This study is a post-marketing surveillance in Japan to investigate the safety especially focusing on injection site adverse events and efficacy in patients with Ciprofloxacin iv administration without dilution in the daily practice.It is a local prospective and observational study of patients who have received Ciproxan intravenously for sepsis, secondary skin infections followed by superficial burn, post-surgical or post-traumatic, pneumonia, peritonitis, cholecystitis, cholangitis, anthrax. A total of 500 patients are to be enrolled and assessed during the period of treatment with Ciproxan.
Study Type
OBSERVATIONAL
Enrollment
704
Patient treated with Ciproxan without dilution treatment in daily clinical practice
Unnamed facility
Many Locations, Japan
Incidence of adverse drug reactions (ADRs) and serious adverse events (AEs)
Time frame: After 8 days
Clinical efficacy by four grade (Response, Minor Response, No Response, and Indeterminable) at an investigator discretion
Time frame: After 8 days
ADR incidence rates classified by patient's background factors
Time frame: After 8 days
Efficacy rate calculated with Response and Minor Response considered as responder
Time frame: After 8 days
Efficacy rates classified by patient's background factors
Time frame: After 8 days
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