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. 2023 Aug 10;14:1164898. doi: 10.3389/fphar.2023.1164898

TABLE 4.

Adverse events reported in each group.

Classification of adverse events Adverse events Treatment group Control group
Digestive system problem (19 cases) Nausea or vomiting 1 0
Anorexia 4 9
Mild constipation 1 0
Diarrhea 0 2
Skin problem (one case) Pruritus 0 1
“Not otherwise classified” problem (one case) LFT abnormality 0 1
Total number of participants who had an adverse event (21 cases) 6 15

LFT, liver function test.