Table 4.
Intravenous antibiotic therapy (n=126) |
Oral antibiotic therapy (n=146) |
Total (n=272) |
|||||
---|---|---|---|---|---|---|---|
Events | Participants | Events | Participants | Events | Participants | ||
Any non-serious adverse event* | 126 | 60 (48%) | 136 | 72 (49%) | 262 | 132 (49%) | |
Most common non-serious adverse events† | |||||||
Cough | 26 | 22 (17%) | 28 | 23 (16%) | 54 | 45 (17%) | |
Upper respiratory tract infection | 15 | 11 (9%) | 3 | 2 (1%) | 18 | 13 (5%) | |
Productive cough | 5 | 5 (4%) | 8 | 8 (5%) | 13 | 13 (5%) |
Data are n or n (%).
Nine additional adverse events were reported by nine participants in the intravenous antibiotic therapy group and five adverse events from five participants in the oral antibiotic therapy group but have not been included here as they were the event of interest for the primary outcome (P aeruginosa isolation) so should not have been reported as an adverse event. Three additional adverse events were reported by three participants in the oral antibiotic therapy group but have not been included here as they contributed to the analysis of the outcome number of pulmonary exacerbations.
Reported by at least 5% of participants in either treatment group.