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Table 2 Adverse events reported by treatment

From: Therapeutic efficacy and artemisinin resistance in northern Myanmar: evidence from in vivo and molecular marker studies

 

Total (n = 470)

Artemether + lumefantrine (n = 204)

Artesunate + mefloquine (n = 119)

Dihydroartemisinin + piperaquine (n = 147)

n (%)

n (%)

n (%)

n (%)

Number of adverse events per patient

 0

345 (73)

150 (74)

80 (67)

115 (78)

 1

60 (13)

25 (12)

16 (13)

19 (13)

 2

64 (14)

29 (14)

22 (19)

13 (9)

 3

1 (<1)

0

1 (<1)

0

Most frequent type of adverse event reported

 Dizziness

30 (6.4)

19 (9.3)

9 (7.6)

2 (1.4)

 Nausea

29 (6.2)

13 (6.4)

8 (6.7)

8 (5.4)

 Vomiting

27 (5.7)

8 (3.9)

9 (7.6)

10 (6.8)

 Loss of appetite

19 (4.0)

9 (4.4)

3 (2.5)

7 (4.8)

 Insomnia

15 (3.2)

2 (1.0)

13 (10.9)

0

 Palpitation

14 (3.0)

11 (5.4)

2 (1.7)

1 (0.7)

 Diarrhoea

13 (2.8)

3 (1.5)

3 (2.5)

7 (4.8)

 Abdominal pain

10 (2.1)

3 (1.5)

7 (5.9)

0

 Asthaenia

10 (2.1)

1 (0.5)

4 (3.4)

5 (3.4)

 Headache

6 (1.3)

6 (2.9)

0

0

 Cough

6 (1.3)

2 (1.0)

0

4 (2.7)

 Joint/muscle pain

5 (1.1)

3 (1.5)

1 (0.8)

1 (0.7)

 Skin rash

3 (0.6)

2 (1.0)

1 (0.8)

0

 Nightmare

2 (0.4)

0

2 (1.7)

0