Table 3.
Reported Adverse Events During Tildrakizumab Treatment Up to 52 Weeks Follow-Up
| Adverse Events | |
|---|---|
| Pharyngitis | 11.9% (n=5) |
| Flu-like illness | 9.5% (n = 4) |
| Headache | 7.1% (n = 3) |
| Diarrhoea | 2.4% (n=1) |
| Injection site reaction (pain) | 7.1% (n = 3) |
Reported Adverse Events During Tildrakizumab Treatment Up to 52 Weeks Follow-Up
| Adverse Events | |
|---|---|
| Pharyngitis | 11.9% (n=5) |
| Flu-like illness | 9.5% (n = 4) |
| Headache | 7.1% (n = 3) |
| Diarrhoea | 2.4% (n=1) |
| Injection site reaction (pain) | 7.1% (n = 3) |