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Bleeding Events in the APEX Study Occurring ≤7 Days After Discontinuation of Study Drug.1
| Bleeding event | Betrixaban (n = 3716) | Enoxaparin (n = 3716) | Betrixaban versus Enoxaparin relative risk |
|---|---|---|---|
| Major bleeding | |||
| Any | 0.67% | 0.57% | 1.19 (95% CI, 0.67-2.12) (P = .554) |
| Gastrointestinal bleeding | 0.51% | 0.24% | |
| Intracranial hemorrhage | 0.05% | 0.19% | |
| Intraocular bleeding | 0% | 0.03% | |
| Fatal bleeding | 0.03% | 0.03% | |
| Clinically relevant nonmajor bleeding | |||
| Any | 2.45% | 1.02% | 2.39 (95% CI, 1.64-3.49) (P < .001) |
