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. 2024 Jun 3;15:1414268. doi: 10.3389/fphar.2024.1414268

TABLE 1.

Clinical characteristics of patients with adverse events under different administration routes of Semaglutide

Characteristics Subcutaneous of semaglutide Oral of semagluti
X Overall Overall
(N = 16,346) (N = 2,496)
SEX,n (%)
F 10,311 (63.1%) 1,409 (56.5%)
M 5,342 (32.7%) 1,002 (40.1%)
Missing 693 (4.2%) 85 (3.4%)
WT (kg),n (%)
<50 11 (0.1%) 18 (0.7%)
>100 635 (3.9%) 93 (3.7%)
50–100 1,055 (6.5%) 238 (9.5%)
Missing 14,645 (89.6%) 2,147 (86.0%)
AGE (year),n (%)
<18 11 (0.1%) 1 (0.0%)
>85 57 (0.3%) 36 (1.4%)
18–64.9 4,615 (28.2%) 650 (26.0%)
65–85 3,395 (20.8%) 556 (22.3%)
Missing 8,268 (50.6%) 1,253 (50.2%)
COUNTRY,n (%)
US 15,286 (93.5%) 2045 (81.9%)
CN 66 (0.4%) 1 (0.0%)
CA 185 (1.1%) 5 (0.2%)
GB 82 (0.5%) 27 (1.1%)
DK 102 (0.6%) 21 (0.8%)
JP 111 (0.7%) 262 (10.5%)
Reporting year,n (%)
2023 5,841 (36%) 729 (29%)
2022 3,954 (24%) 707 (28%)
2021 2,485 (15%) 646 (26%)
2020 2019 (12%) 412 (17%)
2019 1,037 (6%) 2 (0%)
2018 1,010 (6%)
Outcome,n (%)
HO 1778 (10.5%) 390 (14.8%)
DE 108 (0.6%) 43 (1.6%)
DS 191 (1.1%) 39 (1.5%)
LT 124 (0.7%) 29 (1.1%)
CA 2 (0.0%) 1 (0.0%)
RI 67 (0.4%) 10 (0.4%)
OT 3,432 (20.3%) 577 (21.9%)
Missing 11,245 (66.4%) 1,546 (58.7%)

Note: n, number of cases with available.