P. Villani et al., Pharmacokinetic evaluation of oral levofloxacin in human immunodeficiency virus-infected subjects receiving concomitant antiretroviral therapy, ANTIM AG CH, 45(7), 2001, pp. 2160-2162
The purpose of this study was to evaluate the pharmacokinetics (PK) profile
of oral levofloxacin in human immunodeficiency virus-positive patients in
steady-state treatment with nelfinavir (NFV) or with efavirenz (EFV) and to
determine the effects of levofloxacin on the PR parameters of these two an
tiretroviral agents. For levofloxacin, plasma samples were obtained at stea
dy state during a 24-h dosing interval. Plasma NFV and EFV concentrations w
ere evaluated before and after 4 days of levofloxacin treatment. Levofloxac
in PI( do not seem affected by NFV and EFV. There was no significant differ
ence between NFV and EFV plasma levels obtained with and without levofloxac
in.