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. 2023 Sep 21;64:102240. doi: 10.1016/j.eclinm.2023.102240

Table 3.

Treatment-related adverse events in all treated patients (N = 49).

Adverse events All patients Grade 1–2 Grade 3–4
HFS reaction 28 (57) 25 (51) 3 (6)
Cholesterol elevation 23 (47) 23 (47) 0
Proteinuria 21 (43) 21 (43) 0
Triglyceride elevation 20 (41) 19 (39) 1 (2)
Hypertension 19 (39) 14 (29) 5 (10)
TSH elevation 17 (35) 17 (35) 0
Diarrhoea 16 (33) 16 (33) 0
Urine occult blood 15 (31) 15 (31) 0
Faecal occult blood 14 (29) 14 (29) 0
Hypothyroidism 13 (27) 13 (27) 0
Arthralgia 13 (27) 13 (27) 0
Pharyngalgia 10 (20) 10 (20) 0
ALT elevation 9 (18) 9 (18) 0
AST elevation 9 (18) 9 (18) 0
Leukopenia 9 (18) 9 (18) 0
Hyperuricemia 8 (16) 8 (16) 0
Serum creatinine elevation 8 (16) 8 (16) 0
Neutropenia 7 (14) 6 (12) 1 (2)
Voice hoarse 7 (14) 7 (14) 0
Gingivitis 6 (12) 6 (12) 0
Abdominal pain 6 (12) 6 (12) 0
Headache 6 (12) 6 (12) 0
Hyperbilirubinemia 6 (12) 5 (10) 1 (2)
Fatigue 5 (10) 5 (10) 0
Hypokalemia 5 (10) 5 (10) 0
Oral mucositis 5 (10) 5 (10) 0
Dizziness 5 (10) 5 (10) 0
Nausea 5 (10) 5 (10) 0
Thrombocytopenia 5 (10) 5 (10) 0

Data presented as n (%). Each patient is counted once for a specific adverse event. Only the highest grade of a given adverse event is reported for each patient. Listed are events of any grade reported in at least 10% of patients.

HFS = hand-foot skin. TSH = thyroid stimulating hormone. ALT = alanine aminotransferase. AST = aspartate aminotransferase.