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. 2016 Oct 20;9:373–381. doi: 10.2147/CCID.S115256

Table 3.

Treatment-emergent adverse events by products used

TEAE Soft-L (N=18)
Basic-L (N=72)
Extra/Intense-L (N=86)
Modélis-L (N=6)
Total (N=108)
n % m n % m n % m n % m n % m
Patients with ≥1 TEAE 8 44.4 11 36 50.0 84 41 47.7 114 2 33.3 3 52 48.1 212
Injection-site erythema 4 22.2 4 29 40.3 43 36 41.9 55 0 0.0 0 45 41.7 102
Injection-site swelling 2 11.1 2 20 27.8 29 25 29.1 42 2 33.3 2 36 33.3 75
Injection-site bruising 3 16.7 3 7 9.7 10 7 8.1 10 1 16.7 1 14 13.0 24
Injection-site discoloration 1 5.6 2 2 2.8 2 2 2.3 3 0 0.0 0 3 2.8 7
Injection-site induration 0 0.0 0 0 0.0 0 3 3.5 4 0 0.0 0 3 2.8 4

Note: n, number of patients who experienced ≥1 TEAE; m, number of TEAEs.

Abbreviations: Soft-L, Soft Lidocaine; Basic-L; Basic Lidocaine; Extra/Intense-L, Extra/Intense Lidocaine; Modélis-L, Modélis® Shape Lidocaine; TEAE, treatment-emergent adverse event.