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Three drug companies recalled 126 lots of the blood pressure drugs losartan and valsartan this ... AurobindoPharma recalled 40 mg, 80 mg, 160 mg and 320 mg tablets that were distributed to ...
This covers lot No. JB8912 of Losartan Potassium Hydrochlorothiazide 100 mg or 25 mg tablets in 1,000-count bottles, expiration date 06/2020. None of the recalled tablets were distributed before ...
Losartan tablets have been approved in 25-mg, 50-mg, and 100-mg doses, and losartan/hydrochlorothiazide combination tablets will be available in 50-mg/12.5-mg, 100-mg/12.5-mg, and 100-mg/25-mg ...
That new could-be carcinogen, N-Methylnitrosobutyric acid (NMBA), caused Camber Pharmaceuticals to recall an additional 87 lots of Losartan potassium tablets Thursday. Friday, Torrent recalled 60 ...
Drug repackager Legacy Pharmaceutical Packaging is recalling 40 repackaged lots of Losartan Tablets USP 25 mg, 50 mg and 100 mg to the consumer level because they were made with an API in which ...
Andersson and Neldam [5] evaluated candesartan cilexetil 8 and 16 mg vs. losartan 50 mg and found that candesartan cilexetil 16 mg once daily (n=84) reduced trough DBP more effectively than ...
18 Atenolol (at an initial dose of 0.5 mg per ... the losartan group in the overall rate of adverse events (408 events and 365 events, respectively; P=0.10) or serious adverse events (40 events ...
The first dose of telmisartan or losartan was 40 or 50 mg per day, respectively. If the patient's BP did not reach the BP target, the doses were increased to 80 or 100 mg per day, respectively.
A total of 1513 patients were enrolled in this randomized, double-blind study comparing losartan (50 to 100 mg once daily ... accounting for approximately 40 percent of all cases in the United ...
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