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The FDA says it has recalled 580,000 bottles of blood pressure medication due to cancer risks.

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The Federal Drug Administration (FDA) says pharmaceutical companies have recalled more than 580,000 bottles of blood pressure medication over concerns they may contain chemicals that cause cancer.

A national voluntary issue issued by New Jersey-based pharmaceutical company Teva Pharmaceuticals USA and drug distributor Amerisource Health Services. reminisce More than 500,000 bottles of Prazosin capsules in various strengths were sold earlier this month, according to the FDA.

The capsule drug known as prazosin hydrochloride is available in 1 mg, 2 mg, and 5 mg dosages. It helps relax blood vessels and promote blood flow, and is sometimes prescribed for nightmares and other sleep disorders caused by post-traumatic stress disorder.

Teva Pharmaceuticals did not immediately respond to a request for comment.

In recall command According to a posting on its website, the FDA said it classified the affected recalled drugs as a level 2 hazard because some of the recalled drugs may have the following risks: Nitrosamines Impurities considered potentially carcinogenic. The chemicals can form when the drug is manufactured or stored, the FDA said.



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