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Most Commonly Reported Adverse Eventsa
| Adverse Event | Patients, No. (%) | |
|---|---|---|
| Darusentan (n=76) | Placebo (n=39) | |
| Peripheral edema | 13 (17) | 2 (5) |
| Headache | 8 (11) | 2 (5) |
| Sinusitis | 6 (8) | 0 |
| Dizziness | 5 (7) | 1 (3) |
| Nasopharyngitis | 5 (7) | 1 (3) |
| Upper respiratory tract infectionb | 4 (5) | 2 (5) |
| Gastroenteritis | 4 (5) | 1 (3) |
| Arthralgia/arthritis | 2 (3) | 6 (15) |
| Diarrhea | 1 (1) | 2 (5) |
| aOccurred in ≥5% of patients in a treatment group. bIncluded patients with symptoms of an upper respiratory tract infection. | ||
