Blood pressure medicine recalled over high levels of cancer-causing

Blood pressure medicine recalled over high levels of cancer-causing

More than half one million bottles of blood pressure medication have been recalled over high levels of a chemical compound that may trigger cancer, the Food and Drug Administration said.

Parsippany, NJ-based Teva Pharmaceuticals USA recalled 580,844 bottles of Prazosin Hydrochloride earlier this month.

The medication is an alpha blocker taken to decrease high blood pressure.

More than half one million bottles of blood pressure medication have been recalled. Teva Pharmaceuticals

Testing revealed high levels of “N-nitroso Prazosin impurity C” in the drug, the FDA said. Teva Pharmaceuticals

Testing revealed high levels of “N-nitroso Prazosin impurity C” in the drug, the FDA said last week.

The chemical’s focus was so high that it surpassed the FDA’s security limits for its potential to trigger cancer.

Different variations of the drug – including 1 mg, 2 mg and 5 mg doses – have been included in the recall affecting bottles with anyplace from 100 to 1,000 capsules.

The FDA not too long ago categorised the recall as Class II, which is the second-highest of three threat levels.

A Class II label signifies that use of the medication “may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote,” according to the company.

As of Thursday morning, the drugmaker apparently had not offered directions on whether or not customers ought to toss or flip in bottles of the recalled product.

Teva Pharmaceuticals USA didn’t instantly reply to The Post’s request for remark.

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