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. Author manuscript; available in PMC: 2008 Jul 1.
Published in final edited form as: Drug Metab Dispos. 2008 Mar 31;36(7):1242–1248. doi: 10.1124/dmd.108.020396

Table 5.

Model-based population pharmacokinetic parameters of flurbiprofen.

Parameter Estimate 95% Confidence Interval
CL2C9, uninhibited (L/hr)
CYP2C9*1/*1 1.38 (1.15, 1.61)
CYP2C9*1/*3 0.805 (0.580, 1.03)
CYP2C9*3/*3 0.384 (0.215, 0.553)
CLnon2C9 (L/hr) 0.198 (0.0792, 0.317)
V (L) 8.40 (7.34, 9.46)
Ka (hr−1) 2.13 (1.18, 3.08)
LAG (hr) 0.200 (0.181, 0.219)
Variability (CV%)
CL 25.6% (5.9, 35.8%)
V 26.1% (12.4, 34.6%)
Ka 94.2% (63.1, 117%)
LAG 14.0% (1.4, 19.7%)
RUV 47.7% (43.5, 51.7%)

V- flurbiprofen volume of distribution, Ka — flurbiprofen first-order absorption rate constant, LAG — flurbiprofen absorption lag time, RUV — residual unexplained variability, CV — coefficient of variation