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From Rush University Medical Center (C.G.G.), Chicago, IL; and University of Rochester (S.R.S., S.W.E., D.O., I.S.), Rochester, NY.
Address correspondence and reprint requests to Dr. Christopher G. Goetz, Rush University Medical Center, Suite 755, 1725 West Harrison Street, Chicago, IL 60612; e-mail: cgoetz{at}rush.edu
The authors examined age effects on adverse events from two randomized, controlled trials of rasagiline, comparing younger (younger than70 years) and older (70 years and older) subjects. Older patients were more prone to serious adverse effects than younger patients, but there was no statistical interaction between age and rasagiline exposure. This absence of an age-rasagiline interaction suggests that rasagiline does not require special safety precautions for elderly subjects with Parkinson disease.
*The Parkinson Study Group investigators are listed in the appendix.
Disclosure: TEMPO and PRESTO studies were supported in the United States by Teva Neuroscience, Inc., in partnership with Eisai, Inc., and by TEVA Pharmaceutical Industries Ltd. and Lundbeck A/S. No additional funding was provided for the data analysis pertinent to this report.
Received July 12, 2005. Accepted in final form January 26, 2006.
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