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. 2017 Apr 25;116(11):1402–1407. doi: 10.1038/bjc.2017.119

Table 2. Treatment-related adverse events occurring in two or more participants, and all grade 3/4 treatment-related adverse events.

  Grades 1–2
Grades 3–4
Event No. of patients % No. of patients %
Cardiorenal
Oedema, facial 3 12    
Oedema, limbs 4 16    
Elevated creatinine 2 8    
Hypertension 16 64 2 8
Hypomagnesaemia 7 28    
Hyponatraemia 2 8    
Proteinuria 3 12    
Constitutional
Dehydration 2 8    
Fatigue 15 60 1 4
Dermatologic
Dry skin 3 12    
Finger or nail changes 3 12    
Rash 20 80 3 12
Gastrointestinal
Anorexia 9 36    
Constipation 3 12    
Diarrhoea 13 52 1 4
Elevated liver function tests 8 32 3 12
Mucositis 2 8    
Nausea or vomiting 16 64 2 8
HEENT
Blurry vision 5 20    
Change in taste 6 24    
Congestion or postnasal drip 2 8    
Floaters 2 8    
Haematologic
Anaemia 3 12 1 4
Bleeding or bruising 7 28    
Neutropenia 3 12    
Thrombocytopenia 10 40 6 24
Neurological
Amnesia 1 4 1 4
Dizziness 2 8    
Dysgeusia 2 8    
Headache 2 8    
Posterior reversible encephalopathy syndrome (PRES) 1 4 1 4

Abbreviation: HEENT=head, eyes, ears, nose, and throat.