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. 2017 Jan 28;23(4):668–675. doi: 10.3748/wjg.v23.i4.668

Table 3.

Adverse events in first- and second-line eradication therapies n (%)

First-line eradication therapy
Second-line eradication therapy
VPZ EPZ RPZ LPZ VPZ EPZ RPZ LPZ
Adverse events 61 (11.2) 39 (7.7) 9 (10.1) 12 (5.7) 6 (7.9) 14 (13.5) 3 (12.5) 7 (12.3)
Diarrhoea/soft stool 29 (47.5) 25 (64.1) 5 (55.6) 8 (66.7) 4 (66.7) 6 (43.0) 3 (100) 5 (71.4)
Eruption 7 (11.5) 3 (7.7) 2 (22.2) 2 (16.7) 0 3 (21.4) 0 0
Constipation 6 (10.0) 3 (7.7) 0 0
Dysgeusia 3 (5.0) 3 (7.7) 1 (11.1) 0 0 1 (7.1) 0 1 (14.3)
Nausea and vomiting 2 (3.3) 2 (5.1) 0 1 (8.3) 0 1 (7.1) 0 0
Abdominal pain 5 (8.2) 2 (5.1) 0 0 1 (16.7) 2 (14.3) 0 0
Appetite loss 3 (5.0) 0 0 0
General fatigue 2 (3.3) 1 (2.6) 0 0 1 (16.7) 0 0 0
Heartburn 1 (1.6) 0 0 1 (8.3)
Headache 1 (1.6) 0 0 0 0 0 0 1 (14.3)
Fever 1 (1.6) 0 0 0
Flatulence 0 0 1 (11.1) 0
Haematuria 1 (1.6) 0 0 0
Vertigo 0 1 (7.1) 0 0

VPZ: Vonoprazan group; EPZ: Esomeprazole group; RPZ: Rabeprazole group; LPZ: Lansoprazole group.