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. 2011 May;55(5):2122–2128. doi: 10.1128/AAC.01504-10

Table 3.

Main urinary rifamycin SV PK parameters of the different regimensa

Treatment Interval (h) Xu (ng) dXu/dt (ng/h) ΣXu (ng) ΣXu (% of dose)
Single oral 400-mg dose under fasting conditions 0–6 <0.1 <0.1 3,966.1 ± 6,166.3 0.0010 ± 0.0015
6–12 1,612.8 ± 3,338.4 268.8 ± 556.4
12–24 2,353.4 ± 3,221.4 196.1 ± 268.5
Single oral 400-mg dose under fed conditions 0–6 <0.1 <0.1 1,500.5 ± 3,049.1 0.0004 ± 0.0008
6–12 103.2 ± 335.7 17.2 ± 55.9
12–24 1,397.3 ± 2,990.5 116.4 ± 249.2
Oral 800-mg dose (200 mg q.i.d.) 0–3 1,873.9 ± 1,405.8 624.6 ± 468.6 7,172.7 ± 4,180.0 0.0036 ± 0.0021
3–6 1,611.1 ± 931.2 537.0 ± 310.4
6–12 3,687.7 ± 2,377.6 614.6 ± 396.3
Oral 800-mg dose (400 mg b.i.d.) 0–3 3,216.9 ± 2,437.2 1,072.3 ± 812.4 10,914.5 ± 5,309.3 0.0027 ± 0.0013
3–6 2,713.3 ± 1,249.5 904.4 ± 416.5
6–12 4,984.3 ± 3,029.6 830.7 ± 504.9
a

Values are means ± SD. Shown are the amount of excretion (Xu) (expressed in ng and as a percentage), the rate of excretion (dXu/dt), and the total amount of excretion (ΣXu) (expressed in ng and as a percentage) after a single dose (n = 22) and multiple oral doses (n = 12) of rifamycin SV MMX (200-mg tablets).