In the last decade three important pharmacodynamic parameters: T>MIC, C-max
/MIC and AUC/MIC, have been shown to correlate well with in-vitro antimicro
bial efficacy and that found in animal models, differentiating among groups
of antibiotics with diverse mechanisms of action such as exposure time or
concentration-dependent effect. The macrolide antimicrobial agents display
variable concentration-dependent killing, indicating the increasing importa
nce of the C-max parameter, Clarithromycin, whose T>MIC and AUC influence i
ts clinical efficacy, is in an intermediate position between its progenitor
, erythromycin, and the azalides, This paper reviews pharmacokinetic and Dh
armacodynamic characteristics of clarithromycin, examining the potential im
pact of these properties on the dose and the optimal interval between admin
istrations.