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. 2020 Jan 8;69(6):1019–1026. doi: 10.1136/gutjnl-2019-319954

Table 3.

Adverse events in each therapy group

Adverse event VA-dual
(n=168)
VAC-triple
(n=167)
P value
Diarrhoea 16 (9.5%) 25 (15.0%) 0.128
 Moderate 1 3
Bloating 20 (11.9%) 14 (8.4%) 0.286
 Moderate 1 0
Constipation 10 (6.0%) 8 (4.8%) 0.637
Skin rash 9 (5.4%) 5 (3.0%) 0.280
 Moderate 4 1
Nausea 5 (3.0%) 4 (2.4%) 0.742
 Moderate 0 1
Abdominal pain 6 (3.6%) 2 (1.2%) 0.155
 Moderate 1 0
Dysgeusia 3 (1.8%) 3 (1.8%) 0.994
Oral mucositis 0 6 (3.6%) 0.013
Others 2 (1.2%) 2 (1.2%) 0.995
Total patients 46 (27.4%) 51 (30.5%) 0.524

VAC-triple, vonoprazan, amoxicillin and clarithromycin triple therapy; VA-dual, vonoprazan and amoxicillin dual therapy.