Pharmacokinetics of (+)-, (-)- and (+/-)-verapamil after intravenous administration.
Author:
Publisher
Wiley
Subject
Pharmacology (medical),Pharmacology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2125.1984.tb02371.x/fullpdf
Reference22 articles.
1. Clinical pharmacokinetics of verapamil in patients with atrial fibrillation;Anderson;Eur. J. clin. Pharmac.,1982
2. Effects of verapamil on P-R-intervals in relation to verapamil plasma levels following single i.v. and oral administration and during chronic treatment;Eichelbaum;Klin. Wochenschr.,1980
3. Influence of meso-caval shunt surgery on verapamil kinetics, bioavailability and response;Eichelbaum;Br. J. clin. Pharmac.,1980
4. Superiority of stable isotope techniques in the assessment of the bioavailability of drugs undergoing extensive first-pass elimination. Studies of the relative bioavailability of verapamil tablets;Eichelbaum;Eur. J. clin. Pharmac.,1981a
5. Simultaneous determination of the intravenous and oral pharmacokinetic parameters of (±)-verapamil using stable isotope-labelled verapamil;Eichelbaum;Eur. J. clin. Pharmac.,1981b
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