Kansas City Zelnorm Injury Lawsuit Attorneys
Missouri • Kansas • Southern Illinois
The FDA has released a Public Health Advisory warning of "serious side effects" including heart attack and stroke. The medication has been withdrawn.
Zelnorm (tegaserod maleate), a widely prescribed medication for constipation was pulled off the market after studies showed that it is linked to serious ailments.
The drug, manufactured by Novartis and marketed for constipation or irritable bowel syndrome, was voluntarily pulled off the market after it was linked to heart attacked and strokes, according to federal regulators. An analysis of 29 studies involving more than 18,000 patients found that those who took the medication had significantly higher rates of cardiac problems than those who were given a placebo.
Patients who took or are taking Zelnorm should contact their healthcare professional to discuss treatment alternatives. You should seek emergency care if you experience:
- Severe chest pain
- Shortness of breath
- Sudden onset of weakness
- Difficulty walking or talking
- Other symptoms of a heart attack or stroke
For some patients, Zelnorm is a 'one of a kind' drug, with no substitute. There may be patients for whom no other treatment options are available and in whom the benefits of Zelnorm treatment outweigh the chance of serious side effects. FDA will work with Novartis to allow access to Zelnorm for those patients through a special program.
Contact the Attorneys at Brown & Crouppen
Contact a lawyer at our firm if you have taken Zelnorm and have suffered any serious side effects. Brown & Crouppen can help you make informed decisions about your legal rights, so please call Brown & Crouppen toll-free at 888-842-7944 for your free legal consultation or save time with our online contact form.
