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Twice-daily dosing was statistically superior.
Dosing was conducted daily beginning on day 8 postpartum.
Scheduled dosing was associated with decreased pain intensity ratings.
Mean absorption time (MAT) after s.c. dosing was also prolonged (p = 0.006).
Dosing was at intervals of at least two weeks in a 5 × 5 Latin square design.
The mean bioavailability following intramuscular and subcutaneous dosing was 84.5 and 104.2%, respectively.
Dosing was independent of body weight.
Drug dosing was similar in the two groups.
Dosing was initiated at 225 mg/day and increased to 450 mg/day as tolerated.
Dosage-dependent reductions were observed when different maltodextrin/2IB3MP dosing was compared.
Vancomycin dosing was dictated by the treating clinician, and therapy could be administered either via II or CI.
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