Table 2.
Adverse events during two month follow-up
| Adverse event | HLA-B*58:01 positive participants receiving alternative drug treatment (n=354) | HLA-B*58:01 negative participants receiving allopurinol (n=2173) | Total (n=2910) |
|---|---|---|---|
| Mild cutaneous events | |||
| Rash and itching | 3* | 94 | 97 |
| Blisters | 0 | 0 | 0 |
| Oral ulcers | 0 | 2 | 2 |
| Rash, itching, oral ulcers, and fever | 0 | 1 | 1 |
| Rash, itching, and other adverse events | 0 | 22 | 22 |
| Severe cutaneous events | |||
| Drug reaction with eosinophilia and systemic symptoms | 0 | 0 | 0 |
| Urticaria | 0 | 0 | 0 |
| Stevens-Johnson syndrome or toxic epidermal necrolysis | 0 | 0 | 0 |
| Other adverse events† | |||
| Fever | 0 | 1 | 1 |
| Sore throat | 0 | 2 | 2 |
| Fatigue | 0 | 5 | 5 |
| Other | 20 | 117 | 137 |
Data are no of participants having adverse events.
*All three participants took benzbromarone.
†Each participant may have had more than one adverse event. Adverse events with a low frequency are not listed.