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. 2014 Oct 29;100(1):E77–E81. doi: 10.1210/jc.2014-2246

Table 1.

Adverse Events by CTCAE Version 4 Classification in 17 Patients Treated with Vemurafenib

Adverse event All grades N (%) Grade 1 N (%) Grade 2 N (%) Grade 3 N (%) Grade 4 N (%)
Overall (at least one AE) 17 (100) 15 (88) 16 (94) 7 (41) 1 (6)
Fatigue 12 (71) 9 (53) 2 (12) 1 (6) -
Weight loss 12 (71) 8 (47) 4 (24) - -
Anorexia 11 (65) 5 (29) 6 (35) - -
Arthralgias 10 (59) 5 (29) 5 (29) - -
Hair loss 10 (59) 9 (53) 1 (6) - -
Rash 10 (59) 5 (29) 5 (29) - -
Hand-foot syndrome 9 (53) 5 (29) 3 (18) 1 (6) -
Calluses 8 (47) 8 (47) - - -
Diarrhea 8 (47) 6 (35) 2 (12) - -
Fever 7 (41) 7 (41) - - -
Dry mouth 6 (35) 4 (24) 2 (12) - -
Nausea 6 (35) 5 (29) 1 (6) - -
Verrucous keratosis 6 (35) - 6 (35) - -
Photosensitivity 4 (24) 1 (6) 2 (12) 1 (6) -
Mucositis 3 (18) 2 (12) 1 (6) - -
Weakness 3 (18) 2 (12) 1 (6) - -
Squamous cell skin carcinoma 3 (18) - - 3 (18) -
Blurry vision 2 (12) 2 (12) - - -
Dysgeusia 2 (12) - 2 (12) - -
Hoarseness 2 (12) 2 (12) - - -
HTN 2 (12) 1 (6) 1 (6) - -
Vomiting 2 (12) 2 (12) - - -
Constipation 1 (6) 1 (6) - - -
Headache 1 (6) 1 (6) - - -
Nail changes 1 (6) 1 (6) - - -
Palmar warts 1 (6) 1 (6) - - -
QT prolongation 1 (6) 1 (6) - - -
Melanocytic nevi 1 (6) - 1 (6) - -
Atrial fibrillation 1 (6) - 1 (6) - -
Gum lesion 1 (6) - 1 (6) - -
Uveitis 1 (6) - - 1 (6) -
Elevated serum lipase 1 (6) - - - 1 (6)

Abbreviations: HTN, hypertension; -, not observed.