Famotidine neither affects action potential parameters nor inhibits human ether-a-go-go-related gene (hERG) K+ current
Author:
Affiliation:
1. Department of Pharmacology, Yamanashi Research Center of Clinical Pharmacology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi
Publisher
Japanese Society of Toxicology
Subject
Toxicology
Link
https://www.jstage.jst.go.jp/article/jts/34/5/34_5_563/_pdf
Reference10 articles.
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2. Endo, T., Katoh, T., Kiuchi, K., Katsuta, Y., Shimizu, S. and Takano, T. (2000): Famotidine and acquired long QT syndrome. Am. J. Med., 108, 438-439.
3. Howden, C.W. and Tytgat, G.N. (1996): The tolerability and safety profile of famotidine. Clin. Ther., 18, 36-54.
4. Katayama, Y., Tsuzaki, T., Abe, K., Tomizawa, S., Izumi, T. and Tsurubuchi, Y. (2005): The inter-cell-line reproducibility of hERG assay using the whole-cell patch-clamping. J. Pharmacol. Sci., 97 (Suppl), 236P.
5. Langtry, H.D., Grant, S.M. and Goa, K.L. (1989): Famotidine. An updated review of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in peptic ulcer disease and other allied diseases. Drugs, 38, 551-591.
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