Abstract
The pharmacokinetics of a single 400 mg oral dose of fleroxacin and pefloxacin were evaluated in ten healthy male volunteers in a randomized cross-over study. There were no significant differences in Tmax (0.9 vs. 1.3 h) and in plasma elimination half-life (11.9 vs. 10.8 h) between fleroxacin and pefloxacin. Cmax and AUC of fleroxacin were statistically significantly greater (P <0.05) compared to pefloxacin (C 5.62 vs. 4.09 mg/l, AUC0-48: 65.9 vs. 48.7 mg/l.h, AUC0-∞: 70.7 vs. 51.5 mg/1.h).Renal clearances of fleroxacin and pefloxacin were 51.8 and 11.7; ml/mim respectively. The 48-h urine recovery was 48.6% for fleroxacin, 8.6% for pefloxacin, 7.1% and 17.4% for the N-demethyl metabolites, and 3.8% and 16.6% for the N-oxide metabolites of fleroxacin and pefloxacin respectively. Urinary concentrations of both the microbiologically active parent drug and the N-demethyl meta bolite of fleroxacin were, at all intervals up to 48 h post dose, two to three times higher than those of pefloxacin. © 1988, by The British Society for Antimicrobial Chemotherapy.
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CITATION STYLE
De Lepeleire, I., Van Hecken, A., Verbesselt, R., Tjandra-maga, T. B., & De Schepper, P. J. (1988). Comparative oral pharmacokinetics of fleroxacin and pefloxacin. Journal of Antimicrobial Chemotherapy, 22(2), 197–202. https://doi.org/10.1093/jac/22.2.197
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