Over the past several months, you may have heard that the FDA has recalled certain lots of angiotensin II receptor blocker (ARB) medications due to the presence of impurities. These contaminants — nitrosamine impurities — may occur as a byproduct of the manufacturing process. They include N-Nitrosodiethylamine (NDEA) and N-Nitrosodimethylamine (NDMA), which can potentially cause cancer. These substances are found in the environment as well in meats, dairy products, and water, but their presence in medications is not acceptable. Therefore, the FDA sets acceptable safety limits on the presence of these impurities in drugs. Which blood pressure medications are affected? ARBs have been in use since the 1990s and are still widely used today. They effectively lower blood pressure, and also reduce deaths and complications
from http://besthealthnews.com/2019/08/what-should-you-do-if-your-blood-pressure-medication-has-been-recalled/?utm_source=rss&utm_medium=rss&utm_campaign=what-should-you-do-if-your-blood-pressure-medication-has-been-recalled
from
https://healthnews010.tumblr.com/post/186808552638
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