Table 2.
No. (%) of participants with AE | Total number of AEs | |
---|---|---|
All | 8 (80%) | 55 |
Related to intervention | 5 (50%) | 18 |
-Grade 1 (mild) | 4 (40%) | 15 |
-Grade 2 (moderate) | 3 (30%) | 3 |
-Grade 3–5 (severe-death) | 0 (0%) | 0 |
-Cardiac disorder | 0 (0%) | 0 |
-Soreness/pain | 4 (40%) | 10 |
-Fatigue | 2 (20%) | 3 |
-Nausea | 0 (0%) | 0 |
-Lightheadedness | 2 (20%) | 5 |
-Other nervous system | 0 (0%) | 0 |
-Fall | 0 (0%) | 0 |
-Other | 0 (0%) | 0 |
Possibly related or unrelated to intervention | 8 (80%) | 37 |
-Grade 1 (mild) | 8 (80%) | 34 |
-Grade 2 (moderate) | 3 (30%) | 3 |
-Grade 3–5 (severe-death) | 0 (0%) | 0 |
-Cardiac disorder | 0 (0%) | 0 |
-Soreness/pain | 7 (70%) | 14 |
-Fatigue | 0 (0%) | 0 |
-Nausea | 0 (0%) | 0 |
-Lightheadedness | 3 (30%) | 6 |
-Other nervous system | 0 (0%) | 0 |
-Fall | 5 (50%) | 11 |
-Headache | 2 (20%) | 2 |
-Increased knee hyperextension | 1 (10%) | 1 |
-Joint stiffness | 1 (10%) | 1 |
-Infection (common cold) | 1 (10%) | 1 |
-Excision of ingrown toenail | 1 (10%) | 1 |
-Other | 0 (0%) | 0 |
There were no adverse events among control participants.