Torrent Pharmaceuticals Ltd. has expanded its recall of losartan potassium and losartan potassium/hydrochlorothiazide tablets. See which products were affected by the recall. Keep taking your medication. For more information on the recalls, read all of USA TODAY's coverage here: Jan. 23: Blood pressure medication recall over cancer risk expanded for more losartan drugs, Jan. 18: FDA: Another blood pressure drug, irbesartan, recalled over cancer-causing impurity, Jan. 14: Blood pressure drug recall: FDA investigates foreign plants that made drugs with cancer-causing impurities, Jan. 7: More blood pressure medication recalled over carcinogen concerns — this time, losartan, Jan. 2: More blood pressure medication recalled: Company recalls 80 lots of valsartan over cancer concerns, Dec. 6: Three more blood pressure drugs recalled over cancer concern: Here's what you need to know, Nov. 30: Doctors: Blood pressure drug substitutes are available for patients affected by recalls, Nov. 30: Two more blood pressure drugs recalled for potential cancer risk, Nov. 14: FDA chief: Blood pressure medicine recalls reflect increased scrutiny on drug safety, Nov. 13: FDA recalls another blood pressure drug for possible cancer risk, Nov. 2: Blood pressure drug recalled for possible cancer risk, FDA says, Aug. 7: FDA expands recall of heart drug for possible cancer-causing contamination, Contributing: Ken Alltucker, USA TODAY. Company: Medicine: National Drug Code (NDC) Lot Number: Expiration: A-S Medication … He is dealing with a recurrence. Torrent's recall was expanded on Jan. 22 to include 10 additional lots of losartan potassium tablets, and six lots of losartan potassium and hydrochlorothiazide tablets. We've compiled the recalled valsartan medications in the expandable table below: Valsartan Recall List Expand to See a Full List of Recalled Valsartan. Yet another blood pressure drug has been recalled because of fears of impurities added by a lab in China. Ryan W. Miller. To find out whether your medication is under recall, check the FDA website for all three drugs. These are not yet listed on the FDA's website of all recalled ibersartan products. These alternatives still decrease blood pressure, but do not block the angiotensin … I never had a problem until this new doctor switched me to generics in October of … In December, the FDA announced a voluntary recall of losartan potassium tablets USP. This is the third type of impurity to cause recalls of these medications. Craig Beavers, PharmD, cardiovascular clinical pharmacy coordinator, University of Kentucky Medical Center. The impurity found in these batches is N-Methylnitrosobutyric acid (NMBA). Losartan was recalled due to impurities found while testing finished products. *. If a can of beans is recalled, someone can contact you to bring them back for a refund. For context, 1 in 3 people in the United States will be diagnosed with cancer in their lifetime. Drug Recalls: Why They Happen and What You Should Do, Medication Safety: Side Effects, Medication Disposal, Expiration Dates, and More, Blood Pressure Often Differs Widely Between Arms, High BP in Middle Age Can Harm Your Brain, Untreated High Blood Pressure a Growing Problem, Remote Monitoring May Help Control High Blood Pressure, Blood Pressure Meds Don't Raise Risk of Depression, Young Black Americans at High Risk of Hypertension. An additional 3.6 million prescriptions were written for irbesartan that year. The media reports on bigger recalls, like the recent one involving General Motors, but most are under the radar, says Ed Mierzwinski, the consumer program director of the U.S. Public Interest Research Group. The other two are N-Nitrosodimethylamine (NDMA) and N-Nitrosodiethylamine (NDEA). So he also has tachycardia, very very low blood pressure, and partial gastroparesis. On the home screen, you will find a list of tabs along the top. Nearly 8 out of 10 active pharmaceutical ingredients, which are made into pills at other plants, are, too. Robert Handfield, director of Supply Chain Resource Cooperative, North Carolina State University. What should people who rely on these medicines do? Records from drug manufacturers show the impurity may have been in the valsartan products for up to 4 years. The latest recall was this expansion to 40 repacked lots. © 2021 USA TODAY, a division of Gannett Satellite Information Network, LLC. The FDA says it is very small. The FDA says it is very small. In April, the agency  released a list of 40 blood pressure medications it says are free from contamination. In September 2018, the FDA announced it had found another toxic chemical in tainted valsartan batches called N-nitrosodiethylamine (NDEA). The Public Interest Research Group said in March that the FDA needs to step up the pace. My husband has stage IV non small cell lung cancer. Virtually every day, the federal government announces that a product has been recalled. The FDA has traced the recalled drugs to Chinese manufacturers Zhejiang Huahais and Zhejiang Tianyu as well as Hetero Labs Limited in India. See all the affected products here. With the exception of neonatal weight gain (which was affected at … The Food and Drug Administration posted information on its website listing the blood pressure medications recalled for containing carcinogens. There have been so many types of valsartan recalled this year that the FDA has created a website listing just for them. "Our goal is for this information to help health care providers as they consider acceptable treatment options for their patients," the agency said in a statement. Not every manufacturer is affected, nor every batch from those that are. And that’s troubling because “recalls can be a matter of life and … And, they say, some blood pressure drugs not on the recall list have seen price increases as demand spikes. The drugs were made in India and distributed by Heritage Pharmaceuticals of East Brunswick, NJ. It can also be created through certain chemical reactions and as a byproduct of industrial processes. For valsartan-containing products currently recalled. These drugs work by widening or relaxing blood vessels, thus lowering blood pressure. The Schmidt Firm, PLLC is currently accepting Losartan induced injury cases in all 50 states. The impurity, known as NDEA, was found in the drug’s key ingredient made by Zhejiang Huahai