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There are so many now that the administration created a tool to help consumersВ figure out if they have been exposed to potentially toxic medications. The FDA has had to expand its list of tablets affected by the unsafe levels of NDMA more than a dozen times to include additional batches that are unsafe for human consumption. However, several companies have had to recall many medication batches, and there are thousands of patients who took contaminated Losartan before the FDA findings. Even after the FDA published the guide, several companies, both named and unnamed in the Losartan lawsuits, have voluntarily recalled their versions of the drug. The FDA created a guideВ to help drug producers develop products that are safe for consumers. Or, they knew the pills contained the probable carcinogens and failed to notify the public or the FDA. However, the pharma labs with high contamination levels did not have proper quality control measures in place to test the drugs. When pharmaceutical companies manufacture the drug correctly, very little of the potentially carcinogenic compounds result from the process. The toxic chemicals are a by-product of the manufacturing process. The products recalled held dangerous levels of MNBA, which has a similar threshold to another cancer-causing compound, Nitrosodimethylamine (NDMA).Д«oth MNBA and NDMA are in the generic drugs, and the FDA does not oppose low levels of these two chemicals in Losartan. Upon notice from the FDA, many of the makers voluntarily recalled their products. The Food and Drug Administration notified several companies that the generic Losartan they were producing contained impurities that made them unsafe for human consumption. So, the potential risks if you were taking the tainted prescription are substantial. These drugs treat life-threatening cardiovascular conditions. In addition to exposing users to several probable human carcinogens, the medication was not an effective treatment. NDMA levels in some pills were 20 times or more than the safe level of daily consumption for humans.

People who consume these toxins are at higher risk of developing bladder cancer and other potentially harmful side effects, including: Theses chemicals are known animal carcinogens and listed with the EPA as probable human carcinogens. Individuals who took Losartan for the treatment of hypertension, congestive heart failure, diabetic kidney damage, left ventricle enlargement, and other medical reasons may have been exposed to the cancer-causing chemicals N-Methylnitrosobutyric acid (NMBA), N-Nitrosodimethylamine (NDEA), and N-Nitrosodimethylamine (NDMA). So, these medications are a top choice by doctors treating people with diabetes and hypertension or kidney disease.

ARBs are especially useful for treating diabetic kidney disease, too. With the vessels wider and more relaxed, the patient should have lower blood pressure, and the heart should not have to work as hard to pump blood throughout the body. These drugs work by blocking the angiotensin II receptor, which creates an enzyme that restricts the blood vessels. It belongs to the family of angiotensin II receptor antagonists (ARB), which includes Valsartan and Irbesartan. Losartan is the generic form of Cozaar, a popular hypertension drug.

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If you were exposed but have not been diagnosed with cancer or another medical condition related to the drug, you may still be entitled to free cancer screenings, which could save your life if you do get cancer. If you or a family member took Losartan or a related drug and developed cancer, you may be entitled to a drug manufacturer settlement. Many people counted on these drugs to keep them healthy after suffering a stroke or heart attack or lower their high blood pressure to prevent a major heart event.В Unfortunately, patients taking the popular medication were left vulnerable to the very conditions the drugs claimed to treat and exposed to additional threats. The FDA found that more than a dozen manufacturers produced prescription drugs with unsafe levels of several probable human carcinogens. Doctors regularly prescribed antihypertensive drugs like Losartan, Valsartan, and Irbesartan to millions of patients in the United States and worldwide. Patients prescribed angiotensin II receptor medications have filed Losartan recall lawsuits against drug manufacturers.