Table 5.
Adverse events in both treatment groups for a 6-month study period.
Adverse event | Aranesp | Eprex | P-value * |
Vascular access thrombosis | 0 (0%) | 3 (5%) | 0.064 |
High blood pressure | 6 (9%) | 7 (11.7%) | 0.615 |
Stroke | 0 (0%) | 1 (1.7%) | 0.289 |
Myocardial infarction | 1 (1.5%) | 1 (1.7%) | 0.937 |
Vomiting | 2 (3%) | 3 (5%) | 0.560 |
Nausea | 4 (6%) | 5 (8.3) | 0.604 |
Diarrhea | 1 (1.5%) | 0 (0%) | 0.342 |
Edema | 2 (3%) | 1 (1.7%) | 0.625 |
Pain at the site of the injection | 7 (10.4) | 9 (15%) | 0.440 |
P-values were obtained by a chi-square test.