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Table 2 Patient safety data through week 9

From: Clinical efficacy and IL-17 targeting mechanism of Indigo naturalis as a topical agent in moderate psoriasis

 

Placebo

Indigo naturalis

Patients treated, n

8

16

Patients with >1 adverse event, n (%)

4 (50.0)

7 (44.0)

Average duration of follow-up (weeks)

9.14

9.13

Average exposure (weeks)

8.16

8.13

Common adverse events, n (%)

 Pruritus

1 (12.5)

4 (25.0)

 Rash

0 (0.0)

2 (12.5)

 Nasopharyngitis

0 (0.0)

2 (12.5)

 Abdominal distension

0 (0.0)

1 (6.3)

 Constipation

0 (0.0)

1 (6.3)

 Cough

0 (0.0)

1 (6.3)

 Dizziness

0 (0.0)

1 (6.3)

 Oropharyngeal pain

0 (0.0)

1 (6.3)

 Gout

1 (12.5)

0 (0.0)

 Allergies

1 (12.5)

0 (0.0)

 Pyrexia

1 (12.5)

0 (0.0)