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Table 2 Summary of Adverse Events in Patients With and Without Daily Headache

From: Effects of onabotulinumtoxinA treatment in chronic migraine patients with and without daily headache at baseline: results from the COMPEL Study

AE, n (%)

With Daily Headache (n = 138)

Without Daily Headache (n = 504)

≥1 AE

99 (71.7)

297 (58.9)

Serious AE

20 (14.5)

44 (8.7)

Study discontinuation due to AE

10 (7.2)

17 (3.4)

≥1 TRAE

24 (17.4)

97 (19.2)

Individual TRAEs occurring in ≥1% of any subgroup

 Neck pain

5 (3.6)

23 (4.6)

 Eyelid ptosis

3 (2.2)

14 (2.8)

 Musculoskeletal stiffness

4 (2.9)

13 (2.6)

 Injection site pain

3 (2.2)

11 (2.2)

 Headache

2 (1.4)

8 (1.6)

 Muscular weakness

1 (0.7)

9 (1.8)

 Facial paresis

1 (0.7)

6 (1.2)

 Migraine

0 (0.0)

6 (1.2)

 Skin tightness

1 (0.7)

5 (1.0)

 Influenza-like illness

2 (1.4)

1 (0.2)

 Balance disorder

2 (1.4)

0 (0.0)

 Dizziness

3 (2.2)

0 (0.0)

  1. AE adverse event, TRAE treatment-related adverse event