Skip to main content
. 2016 Nov 21;60(12):7035–7042. doi: 10.1128/AAC.01567-16

TABLE 3.

Final overall model pharmacokinetic parametersa

Author(s), yr (reference no.) AUC (mg · h/liter) Cmax (mg/liter) kel (h−1) t1/2b (h) Tmax (h) Absorption t1/2 (h) Ka (h−1) V/F (liters) CL/F (liters/h)
Overall 51.31 (45.01, 60.28) 2.19 (2.06, 2.33) 0.05 (0.04, 0.06) 13.27 (11.79, 15.42) 2.93 (2.57, 3.48) 0.60 (0.38, 1.11) 1.16 (0.59, 1.76) 39.19 (36.58, 42.17) 2.04 (1.77, 2.32)
Bronn, 2015 (17) 50.05 (45.91, 54.34) 2.20 (2.06, 2.34) 0.05 (0.05, 0.06) 12.95 (12.03, 13.95) 2.75 (2.41, 3.17) 0.59 (0.49, 0.72) 1.18 (0.96, 1.41) 39.16 (36.69, 42.04) 2.09 (1.93, 2.29)
Peregrina Lucano, 2004 (20) 54.82 (48.20, 64.40) 2.11 (1.92, 2.29) 0.05 (0.04, 0.06) 14.02 (12.26, 16.66) 3.65 (2.77, 5.27) 0.85 (0.58, 1.44) 0.82 (0.48, 1.20) 39.38 (36.79, 42.55) 1.95 (1.65, 2.23)
Raaflaub and Ziegler, 1979 (22) 49.76 (44.66, 55.38) 2.26 (2.09, 2.44) 0.05 (0.05, 0.06) 12.94 (11.84, 14.28) 2.35 (1.92, 2.93) 0.47 (0.36, 0.64) 1.46 (1.08, 1.92) 39.04 (36.27, 42.01) 2.09 (1.87, 2.33)
a

Data represent the mean (95% CrI).

b

t1/2, half-life.