. Dozens of blood pressure medications have been recalled since the first products were pulled off the shelf in July 2018 due to impurities. Before sharing sensitive information, make sure you're on a federal government site. Herald Staff [email protected] A massive recall of some of the world’s leading brands of hypertension medication continues. This impurity, which is a substance that occurs naturally in certain foods, drinking water, air pollution, and industrial processes, has been classified as a probable human carcinogen as per International Agency for Research on Cancer (IARC). Legacy Pharmaceutical Packaging LLC is notifying its distributors and customers in writing and is arranging/assisting for the return of all recalled products to Inmar Pharmaceutical Services. Novartis is providing the information in this press release as of this date and does not undertake any obligation to update any forward-looking statements contained in this press release as a result of new information, future events or otherwise. The recall covers 25 mg, 50 mg and 100 mg dosages. Torrent Pharmaceuticals voluntarily recalled two lots of losartan potassium tablets because of trace amounts of an impurity that has been found … Teva is recalling lots of losartan-containing medication that tested positive for NMBA above 9.82 parts per million. 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. Sandoz is headquartered in Holzkirchen, in Germany’s Greater Munich area. Disclaimer ", MacBook Pro recall: Apple voluntarily recalling batteries on MacBook Pro notebooks due to safety risk, Rock 'n Play recall: Fisher-Price recalls 4.7 million infant sleepers after reported death. If you're concerned you may be taking recalled losartan, compare the information on your prescription drug label with the information in the table. FDA: Blood pressure medication Losartan recalled due to cancer concern. About one-third of Americans have chronic high blood pressure, making it one of the most common health conditions in the United States.Recently, popular medications to treat high blood pressure have been under scrutiny by the FDA for containing cancer-causing impurities.. They were manufactured by these drug companies: What brand of losartan has been recalled? In particular, our expectations regarding such products could be affected by, among other things, the uncertainties inherent in research and development, including clinical trial results and additional analysis of existing clinical data; regulatory actions or delays or government regulation generally; global trends toward health care cost containment, including government, payor and general public pricing and reimbursement pressures; our ability to obtain or maintain proprietary intellectual property protection; the particular prescribing preferences of physicians and patients; general political and economic conditions; safety, quality or manufacturing issues; potential or actual data security and data privacy breaches, or disruptions of our information technology systems, and other risks and factors referred to in Novartis AG’s current Form 20-F on file with the US Securities and Exchange Commission. Torrent Pharmaceuticals Limited has expanded its recall of Losartan potassium tablets USP. Patients should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using Losartan Potassium Hydrochlorothiazide. (FiercePharma) FDA losartan recall: Cancer risk tied to blood pressure drug losartan. Only three of the ten losartan products in Singapore – Hyperten, Losagen and Losartas – contain the nitrosamine impurity. Our portfolio of approximately 1000 molecules, covering all major therapeutic areas, accounted for 2017 sales of USD 10.1 billion. STOCK PHOTO/Getty Images. (I was also on Cozaar and then Avapro). About Sandoz Over 50 Companies Have Recalled Losartan, Valsartan Since July. The FDA has compiled a list of all the … The pills have been flagged for … More Recalls, Market Torrent and Hetero/Camber are only recalling lots of losartan-containing medication with NMBA above the interim acceptable intake limits of 0.96 parts per million (ppm). Consult your healthcare provider if you are unsure if you are taking an affected brand. Company Announcement. According to the FDA , about 300 lots of losartan and losartan/hydrochlorothiazide products have been recalled as of April 18, 2019. This is the fifth time in 2019 that Torrent Pharmaceuticals has expanded its voluntary recall of losartan. Should one or more of these risks or uncertainties materialize, or should underlying assumptions prove incorrect, actual results may vary materially from those set forth in the forward-looking statements. They were found to contain higher than accepted levels of a nitrosamine impurity, N-nitroso-N-methyl-4-aminobutyric acid (NMBA). 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