Video Siteaccident attorneys - car wrecks, motorcycle crashes, dog bites, workers compensation, defective products -  with lawyers in pittsburgh, altoona, ebensburg, erie, and johnstown1-866-9-4EDGAR or 1-866-943-3427
Bookmark and Share

Zencore Tabs Recalled for Undeclared ED Drugs

September 2007

Zencore Tabs recalled Zencore Tabs, a male enhancement dietary supplement, have been recalled due to hazardous ingredients. The Food and Drug Administration found that some Zencore Tabs contain undeclared prescription drugs used to treat Erectile Dysfunction (ED). That means Zencore Tabs carry the same potential risks as their ED prescription counterparts, only without the important package warnings.

It was revealed that one lot of Zencore Tabs contained a variant of tadalafil, the active ingredient in the ED drug Cialis. Notable side effects may include back pain, muscle aches, and other adverse symptoms. Also, the FDA discovered Cialis could lead to vision impairment in certain patients, especially in diabetics.

Another lot of Zencore Tabs was found to contain a variant of sildenafil, the active ingredient in prescription ED drugs such as Viagra and Revatio. Serious side effects of this drug include heart attack, priapism, stroke, and vision impairment. HIV patients are also at an enhanced risk for side effects when sildenafil is combined with Protease inhibitors.

Both sildenafil and tadalafil may react with nitrates, popular ingredients in drugs that treat blood pressure, cholesterol, diabetes, and heart disease. Combining these ED drugs with nitrates could result in a drastic drop in blood pressure to dangerously low levels.

Please note: All of our lawyers are licensed to practice in the state of Pennsylvania. We also have lawyers licensed to practice in Maryland, Ohio, and West Virginia, and we associate with experienced attorneys in other states. In addition, all drug-related litigation may involve co-counsel.

Source: "Bodee LLC, Inc. Issues A Voluntary Nationwide Recall of All Zencore Tabs, a Product Marketed as a Dietary Supplement." FDA Alert. August 31, 2007.