FDA Consumer Safety Officer Armando Zamora explains what to do if you think you may have a recalled product. He is dealing with a recurrence. The latest recall was this expansion to 40 repacked lots. Teva expanded this recall on June 10, 2019, with another six lots of losartan potassium USP tablets in 50mg and 100mg strength. RECALL: Losartan recalled again 1 year ago eExtra News . WebMD does not provide medical advice, diagnosis or treatment. In September, Torrent announced that an additional three lots of losartan potassium tablets in 100 mg and 50 mg doses, and two lots of losartan potassium/hydrochlorothiazide tablets 50 mg/12.5 mg, and 100 mg/25 mg are being recalled as well. The Schmidt Firm, PLLC is currently accepting Losartan induced injury cases in all 50 states. What do I do if I think I have recalled losartan? In the UK, where nearly half a million prescriptions for valsartan were issued in 2017, Dexcel Pharma and Accord-UK (formerly called Actavis UK) products have been recalled. The recall involves irbersartan and irbersartan HCTZ tablets manufactured in China. 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. 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. 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 agency has also created a page that lists the drugs that have not been recalled. Torrent Pharmaceuticals Ltd. has expanded its recall of losartan potassium and losartan potassium/hydrochlorothiazide tablets. Note: This story was updated on Sept. 23, 2019, with an additional losartan recall from Torrent Pharmaceuticals. I was on the brand name Toprol XL for about 5 years and never had a problem.-200mg. These common prescription drugs include valsartan, losartan, and irbesartan in different combinations and from different manufacturers. For context, 1 in 3 people in the United States will be diagnosed with cancer in their lifetime. In July, the FDA announced a voluntary recall of irbesartan tablets. An FDA spokesman says the agency is still investigating how these drugs became contaminated. This is the third type of impurity to cause recalls of these medications. The amount of NDMA found in the recalled valsartan drugs exceeds acceptable levels. Torrent Pharmaceuticals Limited is expanding its recall for Losartan Potassium Tablets USP and Losartan Potassium/hydrochlorothiazide tablets, USP, to the consumer level due to the detection of trace amounts of an unexpected impurity while testing the below finished product batches … See all the affected products here. Consumers should not stop taking their medication without an alternative or replacement from their pharmacist or doctor, the agency said. 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. Virtually every day, the federal government announces that a product has been recalled. The pills come in 100-count blister packs with NDC number 60687-139-01. If you experience negative side effects while taking this drug, a number of other medications are available that work differently than Losartan. Losartan was recalled due to impurities found while testing finished products. 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. The recalled lots of Losartan were manufactured by Zhejiang Huahai Pharmaceutical Co. Ltd., the same company that manufactured the NDMA -contaminated Valsartan. Almost 60 million prescriptions were written for losartan drugs in 2016 and 14 million for valsartan or a drug that includes it. The drug company Sandoz has recalled the Losartan lot because of a potential contamination with the impurity NDEA from its manufacturing facility in China. All three are classified as a probable human … Camber Pharmaceuticals on Feb. 28 recalled 87 lots of losartan tablets USP 25mg, 50 mg and 100 mg. See the affected products and what the label looks like. Legacy Pharmaceutical Packaging, LLC on March 15 recalled 43 lots of losartan tablets. This allows you to instantly identify a product that might have a problem. If that information is not on the bottle, contact the pharmacy that dispensed it to you. Here's what the experts say you should know — and do — if a drug you take has been recalled or pulled from drugstore shelves. Yet another blood pressure drug has been recalled because of fears of impurities added by a lab in China. Doctors prescribe losartan for patients with high blood pressure and for Type 2 diabetics who have nephropathy. If you buy a can of tomatoes or infant formula, you will find a Lot Number and a Use By/Expiration Date. Macleods on June 26 also recalled 32 lots of losartan potassium including two lots of 50 mg tablets and losartan potassium/hydrochlorothiazide tablets, including 12 lots of 50 mg/12.5 mg strength, three lots of 100 mg/12.5 mg and 15 lots of 100 mg/25 mg strength. NDEA is used to make rocket fuel and can also be found in some food and drinking water, but at low levels. But with lower costs sometimes comes lower quality control. © 2021 USA TODAY, a division of Gannett Satellite Information Network, LLC. *. Golden State re-packages the tablets under its own label for retail sale. What blood pressure drugs have been recalled? Losartan is a type of blood pressure medication that works by blocking receptors for angiotensin, an enzyme that can cause blood pressure to increase. 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. Macleods Pharmaceuticals Limited on Feb. 25 recalled one lot of losartan potassium/hydrochlorothiazide combination tablets 100mg/25mg, with a July 2019 expiration date. Here’s what to watch out for. 