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. 2022 Mar 12;21:84. doi: 10.1186/s12936-022-04100-1

Table 5.

Adverse events reported during follow-up

Adverse effect Overall CYP2D6 Test, p-value G6PD Test, p-value
Reduced Normal Deficient Normal
Mild urine colour change, n (%) 79 (63.7) 17 (51.5) 62 (50.0) 1.861, 0.394 12 (60.0) 58 (50.0) 1.408, 0.843
Haemoglobinuria, n (%) 14 (11.3) 1 (3.0) 13 (10.5) 1.861, 0.394 1 (5.0) 11 (9.5) 1.408, 0.843
Abdominal pain, n (%) 9 (7.3) 0 (0) 9 (7.3) 2.541, 0.206 2 (10.0) 4 (3.4) 4.637, 0.098
Diarrhoea, n (%) 9 (7.3) 1 (3.0) 8 (6.5) 0.565, 0.686 1 (5.0) 7 (6.0) 0.076, 0.963
Vomiting, n (%) 5 (4.0) 1 (3.0) 4 (3.2) 0.003, 1.0 2 (10.0) 3 (2.6) 3.838, 0.147
Nausea, n (%) 4 (3.2) 1 (3.0) 3 (2.4) 0.039, 1.0 2 (10.0) 2 (1.7) 5.339, 0.069
Dizziness, n (%) 2 (1.6) 0 (0) 2 (1.6) 0.539, 1.0 0 (0) 2 (1.7) 0.716, 0.699
Coughing, n (%) 1 (0.8) 0 (0) 1 (0.8) 0.268, 1.0 0 (0) 1 (0.9) 0.356, 0.837
Rashes, n (%) 1 (0.8) 0 (0) 1 (0.8) 0.268, 1.0 0 (0) 1 (0.9) 0.356, 0.837