Pharmaceutical Co. in China. But with lower costs sometimes comes lower quality control. Hello,I am Dr. Aren, I have over 38 years of clinical experience, I will help with your query.Since Losartan has been recalled,use of Irbesartan to replace these ARBs is recommended.Another alternative drug Amylodepine belongs to a different class ,but is as effective.These drugs are effective alternative for the drugs which have been recalled.Trials were done on this and the … Doctors prescribe losartan for patients with high blood pressure and for Type 2 diabetics who have nephropathy. This product is being recalled due to the trace amount of an impurity, N-nitrosodiethylamine (NDEA) contained in the API Losartan, USP manufactured by … Consumers should not stop taking their medication without an alternative or replacement from their pharmacist or doctor, the agency said. NDEA is thought to possibly cause cancer, according to the International Agency for Research on Cancer. Losartan. In each case, a recalled drug was contaminated with N-nitrosodimethylamine (NDMA), N-nitrosodiethylamine (NDEA) or N-Nitroso N-Methyl 4-amino butyric acid (NMBA). Your doctor or pharmacist can help you find an alternative. A widespread recall of common blood pressure and heart failure medications has been expanded to include more drugs containing losartan due to … In November, the FDA announced a voluntary recall of losartan potassium/hydrochlorothiazide, 100 mg/25 mg tablets in 1,000-count plastic bottles, NDC 0781-5207-10, Lot number JB8912, Exp. "After 75 recalls it is clear more aggressive action is needed," PIRG consumer watchdog Adam Garber said in a release. It left him with bilateral paralyzation of the vocal folds and a vagus nerve disorder. I was on the brand name Toprol XL for about 5 years and never had a problem.-200mg. How Do I Know if my Valsartan Has Been Recalled? A common thread among all of these recalls is that the drugs, or ingredients in the drugs, were all made in China or India. Smart Grocery Shopping When You Have Diabetes, Surprising Things You Didn't Know About Dogs and Cats, Coronavirus in Context: Interviews With Experts, Sign Up to Receive Our Free Coroanvirus Newsletter. It may take up to a week for significant blood pressure lowering or kidney effects are noted, with maximal effects occurring in 3 to 6 weeks. The pills come in 100-count blister packs with NDC number 60687-139-01. This allows you to instantly identify a product that might have a problem. USA TODAY. Golden State re-packages the tablets under its own label for retail sale. Numerous blood pressure medications in recent months have been recalled over concerns of possibly carcinogenic ingredients, leaving some consumers wondering how to tell whether their medicines are safe. You may get a call, letter or email from your pharmacy or your doctor's office if a prescription drug you take has been recalled. NDEA is found naturally in certain … These common prescription drugs include valsartan, losartan, and irbesartan in different combinations and from different manufacturers. Thosechemicals are believed to cause cancer in humans. WebMD does not provide medical advice, diagnosis or treatment. Teva expanded this recall on June 10, 2019, with another six lots of losartan potassium USP tablets in 50mg and 100mg strength. In previous reports the FDA has indicated that the level of risk to individual patients is very low, but it’s still high enough to warrant the recall. There are many numbers and dates … If you are taking any medication containing valsartan, losartan or irbesartan, compare the information on your prescription bottle with the information in this list (company, National Drug Code, lot number) to determine if your current medicine has been recalled. See the affected products and what the label looks like. Atlanta Journal-Constitution: “Blood pressure medication recalls: Everything you should know, Atlanta doctors, experts say.”, ClinCal.com: “Valsartan Drug Usage Statistics, United States, 2006 – 2016.”, Public Interest Research Group: "Blood pressure medication recalled for 75th time in 8 months.". Read or Share this story: https://www.usatoday.com/story/news/health/2019/01/16/blood-pressure-drug-recall-how-know-if-your-medication-recalled/2582924002/, Blood pressure medication recall over cancer risk expanded for more losartan drugs, FDA: Another blood pressure drug, irbesartan, recalled over cancer-causing impurity, Blood pressure drug recall: FDA investigates foreign plants that made drugs with cancer-causing impurities, More blood pressure medication recalled over carcinogen concerns — this time, losartan, More blood pressure medication recalled: Company recalls 80 lots of valsartan over cancer concerns, Three more blood pressure drugs recalled over cancer concern: Here's what you need to know, Doctors: Blood pressure drug substitutes are available for patients affected by recalls, Two more blood pressure drugs recalled for potential cancer risk, FDA chief: Blood pressure medicine recalls reflect increased scrutiny on drug safety, FDA recalls another blood pressure drug for possible cancer risk, Blood pressure drug recalled for possible cancer risk, FDA says, FDA expands recall of heart drug for possible cancer-causing contamination, Your California Privacy Rights/Privacy Policy. No rebound effect on withdrawal of losartan has been noted. For losartan-containing products currently recalled. An FDA spokesman says the agency is still investigating how these drugs became contaminated. The FDA is also working to determine what exactly has caused the impurities and what changes need to be made in the manufacturing process to prevent it. Losartan is a type of blood pressure medication that works by blocking receptors for angiotensin, an enzyme that can cause blood pressure to increase. The recall involves irbersartan and irbersartan HCTZ tablets manufactured in China. If you or somebody you know has been diagnosed with cancer or other severe side effects, you should contact our lawyers immediately for a free case consultation. The FDA estimates that if 8,000 people took the highest valsartan dose, which is 320 milligrams, from recalled batches every day for 4 years, there would likely only be one additional case of cancer over the life of those 8,000 people. 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