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. 2016 Dec 29;107(12):1843–1850. doi: 10.1111/cas.13098

Table 2.

Grade 3 and 4 adverse events

Adverse event FOLFIRI plus panitumumab (n = 61) FOLFIRI plus bevacizumab (n = 60)
≥Grade 3 ≥Grade 3
n % n %
Any adverse events 54 88.5 40 66.7
Neutropenia 30 49.2 28 46.7
Stomatitis 13 21.3 4 6.7
Leucopenia 11 18.0 17 28.3
Acneiform rash 10 16.4 0 0.0
Hypomagnesemia 7 11.5 0 0.0
Anorexia 6 9.8 7 11.7
Proteinuria 6 9.8 2 3.3
Non‐neutropenic infection 5 8.2 3 5.0
Dry skin 5 8.2 0 0.0
Paronychia 4 6.6 0 0.0
Thromboembolic events 4 6.6 0 0.0
Anemia 3 4.9 7 11.7
Diarrhea 3 4.9 4 6.7
Nausea 2 3.3 3 5.0
Vomiting 2 3.3 3 5.0
Febrile neutropenia 2 3.3 3 5.0
Fatigue 1 1.6 5 8.3
Thrombocytopenia 1 1.6 3 5.0
Any bleeding 1 1.6 2 3.3
Pneumonitis 1 1.6 1 1.7
Gastrointestinal perforation 0 0.0 1 1.7

FOLFIRI, fluorouracil, leucovorin, and irinotecan.