Propulsid To Go Off Market - Warning
This warning is based on a press release from the U.S. Food and Drug Administration (July 14, 2000). It is meant to alert people who are currently taking Propulsid (cisapride) that it is going to be removed from the market in July. For some more key information about this drug, please visit our Propulsid (cisapride) Center.
-- Medical Editor, MedicineNet.com
Janssen Pharmaceutica Inc., of Titusville, N.J., has announced that it has decided to stop marketing cisapride (Propulsid) in the United States as of July 14, 2000. The effective date of the voluntary action is intended to provide adequate time for patients and physicians to make alternative treatment decisions.
Cisapride is a prescription drug treatment approved only for severe nighttime heartburn experienced by adult patients with gastroesophageal reflux disease (GERD) that does not adequately respond to other therapies.
As of December 31, 1999, use of cisapride has been associated with 341 reports of heart rhythm abnormalities including 80 reports of deaths. Most of these adverse events occurred in patients who were taking other medications or suffering from underlying conditions known to increase risk of cardiac arrhythmia associated with cisapride.
Patients who are currently prescribed cisapride are urged to promptly contact their health care providers to discuss alternative treatments.
Physicians who are treating patients with severely debilitating
conditions for whom they believe the benefits of the cisapride may
still outweigh its risks are encouraged to contact Janssen at 1-800-
JANSSEN. The company will continue to make the drug available to
patients who meet specific clinical eligibility criteria for a
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