Abstract
In the last few years the number of calcium antagonists available for treatment has increased rapidly since these drugs were shown to be effective in the treatment of stable and unstable angina pectoris. Gallopamil is a new calcium antagonist which appears to be three to four times more potent in animals than verapamil (3,4). About 90% of the dose of gallopamil is absorbed and its bioavailability is about 25% (21). Studies in patients give a mean half-life of 2.8 to 4.8 hours (21), with the concentrations of the unchanged substance peaking one to 2 hours after administration (20). After intravenous administration, this drug dilates the arteries and veins (5, 14), reduces peripheral arterial resistance and the work of the heart (−13%), and myocardial oxygen uptake (−10%), (12). It also dilates the epicardial coronary vessels and prevents vasospasm (10, 11): Gallopamil reduces sino-atrial node excitability and slows conduction in the AV node (4, 6).
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References
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© 1989 Dr. Dietrich Steinkopff Verlag GmbH & Co. KG, Darmstadt
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Scrutinio, D. et al. (1989). Treatment of chronic stable angina pectoris with gallopamil. In: Bender, F., Meesmann, W. (eds) Treatment with Gallopamil. Steinkopff. https://doi.org/10.1007/978-3-642-85376-0_11
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DOI: https://doi.org/10.1007/978-3-642-85376-0_11
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