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. Author manuscript; available in PMC: 2010 Feb 9.
Published in final edited form as: BJU Int. 2009 Jan 9;103(12):1636. doi: 10.1111/j.1464-410X.2008.08327.x

Table 2.

Treatment-related adverse events (n = 24 patients)

Adverse Events Grade 1 Grade 2 Grade 3 Grade 4
Blood/Bone Marrow
   Anemia 2 1 1
   Thrombocytopenia 2 1
Cardiovascular
   CNS cerebrovascular ischemia 1
   Hypertension 3
   Thrombosis/embolism (vascular access-related) 1 1
Constitutional symptoms
   Fatigue 10 2 2
   Weight loss 3 2
Dermatology/skin
   Hand-foot skin reaction 1 9 3
   Rash/desquamation 11 3 1
Gastrointestinal
   Diarrhea 6 2
   Nausea 1 1 1
Infection 1
Metabolic/Laboratory
   ALT,SGPT 6 2
   AST,SGOT 8 1
   Alkaline phosphatase 1 4 1
   Hyperkalemia 1
   Hyponatremia 1 1
   Hypophosphatemia 3 5
Pain
   Musculoskeletal 3 7
   Throat/larynx 1 1
Pulmonary/Upper respiratory
   Voice changes 3