TABLE 3.
ADVERSE EVENTS IN THE RESOLVE TRIAL BASED ON IL-8 STRATIFICATION
IL-8 ≤ 220 pg/ml (n = 72) | IL-8 > 220 pg/ml (n = 121) | P Value | |
---|---|---|---|
Serious adverse events, n (%) | |||
Day 0 to 6 | 5 (6.9) | 11 (9.1) | 0.6* |
Day 0 to 28 | 12 (16.7) | 21 (17.4) | 0.9* |
Serious bleeding events, n (%) | |||
Day 0 to 6 | 0 (0) | 4 (3.3) | 0.3† |
Day 0 to 28 | 1 (1.4) | 9 (7.4) | 0.09† |
Serious bleeding events, n (%) | |||
Day 0 to 6 | 0 (0) | 0 (0) | — |
Day 0 to 28 | 1 (1.4) | 4 (3.3) | 0.6† |
χ2.
Fisher exact test.