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. 2009 Sep 28;4(9):e7164. doi: 10.1371/journal.pone.0007164

Table 4. Incidence of solicited adverse events reported by mother or carer four days day after the first administration of IPT.

SP-AQ (N = 694) DHA-PQ (N = 559) SP-PQ (N = 454)
Vomitted 218 (31%) 76 (14%) 76 (17%)
<24 months 26% (74/282) 17% (36/210) 21% (42/196)
Risk difference (95%CI) Reference −8.4 (−18, 1.6) −5.6 (−16, 5)
≥24 months 35% (144/412) 12% (40/348) 13% (34/258)
Risk difference (95%CI) Reference −22.7 (−32, −14) −22.1 (−32, −13)
Fever 219 (32%) 98 (18%) 89 (20%)
<24 months 28% (79/282) 20% (42/210) 19% (37/196)
Risk difference (95%CI) Reference −5.9 (−16.5, 4.7) −8.3 (−19.6, 3)
≥24 months 34% (140/412) 16% (56/348) 20% (52/258)
Risk difference (95%CI) Reference −17 (−28, −5.5) −13 (−25, −1.1)
Rash 14 (2%) 3 (0.5%) 5 (1.1%)
Risk difference (95%CI) Reference −1.2 (−3.1, 0.6) −0.8 (−2.8, 1.1)
Itching 27 (3.9%) 7 (1.3%) 8 (1.8%)
Risk difference (95%CI) Reference −2.7 (−5.5, 0.1) −2.4 (−5.4, 0.6)
Headache 87 (13%) 32 (5.7%) 18 (4%)
Risk difference (95%CI) Reference −6.7 (−13.2, −0.1) −8.7 (−15.6, −1.7)

Intraclass correlation coefficients for each outcome were as follows: vomiting 0.067, fever 0.078, rash 0.024, itching 0.039, headache 0.072. Risk differences were adjusted for age, or presented stratified by age group when there was a signification interaction with age.