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. 2024 Jan 5;14:1288159. doi: 10.3389/fphar.2023.1288159

TABLE 6.

Statistic of adverse reaction events.

Adverse reaction events Intervention group (813 patients) Control group (811 patients)
Xerostomia 4(0.49%) 11(1.36%)
Mild headache or dizziness 9(1.11%) 14(1.73%)
Gastrointestinal reactions Mild stomach pain 5(0.62%) 2(0.25%)
Mild nausea 1(0.12%) 4(0.49%)
Abdominal distention 13(1.60%) 2(0.25%)
Diarrhoea 4(0.49%) 1(0.12%)
Total 36(4.43%) 34(4.19%)