Table 3.
Summary of adverse events in the safety populationa
| Parameter | Ferumoxytol (n = 217) | Oral Iron (n = 75) | ||
|---|---|---|---|---|
| Events (n) | Patients (n [%]) | Events (n) | Patients (n [%]) | |
| Adverse events | 158 | 77 (35.5) | 102 | 39 (52.0) |
| Related adverse events | 41 | 23 (10.6) | 25 | 18 (24.0) |
| Serious adverse events | 15 | 10 (4.6) | 11 | 7 (9.3) |
| Related serious adverse events | 0 | 0 (0.0) | 0 | 0 (0.0) |
Patients who received at least one dose of study drug.