Zelnorm Attorney
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Ennis & Ennis, P.A. is representing individuals that have been harmed as a result of Zelnorm side effects. If you or a loved one have suffered from severe chest pain, heart attack or stroke as a result of Zelnorm use you may be entitled to compensation. Click here to contact one of our Zelnorm Attorneys about a Zelnorm lawsuit today.

Novartis will offer restricted Zelnorm for emergencies only

04/05/2008-
Having restricted its use last year, Novartis has now served notice that it intends to take its irritable bowel syndrome off the US market completely.

The Swiss drugs giant has notified the US Food and Drug Administration that it will no longer provide Zelnorm (tegaserod maleate) as part of a restricted programme agreed with the agency in July last year. That agreement saw Novartis provide the drug to treat IBS with constipation and chronic idiopathic constipation in women younger than 55 who meet certain conditions.

However, the product was being treated as an investigational new drug and patients needed to meet strict criteria and have no known or pre-existing heart problems. Zelnorm, known elsewhere as Zelmac, had been off the US market for general use since March 2007 when Novartis suspended sales because a safety analysis found a higher chance of heart attack, stroke, and unstable angina in patients treated with Zelnorm compared with placebo.

Now the FDA reports that Novartis will only supply Zelnorm for use in emergency situations only and requests for the drug must be made to the agency which in turn would authorise shipment from the manufacturer. An emergency situation is defined as one that is “immediately life-threatening or serious enough to qualify for hospitalisation”.

However the FDA may still deny authorisation “if exposure to Zelnorm would pose an unreasonable or a significant additional risk to patients”. Conditions to stop the drug being prescribed include a history of heart problems, diabetes, smoking, obesity, and depression, and Zelnorm could also be denied to people aged over 55.

The loss of Zelnorm last year was a major blow for Novartis as the drug brought in $561 million in 2006, though first-half 2007 sales fell 66% to $91 million as the effect of the suspension kicked in. The company has not revealed why it has completely pulled the plug on the treatment.


If you or a loved one have experienced Zelnorm side effects such as severe chest pain, heart attack, or stroke you may be entitled to compensation. Contact the Zelnorm attorneys of Ennis & Ennis today for a free confidential case evaluation. Our on staff nurse and attorneys are standing by to answer any questions you may have regarding Zelnorm side effects, a possible Zelnorm class action lawsuit, or any other type of Zelnorm litigation.

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