Abstract | AIM AND METHODS: Data were collected from 3814 patients in this postmarketing surveillance study to assess the efficacy and tolerability of moxifloxacin. RESULTS: Improvement was observed in 69.1% of the patients after 3 days of moxifloxacin treatment and in 90.4% after 5 days. Full recovery had occurred in 71.3% by 7 days and in 86.8% by 10 days. A total of 129 adverse events occurred in 74 (1.9%) patients and mainly involved either the gastrointestinal or nervous system. All events were mild or moderate, and most resolved or improved after stopping treatment. Physicians rated moxifloxacin as 'good' or 'very good' in 92% of patients for efficacy and in 90.8% of the patients for tolerability. Of the 936 patients who completed a questionnaire, 94.7% stated that moxifloxacin had helped them, 95.5% reported an improvement in symptoms after 5 days and 97.7% reported symptom improvement after 10 days. CONCLUSIONS:
Moxifloxacin performs well in the 'real world', and is acceptable to both patients and physicians.
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Authors | L Y Liu, H Landen |
Journal | International journal of clinical practice
(Int J Clin Pract)
Vol. 61
Issue 9
Pg. 1509-15
(Sep 2007)
ISSN: 1368-5031 [Print] India |
PMID | 17635617
(Publication Type: Journal Article, Multicenter Study, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anti-Infective Agents
- Aza Compounds
- Fluoroquinolones
- Quinolines
- Moxifloxacin
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Topics |
- Adult
- Aged
- Anti-Infective Agents
(adverse effects, therapeutic use)
- Aza Compounds
(adverse effects, therapeutic use)
- China
- Female
- Fluoroquinolones
- Humans
- Male
- Middle Aged
- Moxifloxacin
- Product Surveillance, Postmarketing
(methods)
- Prospective Studies
- Quinolines
(adverse effects, therapeutic use)
- Respiratory Tract Infections
(drug therapy, pathology)
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