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Table 3 Summary of adverse events, patients discontinued due to adverse events and deaths

From: Treatment of plaque psoriasis with an ointment formulation of the Janus kinase inhibitor, tofacitinib: a Phase 2b randomized clinical trial

 

2 % tofacitinib BID

1 % tofacitinib BID

Vehicle

BID

2 % tofacitinib QD

1 % tofacitinib QD

Vehicle

QD

 

N = 71

N = 70

N = 71

N = 70

N = 74

N = 74

Number of AEs

47

51

54

66

65

62

Patients with treatment-emergent AEs, n (%)

30 (42.3)

30 (42.9)

28 (39.4)

34 (48.6)

28 (37.8)

40 (54.1)

Patients with application site AEs, n (%)

4 (5.6)

0 (0.0)

4 (5.6)

8 (11.4)

7 (9.5)

12 (16.2)

Patients with SAEs, n (%)

0 (0.0)

5 (7.1)

2 (2.8)

0 (0.0)

2 (2.7)

1 (1.4)

Patients discontinued due to AEs, n (%)

0 (0.0)

1 (1.4)a

4 (5.6)

6 (8.6)

3 (4.1)

7 (9.5)

Deaths, n (%)

0 (0.0)

1 (1.4)a

0 (0.0)

0 (0.0)

0 (0.0)

0 (0.0)

  1. aPatient had an AE of myocardial infarction and subsequently died; the patient is counted as a discontinuation due to AE and as a death
  2. Categories of adverse events experienced include treatment-emergent, application site and serious adverse events
  3. AE adverse event, BID twice daily, QD once daily, SAE serious adverse event