Table 3. TEAEs that led to study withdrawal in ⩾1.0% of patients in either treatment group, stage 1 (SS; N=1055).
| PA21 (N=707) (%) | Sevelamer (N=348) (%) | |
|---|---|---|
| Any TEAE | 15.7 | 6.6 |
| Diarrhea | 2.8 | 0.6 |
| Nausea | 1.6 | 0.6 |
| Abnormal product taste | 1.6 | 0.3 |
| Hyperphosphatemia | 1.4 | 0.0 |
| Constipation | 1.0 | 1.4 |
| Vomiting | 1.0 | 0.6 |
Abbreviations: AE, adverse event; PA21, sucroferric oxyhydroxide; SS, safety set; TEAE, treatment-emergent AE.