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. 2024 Apr 22;8(4):e13069. doi: 10.1002/jgh3.13069

Table 2.

Adverse events based on a questionnaire

Any (score of 1, 2, or 3) VAM triple therapy VAC triple therapy P
Diarrhea 33% 37% 0.82
Dysgeusia 21% 17% 1
Nausea 14% 2% 0.11
Anorexia 23% 5% 0.03
Abdominal pain 23% 23% 1
Heartburn 16% 12% 0.76
Hives 0% 5% 0.49
Headache 16% 16% 1
Abdominal fullness 56% 14% <0.001
Belching 21% 12% 0.38
Vomiting 0% 0% 1
General malaise 16% 9% 0.52
Other 2% 5% 1
Any (score of 2 or 3)
Diarrhea 16% 7% 0.31
Dysgeusia 21% 12% 0.38
Nausea 7% 0% 0.24
Anorexia 9% 0% 0.12
Abdominal pain 7% 2% 0.62
Heartburn 5% 2% 1
Hives 0% 2% 1
Headache 5% 2% 1
Abdominal fullness 28% 2% 0.007
Belching 9% 2% 0.36
Vomiting 0% 0% 1
General malaise 2% 0% 1
Other 0% 0% 1
Score of 3
Diarrhea 5% 5% 1
Dysgeusia 2% 9% 0.36
Nausea 0% 0% 1
Anorexia 2% 0% 1
Abdominal pain 2% 0% 1
Heartburn 0% 0% 1
Hives 0% 2% 1
Headache 2% 2% 1
Abdominal fullness 7% 2% 0.62
Belching 0% 0% 1
Vomiting 0% 0% 1
General malaise 0% 0% 1
Other 0% 0% 1

VAC triple therapy, vonoprazan + amoxicillin + clarithromycin 1‐week eradication therapy; VAM triple therapy: vonoprazan + amoxicillin + metronidazole 1‐week eradication therapy. The bold showes less than 0.05.