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  2. ARB Recalls: Valsartan, Losartan and Irbesartan

    www.fda.gov/drugs/drug-safety-and-availability/recalls-angiotensin-ii-receptor...

    Some manufacturers are recalling some medications containing amlodipine in combination with valsartan or losartan, and some medications containing hydrochlorothiazide HCTZ in combination with...

  3. FDA Updates & Press on ARB Recalls: Valsartan, Losartan and...

    www.fda.gov/drugs/drug-safety-and-availability/fda-updates-and-press...

    FDA has updated lists of valsartan products under recall and valsartan products not under recall. Additionally, FDA reminds patients taking this medication or any recalled ARB to continue...

  4. On July 13, 2018, the FDA announced a voluntary recall of some valsartan products because of contamination with NDMA, a potentially cancer-causing chemical. Other drugs affected by the valsartan recall include losartan and irbesartan.

  5. Search List of Recalled ARBs: Valsartan, Losartan and Irbesartan

    www.fda.gov/drugs/drug-safety-and-availability/search-list-recalled...

    Drug Safety and Availability. Search List of Recalled Angiotensin II Receptor Blockers (ARBs) including Valsartan, Losartan and Irbesartan. Find out which specific blood pressure medications are...

  6. After multiple recalls, FDA approves new generic for valsartan

    www.cbsnews.com/news/valsartan-generic-approved-after-drug-recalls-fda...

    The U.S. Food and Drug Administration has approved a new generic of the blood pressure medication valsartan to help alleviate a recent shortage due to multiple safety recalls.

  7. Valsartan-Containing Products Recalled By Some Manufacturers

    www.express-scripts.com/notices/recall/valsartan-containing-products-recalled...

    On July 13th, the FDA announced a recall of medications containing Valsartan, a generic medication used to treat high blood pressure and heart failure from multiple manufacturers due to an impurity (NDMA) detected in the recalled products.

  8. RemedyRepack recalls several lots of generic valsartan. The FDA releases a testing method to detect NDMA. Manufacturers can use this test to determine if their medications and ingredients are safe for consumers.

  9. Current Status of Angiotensin Receptor Blocker Recalls

    www.ahajournals.org/doi/10.1161/HYPERTENSIONAHA.119.13955

    Since July 2018, >2 dozen specific ARB products have been recalled owing to the presence of potentially carcinogenic nitrosamine impurities in selected lots. As is the case with all U.S. drug recalls, the ARB recalls have been voluntary on the part of the companies involved.

  10. Valsartan recall: 4 things patients should know - CNN

    www.cnn.com/2018/07/19/health/valsartan-recall-explainer

    Several common drugs that contain valsartan, used to treat high blood pressure and heart failure, have been recalled in the United States due to an “impurity” in the drug that poses a potential...

  11. Valsartan: FDA Recall Announcement, Side Effects & Shortage

    www.consumernotice.org/drugs-and-devices/valsartan

    In July 2018, the U.S. Food and Drug Administration announced that three companies had voluntarily recalled several lots of valsartan, which is the generic version of Diovan, because they were contaminated with N-nitrosodimethylamine, or NDMA.