Table 1.

AEs reported in at least 2 patients

All cohorts (N = 18)
Total patients with ≥1 AE, n (%) 18 (100.0) 
Total number of AEs 150 
AEs reported in ≥2 patients, n (%)  
 Nasopharyngitis 8 (44.4) 
 Contusion 7 (38.9) 
 Dental caries 6 (33.3) 
 Pharyngitis 5 (27.8) 
 Headache 5 (27.8) 
 Excoriation 4 (22.2) 
 Upper respiratory tract infection 3 (16.7) 
 Tongue injury 3 (16.7) 
 Wound 3 (16.7) 
 Diarrhea 3 (16.7) 
 Injection-site erythema 3 (16.7) 
 Injection-site hematoma 3 (16.7) 
 Injection-site pruritus 3 (16.7) 
 Erythema 3 (16.7) 
 Myalgia 3 (16.7) 
 Infected dermal cyst 2 (11.1) 
 Nausea 2 (11.1) 
 Malaise 2 (11.1) 
 Dizziness 2 (11.1) 
 Back pain 2 (11.1) 
 Rhinitis allergic 2 (11.1) 
 Hemophilia 2 (11.1)* 
 Calculus ureteric 2 (11.1) 
All cohorts (N = 18)
Total patients with ≥1 AE, n (%) 18 (100.0) 
Total number of AEs 150 
AEs reported in ≥2 patients, n (%)  
 Nasopharyngitis 8 (44.4) 
 Contusion 7 (38.9) 
 Dental caries 6 (33.3) 
 Pharyngitis 5 (27.8) 
 Headache 5 (27.8) 
 Excoriation 4 (22.2) 
 Upper respiratory tract infection 3 (16.7) 
 Tongue injury 3 (16.7) 
 Wound 3 (16.7) 
 Diarrhea 3 (16.7) 
 Injection-site erythema 3 (16.7) 
 Injection-site hematoma 3 (16.7) 
 Injection-site pruritus 3 (16.7) 
 Erythema 3 (16.7) 
 Myalgia 3 (16.7) 
 Infected dermal cyst 2 (11.1) 
 Nausea 2 (11.1) 
 Malaise 2 (11.1) 
 Dizziness 2 (11.1) 
 Back pain 2 (11.1) 
 Rhinitis allergic 2 (11.1) 
 Hemophilia 2 (11.1)* 
 Calculus ureteric 2 (11.1) 

All data collected after dose up-titrations were included.

*

Serious adverse event (SAE; left hip joint bleeding and subcutaneous hemorrhage of the proglossis).

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