Urinary excretion kinetics of intact quinidine and 3-OH-quinidine after oral administration of a single oral dose of quinidine gluconate in the fasting and non-fasting state

Author:

St-Onge Jean-Maurice,Sirois Gerard,Gagnon Marc-Andre

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology

Reference30 articles.

1. Ochs H.R., Greenblatt D.J. and Woo E. (1980): Clinical pharmacokinetics of quinidine. Clin. Pharmacokinet.,5, 150–168.

2. Soeterboek A.M. (1980): The serum concentrations of drugs. Section: Quinidine: analytical, biopharmaceutical and pharmacokinetic aspects, ed. by F.W.H.M. Merkus, pp. 180–192, Excerpta Medica, Amsterdam.

3. Huynh Ngoc T., Chabot M. and Sirois G. (1978): Biovailability of three commercial sustained-release tablets of quinidine in maintenance therapy. J. Pharm. Sei.,67, 1456–59.

4. Koch-Weser J. (1973): Proc. 5 th international congress of pharmacology, San Francisco, 1972. Vol. 3: Correlation of serum concentrations and pharmacologic effects of antiarrhythmic drugs, ed. G.H. Acheson, pp. 69–85, S. Karger AG, Basel.

5. Fieldman A., Beebe R.D. and Chow M.S.S. (1977): The effect of quinidine sulfate on QRS duration and QT and systolic time intervals in man. J. Clin. Pharmacol.,17, 134–139.

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