Another manufacturer has issued recalls for Irbesartan after the frequently prescribed blood-pressure medication tested positive for a probable human carcinogen.
A detailed article examining the latest in a series of recalls is available here.
According to the United States Food and Drug Administration (FDA), a pharmaceutical manufacturer has recalled multiple lots of Irbesartan. These drugs, classified as angiotensin receptor blockers (ARBs), are commonly prescribed to treat high blood pressure and congestive heart failure.
About the Latest Recalls
Prinston Pharmaceuticals has recalled eight lots of Irbesartan and Irbesartan/Hydrochlorothiazide (HCTZ) tablets after those drugs tested positive for trace amounts of N-nitroso-diethylamine (NDEA), which is a probable human carcinogen. According to additional sources, the recalled products include:
Patients who take these medications are advised to check with a qualified physician before discontinuing any medications. Additional information on these recalls is available at the FDA’s consumer-protection website.
More of the Same
As we reported in an earlier blog, medications containing the active ingredient Valsartan—a product similar in class and formulation to both Irbesartan and Losartan—have recently been recalled over similar contamination issues. Those recalls involved Major Pharmaceuticals, Solco Healthcare, Teva Pharmaceuticals, and Mylan Pharmaceuticals.
Graves McLain is Here to Help
If you or a loved one has been injured by a —including Valsartan, Losartan, or Irbesartan—call Graves McLain right away at 918-359-6600 or fill out a free consultation form online. When you call, one of our experienced Tulsa, Oklahoma Dangerous Drug Attorneys will speak with you for FREE—and determine the best course of action.
We review every detail of your situation at no cost to you—and fight hard to protect your rights.
Trust our team, we are here to help.
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