Abstract
The abuse of ipecac syrup for three years resulted in painless, nonfatigable, chiefly proximal weakness in a 27-year-old woman. Electromyography (EMG) and a muscle biopsy revealed features of a myopathy similar to those previously reported in experimental emetine myopathy. Clinical weakness and EMG abnormalities improved after discontinuation of ipecac administration. A direct toxic action of ipecac (acting through its active alkaloid, emetine hydrochloride) on muscle fibers seemed to be responsible for the weakness in this patient. © 1985, American Medical Association. All rights reserved.
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CITATION STYLE
Mateer, J. E., Farrell, B. J., Chou, S. S. M., & Gutmann, L. (1985). Reversible Ipecac Myopathy. Archives of Neurology, 42(2), 188–190. https://doi.org/10.1001/archneur.1985.04060020106024
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