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. 2013 Jul 11;12:236. doi: 10.1186/1475-2875-12-236

Table 1.

Adverse drug reactions reported through active and passive surveillance and dominant symptoms reported

  Rufiji District Kilombero/Ulanga Districts1 Total (%)
Total suspected adverse drug events reported
45
50
95 (100)
Identified through active surveillance
21
30
51 (53.7)
Identified through passive surveillance
24
20
44 (46.3)
Number of cases successfully traced
38
41
79 (83.2)
Of the successfully traced cases:
38
41
N = 79 (100)
Events associated with SP monotherapy
20
33
53 (67.1)
Events associated with AS/SP combination therapy
13
0
13 (16.5)
Events associated with AS monotherapy
1
0
1 (1.3)
Events outside DSS area (excluded)
3
5
8 (10.0)
Events unrelated to SP and/or AS (excluded)
1
3
4 (5.0)
Dominant symptoms reported for those included:
34
33
N = 67 (100)
Body blisters and skin detachment
7
11
18 (26.9)
Body swelling, itching and urticarial rashes
10
6
16 (23.9)
Multiple lésions on mucus membranes
6
7
13 (19.4)
Facial edema, sore mouth/nose conjunctiva
5
4
9 (13.4)
Others1
6
5
11 (16.4)
Deaths
Deaths attributable to SP and/or AS caused ADR 2 4 6 (8.9%)

1. These include side effects such as headache, lightheadedness, shortness of breath, stomachache, diarrhoea, vomiting and kidney pain.