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. 2017 Oct 3;9:595–607. doi: 10.2147/CEOR.S146280

Table S1.

Adverse events for patients receiving IFN-based therapy (n=30)

Adverse events (per patient), mean ± SD
14.4±3.76
Adverse events requiring medical treatment (per patient), mean ± SD
2.2±2.16

Common adverse event Patients, n (%) Requiring medical treatment, n (%)a
Fatigue 24 (80) 0
Rash 22 (73.3) 13 (59.1)
Mood change 22 (73.3) 3 (13.6)
 Depression 9 (30) 2 (22.2)
 Irritability 16 (53.3) 1 (6.25)
Pruritus 18 (60) 0
Upper respiratory tract symptoms 16 (53.3) 4 (25)
Weight loss 15 (50) 0
Headache 14 (46.7) 0
Sleep disturbance 12 (40) 5 (41.7)
Flu-like symptoms (non-specific) 12 (40) 0
Myalgia 11 (36.7) 0
Severe hematological adverse event
Hemoglobin
 Hb 80–99 (gL−1) 9 (30) 1 (11.1)
 Hb <80 (gL−1) 1 (3.3) 0
Neutrophils
 0.5–0.99 (×109 L−1) 17 (56.6) 0
 <0.5 (×109 L−1) 3 (10) 0
Platelets
 50–99 (×109 L−1) 12 (40) 0
 <50 (×109 L−1) 2 (6.7) 1 (50)
Serious adverse events (requiring hospital admission) 2 (6.7) 2 (100)
 Immune thrombocytopenic purpura 1 (3.3) 1 (100)
 Osteomyelitis 1 (3.3) 1 (100)

Note:

a

Percentage of total number of patients who experienced the adverse event.

Abbreviations: Hb, hemoglobin; IFN, interferon.