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. 2017 Jun 19;108(8):1628–1633. doi: 10.1111/cas.13285

Table 3.

Treatment‐emergent, treatment‐related adverse events in ≥3 patients

N = 13 Treatment‐emergent, treatment‐related adverse events
All grades n (%) Grade 3 n (%)
Any adverse event 9 (69.2) 1 (7.7)a
Dysgeusia 9 (69.2) 0
Muscle spasms 5 (38.5) 0
Alopecia 4 (30.8) 0
Decreased appetite 4 (30.8) 0
Blood creatinine phosphokinase increased 3 (23.1) 0
Constipation 3 (23.1) 0
Diarrhea 3 (23.1) 0

No grade 4 or 5 treatment‐related adverse events were reported in this study.

a

One patient experienced grade 3 treatment‐related pyrexia.