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. 2013 Jul 10;2013:961926. doi: 10.1155/2013/961926

Table 5.

Adverse events in patients reported in the two groups during treatment.

Variable Treatment group
Number of patients (%)
(n = 200)
Control group
Number of patients (%)
(n = 100)
χ 2 (Chi-square test) P values
Abdominal pain 9 (4.5) 3 (3) 0.3906 0.5320
Abdominal distension 15 (7.5) 2 (2) 3.7726 0.0521
Diarrhea 14 (7) 3 (3) 1.9954 0.1578
Nausea 5 (2.5) 2 (2) 0.0000 1.0000
Increased appetite 34 (17) 1 (1) 16.5606 0.0000
Appetite decreases 5 (2.5) 4 (4) 0.1289 0.7196
Feel thirsty 4 (2) 3 (3) 0.0183 0.8924
Stomach disturbances 19 (9.5) 5 (5) 1.8342 0.1756
Constipation 4 (2) 3 (3) 0.0183 0.8924
Malaise 5 (2.5) 2 (2) 0.0000 1.0000
Insomnia 3 (1.5) 1 (1) 0.0000 1.0000
Headache 3 (1.5) 2 (2) 0.0000 1.0000
Dizziness 5 (2.5) 1 (1) 0.1913 0.6618
Fatigue 3 (1.5) 2 (2) 0.0000 1.0000
Chest tightness 4 (2) 3 (3) 0.0183 0.8924
URTI syndromes 3 (1.5) 3 (3) 0.1913 0.6618
Mouth ulceration 3 (1.5) 2 (2) 0.0000 1.0000
Rash 5 (2.5) 0 (0) 1.2458 0.2644
Dysuria 2 (1) 0 (0) 0.0629 0.8019
Urethral burning pain 2 (1) 0 (0) 0.0629 0.8019
Increased serum ALT 3 (1.5) 0 (0) 0.3788 0.5383

URTI: upper respiratory tract infection; increased serum ALT defined as >40 U/L.

Correction.