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. 2017 Mar 16;8(38):64471–64480. doi: 10.18632/oncotarget.16293

Table 2. Adverse events in the Apatinib treatment.

Adverse event Grade 1* (n, %) Grade 2 (n, %) Grade 3 (n, %) Total
Neutropenia 2(12.5) 1(6.3) - 3(18.8)
Thrombocytopenia 2(12.5) - - 2(12.5)
Bilirubin increased 2(12.5) 1(6.3) - 3(18.8)
Transaminase increased 1(6.3) 1(6.3) - 2(12.5)
Hematuria 1(6.3) - - 1(6.3)
Proteinuria 2(12.5) 4(25.0) 1(6.3) 7(43.8)
Hypertension 1(6.3) 1(6.3) 3(18.7) 5(31.3)
Hand-foot syndrome 1(6.3) 4(25.0) 2(12.5) 7(43.8)
Pain 2(12.5) 2(12.5) - 4(25.0)
Fatigue 1(6.3) 1(6.3) - 2(12.5)
Mucositis - 2(12.5) - 2(12.5)
Anorexia - 1(6.3) - 1(6.3)
Dizziness 1(6.3) - - 1(6.3)
Fever 1(6.3) - - 1(6.3)
Diarrhea 1(6.3) - - 1(6.3)