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. 2022 May 25;8(6):e09538. doi: 10.1016/j.heliyon.2022.e09538

Table 5.

Adverse events of lenvatinib monotherapy (n = 90).

AEs∗ Not happened Grade 1 Grade 2 Grade 3 Grade 4 happened Any grade
hypertension 56 (62.22) 18 12 4 0 34 (37.78) 4 (4.44)
HFSR 73 (81.11) 11 5 1 0 17 (18.89) 1 (1.11)
Asthenia 60 (66.67) 17 13 0 0 30 (33.33) 0 (0.00)
diarrhoea 66 (73.33) 11 12 1 0 24 (26.67) 1 (1.11)
Constipation 77 (85.56) 10 3 0 0 13 (14.44) 0 (0.00)
Abdominal pain 69 (76.67) 15 6 0 0 21 (23.33) 0 (0.00)
Bloating 72 (80.00) 11 7 0 0 18 (20.00) 0 (0.00)
Nausea 69 (76.67) 17 4 0 0 21 (23.33) 0 (0.00)
Vomiting 75 (83.33) 8 7 0 0 15 (16.67) 0 (0.00)
Loss of appetite 68 (75.56) 14 8 0 0 22 (24.44) 0 (0.00)
OM 85 (94.44) 5 0 0 0 5 (5.56) 0 (0.00)
Joint pain 74 (82.22) 15 1 0 0 16 (17.78) 0 (0.00)
peripheral edema 82 (91.11) 8 0 0 0 8 (8.89) 0 (0.00)
Proteinuria 67 (74.44) 18 5 0 0 23 (25.56) 0 (0.00)
Leukopenia 80 (88.89) 7 2 1 0 10 (11.11) 1 (1.11)
Thrombocytopenia 83 (92.22) 6 1 0 0 7 (7.78) 0 (0.00)

Data are presented as n (%); ∗ counting overlapping; oral mucositis (OM); hand-foot skin reaction (HFSR).