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. Author manuscript; available in PMC: 2016 Jan 31.
Published in final edited form as: Clin Pharmacol Ther. 2014 Dec 4;97(2):167–176. doi: 10.1002/cpt.5

Table 2.

Ondansetron population pharmacokinetic parameter estimates.

Parameters Point
estimate
(%SE)
Symmetrical
95% CI
Nonsymmetrical
95% CI
Residual
variability
(%CV)
Between-subject
variability
(%CV)
Women: 21.6

CL (L/h) 40.1
  CL0 21.8 (6.7) 18.9, 24.6 17.2, 27.2
  θCL 0.69 (11) 0.54, 0.84 0.52, 0.92

V (L) 27.9 (17) 18.5, 37.3 13.6, 45.0 56.1

Q(L/h) 329 (9.5) 268, 390 256, 401 51.3

VSS (L) 32.4
  VSS0 167 (4.7) 151, 182 140, 198
  θVss 0.75 (7.8) 0.63, 0.86 0.61, 0.91

Cord: 23.5

KP 0.47 (5.1) 0.42, 0.52 0.44, 0.51

Neonates: 21.9

KN0 (1/h) 0.046 (6.2) 0.041, 0.052 0.040, 0.052 29.6

%SE: relative standard error; CV: coefficient of variation; CI: confidence interval; CL clearance in women; CL0 clearance for 4-mg dose; θCL fractional change in CL0 for the 8-mg dose; V distribution volume in women; Q inter-compartmental clearance in women; KP placenta-to-