Abstract
In hospitalized patients serious infectious diseases are traditionally treated using intravenous antimicrobial agents with conversion to oral drugs, often occurring late in the course of therapy. Because of cost-containment pressures the concept of switching to oral agents early in the course of antibiotic therapy is important, and this has become a major goal of antibiotic monitoring programs [1–10]. In several of these programs [1, 6, 8] particular attention has been placed on oral fluoroquinolones, for these agents exhibit favorable pharmacokinetic and microbiologic characteristics, have shown efficacy in the treatment of a variety of infectious diseases [1, 11], and can reduce the cost of antibiotic therapy [12–17].
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Nightingale, C.H., Belliveau, P.P., Quintiliani, R. (1994). Conversion from Intravenous to Oral Ciprofloxacin: Observing the “Like-to-Like” Phenomenon. In: Garrard, C. (eds) Ciprofloxacin i.v.. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-79098-0_8
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DOI: https://doi.org/10.1007/978-3-642-79098-0_8
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