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Comparative bioavailability of disopyramide after multiple dosing with standard capsules and controlled-release tablets

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Summary

Plasma concentrations and bioavailability of disopyramide following repeated administration of standard capsules and controlled-release tablets have been compared. Ten patients were randomized into two groups; Group I received disopyramide capsules 150 mg every 6 h for five days and subsequently disopyramide controlled-release tablets 300 mg every 12 h for further five days. Group II received the same preparations in the reverse order. There was a more rapid rise in disopyramide concentration after the capsules: the maximum of 10.7±0.6 µmol/l (mean ± SEM) was reached within 1.8±0.4 h as compared to 10.6±0.4 µmol/l within 4.0±0.3 h after the controlled-release tablets. No significant difference in the fluctuations in individual plasma concentrations during each dose interval at steady state were observed after ordinary capsules compared to controlled-release tablets. The extent of bioavailability was the same. Eight patients reported some side-effects during the capsule period and nine during the controlled-release tablet period.

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Forssell, G., Graffner, C., Nordlander, R. et al. Comparative bioavailability of disopyramide after multiple dosing with standard capsules and controlled-release tablets. Eur J Clin Pharmacol 17, 209–213 (1980). https://doi.org/10.1007/BF00561902

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  • DOI: https://doi.org/10.1007/BF00561902

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