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. 2023 May 17;15(5):342. doi: 10.3390/toxins15050342

Table 2.

Dosing regimen and subject characteristics by onabotulinumtoxinA indication.

Indication Subjects, n Gender (M, F),
n (%)
Maximum No. of Treatment Cycles Mean (SD) No. of Treatment Cycles Dose Range, U Mean (SD) Dose, U Dosing Route
Cervical dystonia 326 98 (30), 228 (70) 15 8.4 (3.22) 20–500 187.3 (76.47) IM
Glabellar lines 846 100 (12), 746 (88) 5 2.8 (1.15) 10–20 17.2 (4.51) IM
Hyperhidrosis 1077 439 (41), 638 (59) 14 2.8 (1.97) 100–150 102.8 (11.41) ID
Migraine 501 69 (14), 432 (86) 3 2.8 (0.53) 75–260 165.2 (57.00) IM
Adult post-stroke spasticity 449 224 (50), 225 (50) 5 3.3 (1.42) 100–600 307.3 (79.18) IM
NDO 619 256 (41), 363 (59) 13 3.1 (2.28) 200–300 238.2 (48.59) IM
Lateral canthal lines 916 109 (12), 807 (88) 4 2.5 (1.19) 24–44 33.8 (10.00) IM
Overactive bladder a 974 108, (11), 866 (89) 13 3.6 (2.48) 20–200 108.7 (19.26) IM
Pediatric lower limb spasticity 325 173 (53), 152 (47) 6 4.2 (1.37) 40–340.5 177.7 (76.23) IM
Pediatric NDO 113 65 (58), 48 (42) 4 2.4 (0.92) 50–200 128.4 (59.85) IM
Total 6146 M: 1641 (27),
F: 4505 (73)
3–15 3.3 (2.25) 10–600 134.8 (94.89) ID, IM

Indications are ordered by year of onabotulinumtoxinA US Food and Drug Administration approval (see Figure 1 for approval years). Abbreviations—F, female; ID, intradermal; IM, intramuscular; M, male; and NDO, neurogenic detrusor overactivity. a Excludes neurogenic causes, which are instead included in NDO.