TABLE 5.
Adverse event | No. (%) of subjects in: |
|
---|---|---|
Single-ascending-dose study (n = 42) | Multiple-ascending-dose study (n = 24) | |
Any event | 19 (45.2) | 21 (87.5) |
Diarrhea | 0 | 4 (12.5) |
Headache | 3 (5.4) | 6 (18.8) |
Infusion site discomfort | 0 | 7 (21.9) |
Infusion site pain | 2 (3.6) | 11 (34.4) |
Infusion site erythema | 1 (1.8) | 10 (41.7) |
Nausea | 8 (14.3) | 11 (45.8) |
Pain in extremity | 2 (3.6) | 5 (15.6) |
Phlebitis superficial | 0 | 14 (43.8) |