Table 2.
Placebo group (n = 39) | Topiroxostat 120-mg group (n = 39) | Topiroxostat 160-mg group (n = 40) | Allopurinol group (n = 39) | |||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Adverse event | Adverse drug reaction | Adverse event | Adverse drug reaction | Adverse event | Adverse drug reaction | Adverse event | Adverse drug reaction | |||||
Number of subjects | 29 | 15 | 28 | 8 | 25 | 7 | 23 | 10 | ||||
Incidence (%) | 74.4 | 38.5 | 71.8 | 20.5 | 62.5 | 17.5 | 59.0 | 25.6 | ||||
χ 2 test | P vs. 120 | P vs. 160 | 120 vs. 160 | P vs. Allo | 120 vs. Allo | 160 vs. Allo | P vs. 120 | P vs. 160 | 120 vs. 160 | P vs. Allo | 120 vs. Allo | 160 vs. Allo |
P | 0.799 | 0.257 | 0.379 | 0.150 | 0.234 | 0.748 | 0.082 | 0.038* | 0.733 | 0.225 | 0.591 | 0.379 |
Incidence (%) number of adverse events- and/or adverse drug reaction-observed subjects/number of subjects for safety evaluation
*P < 0.05