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Results of multi-center non-randomized, non-comparative trial of efficacy and safety of levofloxacin in moderate communityacquired pneumonia

Abstract

The article shows results of Russian multi-center trial of efficacy and safety of levofloxacin in moderate community-acquired pneumonia (CAP) patients took place from October, 2001, to November, 2002, at Moscow, Nizhny Novgorod, Samara, Ekaterinburg, Chelyabinsk, Tyumen and Irkutsk. The trial involved 77 patients (37 females and 40 males with the average age of 40.8±14.4 yrs) admitted to a hospital with the CAP. Levofloxacin was given in a standard dose of 500 meg once a day, the average length of the treatment was 9.2 days. The clinical efficacy of the single-therapy with levofloxacin was 98.7%. Adverse effects were noted in 4 cases (nausea was in 4 patients and headache was in 1 patient). The therapy was abolished in 1 case due to the adverse effects.

About the Authors

A. I. Sinopalnikov
Кафедра пульмонологии с курсом фтизиатрии Государственного института усовершенствования врачей МО РФ
Russian Federation


Yu. G. Belotserkovskaya
Кафедра пульмонологии с курсом фтизиатрии Государственного института усовершенствования врачей МО РФ
Russian Federation


A. G. Romanovskikh
Кафедра пульмонологии с курсом фтизиатрии Государственного института усовершенствования врачей МО РФ
Russian Federation


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Review

For citations:


Sinopalnikov A.I., Belotserkovskaya Yu.G., Romanovskikh A.G. Results of multi-center non-randomized, non-comparative trial of efficacy and safety of levofloxacin in moderate communityacquired pneumonia. PULMONOLOGIYA. 2003;(4):83-89. (In Russ.)

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ISSN 0869-0189 (Print)
ISSN 2541-9617 (Online)