Skip to main content
. 2018 Jan 25;17:52. doi: 10.1186/s12936-018-2200-1

Table 4.

Adverse events during the follow-up period

AS–AQ
(N = 221)
DHA–PPQ
(N = 221)
AM–LM
(N = 221)
p
n (%) n (%) n (%)
Fever 90 (40.7) 94 (42.5) 94 (42.5) 0.906
Cough 31 (14.0) 36 (16.3) 22 (10.0) 0.141
Rhinorrhoea 20 (9.1) 27 (12.2) 17 (7.7) 0.255
Diarrhoea 19 (8.6) 14 (6.4) 15 (6.8) 0.624
Conjunctivitis 11 (5.0) 7 (3.2) 15 (6.8) 0.216
Pyoderma 12 (5.4) 6 (2.7) 6 (2.7) 0.211
Vomit 8 (3.6) 6 (2.7) 5 (2.3) 0.684
Anorexia 6 (2.7) 4 (1.8) 1 (0.5) 0.173
Asthenia 1 (0.5) 0 (0.0) 0 (0.0) 0.367
Abdominal pain 3 (1.4) 0 (0.0) 1 (0.5) 0.172
Arthralgia 1 (0.5) 0 (0.0) 0 (0.0) 0.367
Headache 1 (0.5) 0 (0.0) 0 (0.0) 0.367
Convulsions 1 (0.5) 0 (0.0) 0 (0.0) 0.367
Hepatomegaly 0 (0.0) 1 (0.5) 0 (0.0) 0.367
Splenomegaly 1 (0.5) 2 (0.9) 1 (0.5) 0.778
Other events 34 (15.4) 40 (18.1) 45 (20.4) 0.457