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. 2021 Oct 28;11:721764. doi: 10.3389/fonc.2021.721764

Table 4.

Adverse events.

Adverse events (n, %) All patients (n = 35) rhTPO group (n = 20) Non-rhTPO group (n = 15) p-value
Infection rate 4 (11.4%) 2 (10.0%) 2 (13.3%) 0.980
Drug-related liver injury 5 (14.3%) 3 (15.0%) 2 (13.3%) 0.991
Drug-related renal injury 2 (5.7%) 1 (5.0%) 1 (6.7%) 0.979
Fatigue 3 (8.6%) 2 (10.0%) 1 (6.7%) 0.809
Gastrointestinal disorders (diarrhea, nausea, and abdominal pain) 7 (20.0%) 4 (20.0%) 3 (20%) 1.000
Intracranial hemorrhage 1 (2.6%) 1 (5.0%) 0 (0%) 0.999

rhTPO, recombinant human thrombopoietin.