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. 2013 Jun 1;7(6):1120–1124. doi: 10.7860/JCDR/2013/4742.3027

[Table/Fig-5]:

Percentage data of non-hematological adverse events

Adverse event Intaxel Group Taxol Group
CTC Grade CTC Grade
Grade 1 Grade 2 Grade 3 Grade 4 Total Grade 1 Grade 2 Grade 3 Grade 4 Total
Alopecia 2 8 2 3 15 (60%) 1 17 1 2 21 (88%)
Asthenia 2 4 6 (24%) 8 3 11 (46%)
Neurosensory loss 1 1 (4%) 5 3 8 (33%)
Nausea 5 5 (20%) 3 3 6 (25%)
Vomiting 1 1 2 (8%) 3 3 (13%)
Myalgia 1 1 (4%) 2 3 5 (21%)
Pain in limbs 1 1 2 (8%) 1 1 2 (8%)
Diarrhoea 1 1 1 3 (12%) 1 1 (4%)
Cough 1 1 (4%) 1 1 (4%)
Fever - 3 3 (13%)
Loss of appetite - 2 1 3 (13%)
Headache - 2 2 (8%)
Abdominal pain - 1 1 2 (8%)
Motor Neuropathy - 1 1 (4%)
Nail changes - 1 1 (4%)
Hypersensitivity - 1 1 (4%)
Urticaria - 1 1 (4%)
Skin hyperemia - 1 1 (4%)
Flushing 1 1 (4%) -
Nail pain 1 1 (4%) -
Bone pain 1 1 (4%) -
Tachycardia 1 1 (4%) -
Epistaxis 1 1 (4%) -
Epigastric pain 1 1 (4%) -
Somnolence 1 1 (4%) -
Conjunctivitis - 1 1 (4%)
Superficial phlebitis - 1 1 (4%)
Lymphedema - 1 1 (4%)
Aphthous ulcer - 1 1 (4%)
Sacral abscess - 1 1 (4%)
Loss of consciousness - 1 1 (4%)