The FDA asked companies to voluntarily recall ranitidine that contained levels of NDMA that exceed the maximum daily intake level. Some of the tests revealed levels of NDMA that exceed the reasonably safe daily intake limit. The FDA published the results of its ranitidine tests on November 1, 2019. The reasonably safe daily intake limit of NDMA is between 0.096 micrograms (.032 parts per million). FDA Continues Testing Ranitidine Medications for Cancer-CausingĪccording to the FDA, consuming small doses of ranitidine per day is considered “reasonably” safe for humans. Exposure to high doses of ranitidine for long periods increases the risk of developing cancer. It is an environmental contaminant that can be found in various food products and water. Studies have shown that NDMA is a probable carcinogen for humans.
What is NDMA and Why Should I Be Worried? In September 2019, Health Canada requested that companies stop distributing ranitidine products in Canada as it assessed the NDMA risk. Many prescription and over-the-counter versions of ranitidine were available. Multiple manufacturers rushed to create generic versions of Zantac. It was a common medication prescribed by physicians for the treatment of acid reflux, heartburn, and ulcers.Ī lower dose of Zantac became one of the most popular over-the-counter medications for heartburn and acid reflux. The medication is a histamine-2 (HD) blocker. Zantac (a common brand name for ranitidine) entered the market in 1981. 10 Call For Help With Your Zantac Injury Lawsuit.9 What Should You Do If You Are Taking or Have Taken Zantac?.8 Benefits of Filing a Zantac – Ranitidine Lawsuit.7 How Can Rosen Injury Lawyers Help Me?.6 Do Not Wait to File a Zantac or Ranitidine Claim.5 Recovering Compensation for Zantac Cancer Claims.4 Zantac Lawsuits Filed Throughout the United States.3 FDA Continues Testing Ranitidine Medications for Cancer-Causing.2 What is NDMA and Why Should I Be Worried?.
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