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. 2004 Sep;58(3):259–268. doi: 10.1111/j.1365-2125.2004.02143.x

Table 3.

Summary of pharmacokinetic data for vancomycin 750 mg i.v. every 12 h

Patient profile Cmax(mg l−1) t1/2(β) (h) AUC0–12(mg h l−1) AUC0–(mg h l−1) Cl (l h−1) Vss(l) F12 (%)
1A 67.8 7.8 243.4 344.0 2.2 20.3 71
1B 55.0 25.2 406.7 1.8 66.5 NA
2A 42.9 9.7 210.6 362.5 2.1 27.5 58
2B 43.4 18.3 318.1 2.4 57.1 NA
3A 47.2 6.2 196.8 265.6 2.8 22.8 74
3B 47.2 22.6 367.6 2.0 64.7 NA
4B 36.3 11.8 243.9 3.1 51.6 NA
5A 54.0 13.5 243.6 509.3 1.5 27.1 48
6B 49.0 17.1 300.8 2.5 56.3 NA
7B 53.8 22.1 350.1 2.1 62.9 NA
8A 39.8 10.9 190.6 344.9 2.2 31.8 55
8B 44.9 38.3 283.8 2.6 136.7 NA
9B 32.6 6.0 171.9 4.4 29.9 NA
10A 27.1 11.5 115.6 205.6 3.6 53.4 56
10B 39.6 12.8 293.4 2.6 36.9 NA
Mean ± SD 15.6 ± 8.7 2.5 ± 0.7 49.7 ± 29.1 60 ± 10

Patient profile each separate occasion that pharmacokinetics were studied (e.g. 1B is second occasion for patient 1). Cmax, Maximum vancomycin plasma concentration; t1/2(β) elimination half life; AUC0−12, areas under the curve for study period; AUC0–, area under the curve extrapolated to infinity; CL, total body clearance; Vss, volume of distribution at steady state; F12, fraction of vancomycin eliminated within dosing interval of initial or first dose (Profile A only); NA, not applicable.