Table 2

Most common adverse events related to study treatment that occurred in 5% or more of patients in either treatment group during period 1

Plerixafor (n = 147)Placebo (n = 151)
Any related adverse events, n (%) 95 (64.6) 67 (44.4) 
Gastrointestinal disorders   
    Diarrhea 27 (18.4) 8 (5.3) 
    Nausea 24 (16.3) 11 (7.3) 
    Vomiting 8 (5.4) 4 (2.7) 
General disorders and administration site conditions   
    Fatigue 12 (8.2) 5 (3.3) 
    Injection site erythema 30 (20.4) 5 (3.3) 
Musculoskeletal and connective tissue disorders   
    Bone pain 14 (9.5) 12 (7.9) 
Nervous system disorders   
    Headache 8 (5.4) 13 (8.6) 
    Paresthesia 11 (7.5) 11 (7.3) 
Plerixafor (n = 147)Placebo (n = 151)
Any related adverse events, n (%) 95 (64.6) 67 (44.4) 
Gastrointestinal disorders   
    Diarrhea 27 (18.4) 8 (5.3) 
    Nausea 24 (16.3) 11 (7.3) 
    Vomiting 8 (5.4) 4 (2.7) 
General disorders and administration site conditions   
    Fatigue 12 (8.2) 5 (3.3) 
    Injection site erythema 30 (20.4) 5 (3.3) 
Musculoskeletal and connective tissue disorders   
    Bone pain 14 (9.5) 12 (7.9) 
Nervous system disorders   
    Headache 8 (5.4) 13 (8.6) 
    Paresthesia 11 (7.5) 11 (7.3) 

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