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Open-label crossover study to determine pharmacokinetics and penetration of two dose regimens of levofloxacin into inflammatory fluid.

Two levofloxacin administration regimens were used for six healthy male volunteers. They received either 500 mg of levofloxacin orally every 12 h for five doses or 500 mg every 24 h for three doses, and then 6 weeks later they received the other course. The concentrations of the drug in plasma, cant...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Antimicrob Agents Chemother
Principais autores: Child, J, Mortiboy, D, Andrews, J M, Chow, A T, Wise, R
Format: Artigo
Jezik:Inglês
Izdano: American Society for Microbiology (ASM) 1995
Teme:
Online dostop:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC163023/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8593013/
https://ncbi.nlm.nih.govhttps://doi.org/10.1128/aac.39.12.2749
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