Skip to main content
. 2011 Dec;55(12):5780–5789. doi: 10.1128/AAC.05010-11

Table 3.

Individual voriconazole exposure parameters in young adolescents receiving 300 mg orally q12ha

Subject (age [yr], sex)b Wt (kg) CYP2C19 type IV steady state
Oral steady state
AUC0–12 (μg·h/ml) Cmax (μg/ml) AUC0–12 (μg·h/ml) Cmax (μg/ml)
23 (12, F) 30.4 HEM 40.1 9.82 NA NA
26 (12, M)c 39.0 UM 2.47 0.53 4.63 1.91
9 (12, F)d 39.8 EM 6.27 2.26 1.17 0.18
25 (13, M) 43.0 UM 8.29 2.44 14.6 2.84
21 (13, M) 50.8 EM 16.3 2.95 14.8 1.96
24 (13, M) 52.1 NA 49.9 4.87 15.5 2.09
12 (13, F) 53.4 HEM 16.7 2.61 12.1 1.63
6 (12, M) 56.8 HEM 37.2 4.69 26.5 3.59
4 (14, M) 58.7 HEM 8.14 2.06 5.59 0.81
1 (14, M)e 60.0 EM 10.4 2.5 11.9 1.54
7 (14, M) 65.5 HEM 17 3.24 15.8 2.18
a

The subset with AUC0-12 of <16 μg·h/ml.

b

EM, homozygous extensive metabolizer; F, female; HEM, heterozygous extensive metabolizer; M, male; NA, not available; UM, ultrarapid extensive metabolizer.

c

This subject inadvertently received phenytoin 2 days prior to the first dose until day 5 of IV treatment.

d

This subject received 150 mg orally q12h (a reduced dose for subjects weighing less than 40 kg).

e

This subject missed the morning doses on the fourth day and sixth day of oral voriconazole.