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Table 3 Dissolution test results of artemether–lumefantrine samples (N = 74) collected from low and high malaria transmission settings in Uganda, June–December 2021

From: Pharmacopeial quality of artemether–lumefantrine anti-malarial agents in Uganda

Brand name

Artemether label claim (mg)

Number of samples tested

n (%)

Artemether within pharmacopeial limit, 70%

Pass/Fail

Lumefantrine within pharmacopeial limit, 60%

Pass/Fail

LONART

20/120

20 (27%)

Pass

Pass

40/240

1 (1.4%)

Pass

Pass

80/480

3 (4.1%)

Pass

Pass

LONART-DS

80/480

1 (1.4%)

Pass

Pass

ARTEFAN

20/120

12 (16.2%)

Pass

Pass

40/240

1 (1.4%)

Pass

Pass

60/360

1(1.4%)

Pass

Pass

80/480

1(1.4%)

Pass

Pass

LUMARTEM

20/120

2 (2.7%)

Pass

Pass

80/480

1 (1.4%)

Pass

Pass

CO-METHER

20/120

5 (6.8%)

Pass

Pass

KOMEFAN-140

20/120

1 (1.4%)

Pass

Pass

COMBIART

20/120

5 (6.8%)

Pass

Pass

LUMERAX

20/120

1 (1.4%)

Pass

Pass

LARIACT

20/120

3 (4.1%)

Pass

Pass

Cach-ART

20/120

2 (2.7%)

Pass

Pass

LUMAREN

20/120

2 (2.7%)

Pass

Pass

COARTEM

20/120

1 (1.4%)

Pass

Pass

KOMEFAN

20/120

1 (1.4%)

Pass

Pass

LUMITER

20/120

6 (8.1%)

Pass

Pass

Not Indicateda

20/120

4 (5.4%)

Pass

Pass

Total number

74 (100%)

74 (100%)

74(100%)

  1. aOne batch of samples with not brand name indicate (HWE111219) from a low malaria transmission setting had 68% artemether dissolution