Skip to main content
. 2001 Dec;52(6):699–701. doi: 10.1046/j.1365-2125.2001.01489.x

Table 1.

Influence of UDCA and CDCA on the pharmacokinetics of nitrendipine in healthy subjects (mean ± s.d., (95% confidence interval for the difference), n = 6).

Treatment Cmax (ng ml−1) tmax (h) AUC(0,12 h) (ng ml−1 h) t (h)
Control 10.9 ± 5.8 1.7 ± 0.5 60 ± 36 3.7 ± 0.4
UDCA 50 mg 5.0 ± 4.7 1.2 ± 0.4 15 ± 13 2.7 ± 1.1
(3.9, 7.8, P = 0.0006) (−0.1, 1.1, P = 0.0756) (20, 73, P = 0.0064) (−0.8, 1.8. P = 0.3801)
CDCA 200 mg 8.7 ± 6.1 1.7 ± 0.5 49 ± 34 3.2 ± 0.9
(0.4, 3.8, P = 0.0230) (−0.7, 0.7, P = 1) (−2, 26, P = 0.0850) (−1.2, 1.1, P = 0.9178)
CDCA 600 mg 5.0 ± 3.9 1.8 ± 0.8 19 ± 19 2.9 ± 1.1
(2.6, 9.2, P = 0.0059) (−1.2, 0.9, P = 0.6952) (21, 63, P = 0.0038) (−1, 3, P = 0.8849)