ZELNORM – In March 2007, Novartis AG (NYSE: NVS), the make of Zelnorm, voluntarily withdrew the drug from the market after strong pressure from the FDA.  FDA advisories reported that patients who had been prescribed Zelnorm (a.k.a. Zelmac) to treat Irritable Bowel Syndrome (IBS) experienced heart problems and heart attacks. 

However, Zelnorm did return to the market with tighter restrictions and stricter warnings.

If you were prescribed or are prescribed Zelnorm or Zelmac and you experience chest pain, shortness of breath, dizziness, weakness, difficulty walking or talking, or other symptoms associated with a heart attack or stroke, it is likely that Zelnorm is or was the reason for the problems.  You or your loved one may be entitled to compensation if Zelnorm is found to be the reason for the complications.

Unsafe drug cases are complex and costly to litigate.  Experienced representation is essential, and that is exactly what we help provide.  If you believe you or a loved one suffered a serious complication as a result of taking Zelnorm, please fill out the form below for a free evaluation.
 
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