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. 2020 Nov 24;28(4):181–188. doi: 10.12793/tcp.2020.28.e17

Table 2. Comparison of the pharmacokinetic parameters of tamsulosin 0.2 and 0.4 mg capsules in the fed state.

Pharmacokinetic parameters Tamsulosin 0.4 mg under fed state (n = 22) Tamsulosin 0.2 mg under fed state (n = 22) Geometric mean ratio (90% confidence interval)
Tmax (h) 5.00 [3.00–10.00] 6.00 [4.00–10.00]
Cmax (μg/L) 13.43 ± 4.11 5.51 ± 1.76 2.41 (2.18–2.68)
AUClast (h·μg/L) 185.94 ± 56.30 90.76 ± 25.01 2.04 (1.93–2.18)
AUCinf (h·μg/L) 199.61 ± 66.57 100.30 ± 29.67 1.98 (1.86–2.11)
Cmax/dose (/L) 0.034 ± 0.010 0.028 ± 0.009 1.21 (1.09–1.34)
AUClast/dose (h/L) 0.46 ± 0.14 0.45 ± 0.13 1.02 (0.96–1.09)
AUCinf/dose (h/L) 0.50 ± 0.17 0.50 ± 0.15 0.99 (0.93–1.06)
Vz/F (L) 34.35 ± 11.11 39.10 ± 13.87
CL/F (L/h) 2.22 ± 0.76 2.22 ± 0.82
t1/2 (h) 11.19 ± 3.02 12.56 ± 2.32

Data are presented as the mean ± standard deviation except for Tmax which is expressed as the median [minimum-maximum].

Cmax, maximum plasma concentration; Tmax, time of maximum plasma concentration; AUClast, area under the curve from the time of administration to last measurable concentration; AUCinf, AUC from administration to infinity based on the last concentration; Cmax/dose, dose-normalized maximum plasma concentration; AUClast/dose, dose-normalized AUClast; AUCinf/dose, dose-normalized AUCinf; Vz/F, apparent volume of distribution during the terminal phase; CL/F, apparent clearance; t1/2, terminal elimination half-life.