Table 2 Number (%) of patients with adverse events during the double-blind period (2% in any group, safety population)
Preferred term n (%) | Aliskiren 300 mg (N=331) | Aliskiren 150 mg (N=323) | Aliskiren 75 mg (N=332) | Ramipril 5 mg (N=329) |
---|---|---|---|---|
Any AEs | 52 (15.7) | 60 (18.6) | 57 (17.2) | 68 (20.7) |
AE >2% in any group | ||||
Dizziness | 10 (3.0) | 15 (4.6) | 15 (4.5) | 13 (4.0) |
Headache | 6 (1.8) | 13 (4.0) | 6 (1.8) | 12 (3.6) |
Cough | 4 (1.2) | 3 (0.9) | 2 (0.6) | 17 (5.2) |
Discontinuation because of AEs | 9 (2.7) | 16 (5.0) | 14 (4.2) | 8 (2.4) |
Any SAE | 1 (0.3) | 2 (0.6) | 3 (0.9) | 1 (0.3) |