Another blood pressure medicine is being voluntarily recalled after tests showed it is tainted with a potential cancer-causing chemical.
The US Food and Drug Administration announced the recall for losartan potassium hydrochlorothiazide, made by the company Sandoz.
The active ingredient in the drug contains N-Nitrosodiethylamine (NDEA), a chemical “considered to be reasonably anticipated to be a human carcinogen."
It involves the 100 milligram/25 milligram tablets, but not other versions of the drug, sometimes sold under the brand names Hyzaar. The batch involves the lot number JB8912.
It’s important to note that most blood pressure medication has not been recalled. However, the FDA listed certain lots of Valsartan and Amlodopine as potentially contaminated and recalled as well. The Valsartan-containing pills have been under a recall since July. The drugs were tainted with NDEA or NDMA, N-nitrosodimethylamine, an impurity that is also considered a possible carcinogen. The FDA is currently testing all other related blood pressure medicines for impurities.
The FDA keeps a list of recalled blood pressure drugs non-recalled blood pressure drugs for consumers.
The risk of getting cancer from taking one of these medications is thought to be extremely low. The FDA asks patients to consult their doctors and replacing any medicine that has been recalled.
According to PubChem, NDEA is used in industry materials as an additive to gasoline and lubricant, as an antioxidant, and a stabiliser in plastics. When heated highly enough, it can emit toxic fumes.
NDMA is used to make liquid rocket fuel and is a byproduct of manufacturing some pesticides and processing fish.
