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NEUROLOGY 1998;51:581-583
© 1998 American Academy of Neurology

Pregnancy outcome following first trimester exposure to sumatriptan

S. Shuhaiber, BSc, A. Pastuszak, MSc, B. Schick, RNC, D. Matsui, MD, G. Spivey, MS, J. Brochu and G. Koren, MD

From The Motherisk Program, Division of Clinical Pharmacology and Toxicology, Department of Pediatrics and Research Institute, The Hospital for Sick Children and the University of Toronto (Dr. Koren, and S. Shuhaiber and A. Pastuszak), Ontario; Pennsylvania Healthline (B. Schick), Philadelphia, PA; Fetal Risk Assessment Program, Children's Hospital of Western Ontario (Dr. Matsui), London, Ontario, Canada; and Connecticut Pregnancy Exposure Information Service, Division of Human Genetics University of Connecticut Health Center (G. Spivey and J. Brochu), Farmington, CT.

Address correspondence and reprint requests to Dr. Gideon Koren, Division of Clinical Pharmacology/Toxicology, The Hospital For Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada.

We prospectively compared pregnancy outcome after exposure to sumatriptan with that of disease-matched controls and nonteratogen controls. There were no differences in the rates of live births, spontaneous abortions, therapeutic abortions, or major birth defects among the three groups. This first prospective report suggests that the use of sumatriptan during organogenesis is not associated with an apparent increased risk of major birth defects.


Received December 3, 1997. Accepted in final form March 13, 1998.




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