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. 2004 May;57(5):552–562. doi: 10.1111/j.1365-2125.2003.02062.x

Table 3.

Summary of ephedrine pharmacokinetic parameters for all three doses of ephedrine sulphate (0.25, 0.50, 1.0 mg kg−1)

Subject ka (h−1) CL/F(l h−1 kg−1) V/F(l kg−1) tlag (min)
1 1.30 0.39 4.4 5.2
2 0.94 0.46 4.4 13.2
3 1.50 0.38 4.5 12.6
4 0.96 0.51 4.5 6.1
5 0.89 0.50 4.6 2.4
6 0.84 0.37 3.4 8.7
7 0.86 0.43 3.6 5.5
8 0.29 0.72 2.5 2.1
Mean 0.95 0.47 4.0 7.0
SD 0.36 0.11 0.8 4.2
Pooled* 0.93 0.45 4.2 7.1

ka, rate constant of absorption; CL/F, apparent oral clearance; V/F, apparent volume of distribution; tlag, lag time;

*

parameter derived from modelling data from all subjects (n = 8).