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. Author manuscript; available in PMC: 2016 Jul 1.
Published in final edited form as: Cancer. 2015 Apr 6;121(13):2156–2163. doi: 10.1002/cncr.29337

Table 3b.

b. Adverse events ≥ grade 3 occurring >90 days but ≤365 from the start of concurrent treatment (late)

System Organ Class Term Grade Relationship to Treatment Days from Concurrent RX start
General disorders and administration site conditions Fatigue 3 Probable 105

Metabolism and nutrition disorders Hypomagnesemia 4 Possible 183
Hypokalemia 3 Possible 168

Respiratory, thoracic and mediastinal disorders Epistaxis* 3 Probable 176

Nervous system disorders Headache 3 Probable 98

Metabolism and nutrition disorders Hyponatremia 3 Possible 98

Vascular disorders Hot flashes 3 Definite 300

General disorders and administration site conditions Pain 3 Possible 180

Ear and labyrinth disorders Hearing impaired 3 Probable 333

Metabolism and nutrition disorders Hypokalemia 4 Probable 136
Nervous system disorders Neuralgia 3 Possible 126
Infections and infestations Skin infection 3 Possible 126
*

probably attributable to bevacizumab

Key: RX=treatment