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FDA Recalls Blood Pressure Drug Losartan for Contamination.

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. Sep 23, 2019 · A recall of common blood pressure medication losartan has been expanded for a fifth time after manufacturer Torrent Pharmaceuticals found. Apr 24, 2019 · The FDA will allow some versions of losartan with a carcinogen to be shipped to pharmacies to avert a shortage of the critical medication. ☀️☕📧 = 😊 Florida Man headlines Most. Sep 24, 2019 · The recall applies only to lots that contain levels of NMBA above FDA-allowable levels. Monday was the fifth time the FDA has expanded the losartan.

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. Jan 03, 2019 · According to the FDA, on Tuesday, Torrent has not received any reports of adverse events related to the company's Losartan recall. Consumers should contact their physician or health care provider if they have experienced any problems that may be related to taking or using this drug.

Mar 26, 2019 · The U.S. Food and Drug Administration has updated its lists of valsartan and losartan-containing blood pressure medicines under recall due to the. Doctors prescribe losartan for patients with high blood pressure and for Type 2 diabetics who have nephropathy. The FDA advises patients who take these drugs — even the ones that have been. Losartan is a popular drug to treat high blood pressure Recall comes after another hypertension drug was recalled CHECK YOUR MEDICATION: Head to the FDA website for information on losartan.

Apr 19, 2019 · Torrent Pharmaceuticals Ltd. has expanded its recall of losartan potassium and losartan potassium/hydrochlorothiazide tablets. Jun 26, 2019 · Macleods also recalled one lot of the losartan combination drug in February for the same reason. The company said in the statement that for this recall "it. Nov 13, 2019 · Update [11/9/2018] 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. Sandoz’s product was made using an active.

Updated FDA list of recalled blood pressure drugs.

Losartan blood pressure medication recall expanded again.

Nov 13, 2018 ·: “Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Losartan Potassium and Hydrochlorothiazide Due to the Detection of Trace Amounts of NDEA N-Nitrosodiethylamine Impurity. FDA: Voluntary recall of losartan blood pressure drug expanded. Updated Jan 29, 2019; Posted Jan 24, 2019. Torrent Pharmaceuticals Limited is expanding its voluntary recall from 10 lots of.

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