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Table 2 Summary of Adverse Events Occurring in Patients With and Without Allodynia

From: Effects of onabotulinumtoxinA treatment in patients with and without allodynia: results of the COMPEL study

 

With Allodynia

(n = 290)

Without Allodynia

(n = 426)

AEs, n (%)

  ≥ 1 AE

185 (63.8)

251 (58.9)

 Serious AE

36 (12.4)

39 (9.2)

 Discontinuation due to AE

14 (4.8)

18 (4.2)

TRAEs, n (%)

  ≥ 1 TRAE

56 (19.3)

75 (17.6)

TRAEs occurring in ≥1% of either subgroup

 Neck pain

15 (5.2)

14 (3.3)

 Eyelid ptosis

6 (2.1)

12 (2.8)

 Musculoskeletal stiffness

6 (2.1)

11 (2.6)

 Headache

6 (2.1)

6 (1.4)

 Injection site pain

5 (1.7)

9 (2.1)

 Facial paresis

4 (1.4)

5 (1.2)

 Muscular weakness

3 (1.0)

7 (1.6)

 Migraine

3 (1.0)

4 (0.9)

 Injection site hematoma

3 (1.0)

1 (0.2)

 Muscle spasms

3 (1.0)

1 (0.2)

 Skin tightness

1 (0.3)

6 (1.4)

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