The objective of this study is to assess the efficacy and safety of Avelox Tablet 400 mg (hereinafter as "Avelox") in treating secondary infection of chronic respiratory disease.It is a local prospective and observational study of patients who have received Avelox tablets for Laryngopharyngitis, Tonsillitis, Bronchitis acute, Pneumonia, Secondary infection in chronic respiratory diseases, Sinusitis. A total of 500 patients are to be enrolled and assessed during the period of treatment with Avelox.
Study Type
OBSERVATIONAL
Enrollment
497
Patients treated with Moxifloxacin in daily clinical practice
Unnamed facility
Multiple Locations, Japan
Number of adverse drug reactions (ADRs) and serious adverse events (SAEs)
Time frame: After 7 days
Clinical efficacy rate (Response, Minor Response, No Response and Indeterminable) assessed by investigator's discretion. Efficacy rate is calculated as number of patients with Response or Minor Response proportional to number of all cases.
Time frame: After 7 days
ADR incidence rates classified by patient's background factors
Time frame: After 7 days
Efficacy rates classified by patient's background factors
Time frame: After 7 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.