Objective: To investigate the pharmacokinetics of levofloxacin and the pharmacokinetic-pharmacodynamic appropriateness of its total body exposure in patients in the intensive care unit (ICU) treated for early-onset ventilator-associated pneumonia (VAP) with intravenous levofloxacin 500mg twice daily.
Design: Prospective non-blinded pharmacokinetic-pharmacodynamic study.
Participants: Ten critically ill adult patients with normal renal function.