losartan potassium recalls biaxin

NMBA is a "potential human carcinogen," the The recall comes amid a larger string of recalls of blood pressure medications valsartan, losartan and irbesartan that contain trace levels of carcinogens NMBA, N-Nitrosodimethylamine (NDMA) and N-Nitrosodiethylamine (NDEA), the FDA says.Hundreds of lots of the medication have been recalled since last July.The drugs, angiotensin II receptor blockers (ARBs), work by widening or relaxing blood vessels, thus lowering blood pressure.

The recall involves losartan and potassium/hydrochlorothiazide combination pills found to contain N-Nitroso-N-methyl-4-aminobutyric acid, or NMBA, according to a "Based on the available information, the risk of developing cancer in a few patients following long-term use of the product cannot be ruled out," the notice stated. Find out which specific blood pressure medications are affected by the recall Losartan comes only as an oral tablet. However, not all ARBs have been affected, and patients should continue to use their medication, the FDA says. The manufacturing change may generate the contaminants "when specific chemicals and reaction conditions are present" and can result of reusing materials such as solvents.In January, the agency admitted that some versions of the drug valsartan contained However, FDA officials said the cancer risk for any person who took valsartan that had the carcinogen N-nitrosodimethylamine, or NDMA, is small. Losartan potassium 25 mg, 50 mg and 100 mg tablets contain potassium in the following amounts: 2.12 mg (0.054 mEq), 4.24 mg (0.108 mEq) and 8.48 mg (0.216 mEq), respectively.

FDA scientists concluded there would be one more cancer case above average rates for every 8,000 people on the highest dose of valsartan for four years. The latest recall is the second for the same reason by Macleods Pharmaceuticals, which in February Since 2018, there have been at least 19 recalls by manufacturers of versions of losartin over cancer fears, including a March recall of 87 lots of losartin made by Camber Pharmaceuticals. Add Other Info Comment The dosage can be increased after 3 weeks of therapy to a maximum of 100/25 (losartan 100 mg/hydrochlorothiazide 25 mg) once daily as needed to control blood pressure [see Clinical Studies (14.2)].

2.1 Hypertension The usual starting dose of losartan potassium and hydrochlorothiazide tablets are 50/12.5 (losartan 50 mg/hydrochlorothiazide 12.5 mg) once daily.

Americans who take prescription drugs to control blood pressure should check their medical cabinets once again.

A recall of common blood pressure medication losartan has been expanded for a fifth time after manufacturer Torrent Pharmaceuticals found a possibly carcinogenic impurity in … The recall involves losartan and potassium/hydrochlorothiazide combination pills found to contain N-Nitroso-N-methyl-4-aminobutyric acid, or NMBA, according to a … A recall of common blood pressure medication losartan has been expanded for a fifth time after manufacturer Torrent Pharmaceuticals found a possibly carcinogenic impurity in more batches of the drug, federal health officials said.Three additional lots of losartan potassium tablets and two additional lots of losartan potassium/hydrochlorothiazide tablets were The lots contained levels of N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) above the acceptable daily intake levels determined by the FDA.

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Get the latest breaking news delivered straight to your inbox.Copyright © 2020 CBS Interactive Inc. All rights reserved. Losartan Potassium / Hydrochlorothiazide, USP 50mg/12.5mg, 90 count, batch No. It’s also used to treat diabetic nephropathy, and to reduce stroke risk. Losartan is a prescription drug used to treat hypertension (high blood pressure).