Mh. Devries et al., PHARMACOKINETICS OF FLUVOXAMINE MALEATE AFTER INCREASING SINGLE ORAL DOSES IN HEALTHY-SUBJECTS, Biopharmaceutics & drug disposition, 14(4), 1993, pp. 291-296
The pharmacokinetics of fluvoxamine after single oral administration o
f 25, 50, and 100 mg fluvoxamine maleate was studied in a three-way cr
oss-over study in 12 healthy male subjects. Fluvoxamine was administer
ed orally in a solution. For dose-proportionality, AUC, and C(max)-dos
e relationships were evaluated by linear regression. Plasma concentrat
ions increased in a linear dose-dependent manner in the dose range bet
ween 25 and 100 mg; t1/2 and T(max) showed no significant differences
among treatments. Fluvoxamine was well tolerated.