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1 (ie, PK) can be influenced by adjusting the dosage regimen.
2 um drug concentrations reported for standard dosage regimens.
3 fewer bleeding complications than do higher dosage regimens.
4 e of subcutaneous veltuzumab, using the same dosage regimen, again induced complete remission off the
5 and glomerular endothelial cells across all dosage regimens, and clearance of podocyte inclusions is
8 crobial drug development and optimization of dosage regimens, but systematic simulation-estimation st
9 of whole brain mitosis, suggesting that the dosage regimen did not elicit a cytotoxic, wound-healing
11 dence as to whether growth hormone in modern dosage regimens is associated with an increased risk of
15 to mimic four different clinically relevant dosage regimens of polymyxin B and colistin over 96 h.
16 Polymyxin resistance was observed across all dosage regimens; partial reversion to susceptibility was
17 dministration at 4 testing sessions, using a dosage regimen shown to induce sensitization (ie, 3 dose
19 postnatal days (PN) 30 through 47.5, using a dosage regimen that maintains plasma levels similar to t
22 l susceptible individuals and development of dosage regimens that maintain effective antimicrobial dr
23 with a major objective being to derive drug dosage regimens that optimize efficacy and minimize toxi
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