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. 2007 Mar 1;64(2):125–132. doi: 10.1111/j.1365-2125.2007.02867.x

Table 1.

Population pharmacokinetic parameters for budesonide after a single dose of 1600μg in healthy volunteers using a mixed effects model

Parameters Estimate Relative SE Brief definition of symbols
CL (l h−1) 81.5 Clearance for budesonide
V (l) 219 Volume of distribution of budesonide
ka (h−1) 3.72 First order absorption rate constant for budesonide
ω CL 38% 14% Interindividual variability for CL (%CV)
ωV 39% 15% Interindividual variability for V (%CV)
ωka 25% 41% Interindividual variability for ka(%CV)
σ 14% 2% Proportional error (%CV)
OFV −216 Objective function value