losartan potassium recall depakote

Losartan Potassium / Hydrochlorothiazide, USP 50mg/12.5mg, 90 count, batch No. "The risk of harm to the patient's health may be higher if the treatment is stopped immediately without any alternative treatment," federal health officials wrote in a statement.The FDA has said the contaminants likely resulted from a manufacturing change adopted by factories in China and India that make the drug ingredients. Patients should contact their pharmacist or physician who can advise them about an alternative treatment prior to returning their medication.Patients who are on losartan potassium and hydrocholothiazide tablets, USP should continue taking their medication, as the risk of harm to the patient's health may be higher if the treatment is stopped immediately without any alternative treatment.The products subject to recall are listed below and packaged in bottles. This recall was prompted due to the detection of trace amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA) a possible process impurity or contaminant in … Summary: Drug interactions are reported only by a few people who take Depakote and Losartan potassium and … However, not all ARBs have been affected, and patients should continue to use their medication, the FDA says. The recall is due to … Losartan potassium is available as tablets for oral administration containing either 25 mg, 50 mg or 100 mg of losartan potassium and the following inactive ingredients: colloidal silicon dioxide, hydroxypropyl cellulose, hypromellose, lactose anhydrous, magnesium stearate, microcrystalline cellulose, pregelatinized starch, talc and titanium dioxide. Torrent Pharmaceuticals Limited is expanding its voluntary recall from 10 lots of Losartan potassium tablets USP to include 6 lots of Losartan potassium and … The product can be identified by checking the product name, manufacturer details and batch or lot number on the bottle containing these products.Losartan potassium tablets, USP were distributed nationwide to Torrent’s wholesale distributor, repackager and retail customers.Consumers with medical questions regarding this recall or to report an adverse event can contact Torrent Pharmaceuticals Limited at:Consumers should also contact their physician or healthcareAny general questions regarding the return of this product should be directed to Qualanex at 1-888-280-2040 (live calls received 8 am - 9:00 pm Eastern Time).Adverse reactions or quality problems associated with the use of this product may be reported to FDA's MedWatch Adverse Event Reporting program either by phone, on line, by regular mail or by fax.This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. You can find out drug interactions, minor or serious, reported by people like you. Each losartan potassium tablet, USP intended for oral administration contains 25 mg or 50 mg or 100 mg of losartan potassium. 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.

© 2020 USA TODAY, a division of Gannett Satellite Information Network, LLC. Losartan potassium tablets, USP; Losartan potassium and Hydrochlorothiazide tablets, USP An official website of the United States government: In addition, each tablet contains the following inactive ingredients: colloidal silica anhydrous, hydroxypropyl cellulose (low substituted), hypromellose, lactose monohydrate, magnesium stearate, maize starch (corn starch), …

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