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. The FDA says it is very small. There have been so many types of valsartan recalled this year that the FDA has created a website listing just for them. Then my new coverage was not covering so doctor switched me to Coreg CR-80mg- it seemed to work, although BP was a little elevated. Ryan W. Miller. The drugs were made in India and distributed by Heritage Pharmaceuticals of East Brunswick, NJ. 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. The Public Interest Research Group said in March that the FDA needs to step up the pace. Yet another blood pressure drug has been recalled because of fears of impurities added by a lab in China. "After 75 recalls it is clear more aggressive action is needed," PIRG consumer watchdog Adam Garber said in a release. The latest is American Health Packaging's 160 mg valsartan tablets, lot number 179791 that expire on March 31, 2020. Similar to NDMA, the chemical could possibly cause cancer. I have some of the recalled Losartan; what do I do now? See which products were affected by the recall. Clicking the “Medicine” tab will lead you to the FDA page on the site, from which you can go on to http://www.fda.gov/Safety/Recalls/ (which you can also access directly). Explore >>Read: Recall alert: 80 lots of Valsartan blood pressure tablets recalled. To find out whether your medication is under recall, check the FDA website for all three drugs. Numerous blood pressure medications in recent months have been recalled over concerns of possibly carcinogenic ingredients. The … No rebound effect on withdrawal of losartan has been noted. But at least one expert says the recalls are making it more difficult to find valsartan drugs that have not been recalled. Losartan potassium hydrochlorothiazide (Losartan) was also recalled by Sandoz Inc. in November over cancer concerns due to an impurity impurity N-nitrosodiethylamine, according to … See the affected products and what the label looks like. The FDA needs to finish its investigation and develop a plan to prevent further contamination.". Your doctor or pharmacist can help you find an alternative. The original recall of valsartan was issued because batches were discovered to have been contaminated by a substance believed to cause cancer. See which products were affected by the recall. Numerous blood pressure medications in recent months have been recalled over concerns of possibly carcinogenic ingredients. Follow USA TODAY's Ryan Miller on Twitter: @RyanW_Miller. In April, the agency  released a list of 40 blood pressure medications it says are free from contamination. Supermarkets scan products during check out. (I was also on Cozaar and then Avapro). Keep taking your medication. It can also be created through certain chemical reactions and as a byproduct of industrial processes. In January 2019, Prinston Pharmaceutical Inc., doing business as Solco Healthcare LLC, voluntarily recalled eight lots of irbersartan-based drugs. The amount of NDMA found in the recalled valsartan drugs exceeds acceptable levels. The FDA released a list of all the contaminated blood pressure medications. When American Health Packaging recalled one lot of valsartan pills on March 7, the Public Interest Research Group said it was the 75th recall of blood pressure medications since the problem first appeared. NDMA and NDEA are probable carcinogens, and the FDA has found levels of the impurities in three drugs: valsartan, irbesartan and losartan-containing products, the agency says. See a list of affected products here and here. Nearly 8 out of 10 active pharmaceutical ingredients, which are made into pills at other plants, are, too. You can find the list here. 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. This globalization of the nation’s drug supply helps keep prices down, as it is cheaper to have them made in other countries. The threat from the contamination may be less than the threat of not taking the drug. On April 24, the company recalled an additional lot of 50mg losartan tablets. USA TODAY. More blood pressure medicines recalled over possible cancer-causing impurity . I don't know if I spelled any of that correctly. This article was last updated on 04 April, 2019 The impurity, known as NDEA, was found in the drug’s key ingredient made by Zhejiang Huahai Pharmaceutical Co. in China. Torrent further expanded the recall in April for 36 more lots of losartan potassium tablets and 68 lots of losartan potassium/hydrochlorothiazide tablets. The impurity found in these batches is N-Methylnitrosobutyric acid (NMBA). Dozens of blood pressure medications have been recalled since the first products were pulled off the shelf in July 2018 due to impurities. Let friends in your social network know what you are reading about. The FDA has traced the recalled drugs to Chinese manufacturers Zhejiang Huahais and Zhejiang Tianyu as well as Hetero Labs Limited in India. Not all ARBs contain NDMA or NDEA or are under recall, the FDA says. On May 4, Vivimed Life Sciences Pvt Ltd recalled 19 lots of losartan potassium tablets in 25 mg, 50 mg and 100 mg doses. 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). 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.". See the full list here. Then, check to see if the manufacturer is listed on the bottle. A link has been posted to your Facebook feed. 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