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drug_recall zelnormIn 2002, the U.S. Food and Drug Administration approved the drug Zelnorm for the treatment of constipation and irritable bowel syndrome despite existing safety concerns. Five years later, drug manufacturer Novartis AG halted all sales and distribution of the drug after a report linked Zelnorm to serious cardiovascular side effects and risks including heart attack and stroke. Unfortunately, over 500,000 Americans have been prescribed the drug since it's release.
If you or a loved one has suffered harm as a result of serious Zelnorm side effects , it is important to consult with a proven and experienced defective drug lawyer who can inform you of your legal rights and options. You may be entitled to recover your damages. Please contact us today to schedule a FREE case evaluation with an experienced attorney near you.
What You Should Know About Zelnorm
Zelnorm's withdrawal from the U.S. market followed the results of a data analysis involving more than 18,000 patients taking the drug. The study shows that .11 percent of Zelnorm patients experienced some type of serious cardiovascular effect compared to .01 percent of participants who took a placebo. One of the 13 patients who suffered an adverse event associated with the use of the drug died.
Side effects linked to Zelnorm include:
• Stroke
• Heart attack
• Angina
• Death
Individuals who experience any of these cardiovascular effects are urged to get medical help and report all adverse events to the FDA.
Zelnorm and Your Legal Rights
If you or a loved one has suffered serious injury or death as a result of taking Zelnorm, you may be eligible to seek compensation for your losses including medical bills, pain and mental anguish, lost income capacity, and more. Please contact us today to get in touch with a qualified and caring product liability attorney who can evaluate your case at no cost, protect your legal rights and interests, and help you get the compensation and justice you deserve.