Skip to main content
. 1998 Mar;42(3):631–639. doi: 10.1128/aac.42.3.631

TABLE 3.

Pharmacokinetic parameters of clarithromycin and 14-OH-clarithromycin for 11 subjects receiving regimen Aa

Drug AUC0–τ (μg · h/ml)
Mean % change in AUC0–τ between days 14 and 42 (P value) Cmax (μg/ml)
Mean % change in Cmax between days 14 and 42 (P value) Tmax (h)
Mean % change in Tmax between days 14 and 42 (P value)
Day 14 Day 15 Day 42 Day 14 Day 15 Day 42 Day 14 Day 15 Day 42
Clarithromycin 36.5 ± 15.0 35.5 ± 15.8 16.6 ± 5.4 −44 ± 37 (0.003) 5.7 ± 2.4 4.6 ± 1.7 2.8 ± 1.0 −41 ± 35 (0.003) 3.0 ± 2.3 3.2 ± 2.2 3.5 ± 3.2 34 ± 100 (0.287)
14-OH-Clarithromycin 9.1 ± 3.4 9.2 ± 3.7 13.4 ± 5.0 57 ± 51 (0.004) 1.1 ± 0.4 1.0 ± 0.4 1.7 ± 0.6 69 ± 49 (<0.001) 3.6 ± 2.8 3.1 ± 2.4 4.6 ± 3.6 52 ± 106 (0.136)
Rifabutin 8.6 ± 8.2b 6.1 ± 1.9 0.59 ± 0.33 0.54 ± 0.19 3.7 ± 1.1 3.8 ± 3.4
25-O-Desacetyl-rifabutin 2.3 ± 1.2b 1.5 ± 0.7 0.10 ± 0.06 0.12 ± 0.06 5.3 ± 1.2 4.4 ± 3.0
a

Study day 14 is steady state for clarithromycin alone, day 15 is the first day that rifabutin was added to the regimen, and day 42 is steady state for both drugs. All values are means ± standard deviations. 

b

The AUC reported for rifabutin and its metabolite on day 15 represents AUC0–∞