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[PDF File]Recall of Losartan by Major
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Jan 15, 2019 · Recall of Losartan by Major Effective Date: January 11, 2019 On January 11, 2019, Major announced a voluntary recall of one lot of unit dose Losartan tablets because of the presence of trace amounts of an unexpected impurity, N-nitrosodiethylamine (NDEA), found in the finished product. NDEA is classified as a probable human carcinogen.
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[PDF File]HSA RECALLS THREE BRANDS OF LOSARTAN MEDICINES …
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Not all losartan medicines are affected by this recall. Only three out of the ten losartan products in Singapore contain unacceptable levels of nitrosamine impurity. ... As losartan is used to treat high blood pressure, stopping the ... with a replacement brand of losartan or a different medicine by your healthcare
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[PDF File]RECALL OF 3 BRANDS OF LOSARTAN MEDICINES: ADVISORY …
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RECALL OF 3 BRANDS OF LOSARTAN MEDICINES: ADVISORY FOR PATIENTS ... Seven other brands of losartan medicine approved in Singapore are not affected by the recall. 2. About 137,000 patients in Singapore are using the three recalled brands of losartan ... more during the interim period should they switch to replacement medications, which will
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[PDF File]Recall of 3 brands of Losartan Medicines Frequently Asked ...
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Recall of 3 brands of Losartan Medicines Frequently Asked Questions 1. Which are the high blood pressure medicines recalled by the Health Sciences Authority? The Health Sciences Authority (HSA) has recalled three brands of high blood pressure medicine which contain losartan – Losartas, Losagen and Hyperten – on 28 March 2019.
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[PDF File]Recall of Losartan by AvKARE Effective Date: April 23, 2019
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Recall of Losartan by AvKARE Effective Date: April 23, 2019 On April 23, 2019, AvKARE announced an expansion to the voluntary recall of some lots of Losartan tablets ... obtain a replacement, and advised to continue their current therapy until they obtain a replacement or
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[PDF File]Voluntary recall of Losartan-containing drugs - Health
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Mar 22, 2019 · Voluntary recall of Losartan-containing drugs - Health Canada Notice On March 9, 2019, Health Canada advised Canadians that multiple lots of drugs containing losartan had been voluntarily recalled by Teva Canada, Apotex Inc., Pharmascience Inc., and Pro Doc Limitée due to the potential for a nitrosamine impurity, N-nitroso-N-
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[PDF File]Sandoz – Recall of Losartan/Hydrochlorothiazide
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Sandoz – Recall of Losartan/Hydrochlorothiazide • On November 8, 2018, Sandoz announced a voluntary, consumer-level recall of one lot of losartan/hydrochlorothiazide (HCTZ) tablets due to the detection of trace amounts of an unexpected impurity, identified as n-nitrosodiethylamine (NDEA) contained in the active pharmaceutical
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[PDF File]HSA RECALLS THREE BRANDS OF LOSARTAN MEDICINES …
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3 Not all losartan medicines are affected by this recall. Only three out of the ten losartan products in Singapore contain unacceptable levels of nitrosamine impurity. ... stopping the medicine without replacement of other equivalent medication can ... with a replacement brand of losartan or a different medicine by your healthcare
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[PDF File]Valsartan recall Angiotensin II Receptor Blockers (ARBs ...
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Valsartan recall Angiotensin II Receptor Blockers (ARBs) equivalent dosing Valsartan (Diovan) is supplied in doses of 40, 80, 160, and 320 mg tablets. ... Losartan* (Cozaar) 25 mg 50 mg 100 mg -- Olmesartan (Benicar) 10 mg 20 mg 20 to 40 mg 40 mg
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Drug recall notice for losartan and losartan-containing ...
Drug recall notice for losartan and losartan-containing drug products . The U.S. Food and Drug Administration (FDA) has issued recalls for losartan tablets due to an impurity in the manufacturing of these medicines. The FDA continues to monitor drugs in the angiotensin II
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Replacement for losartan recall