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Table 2 Assay 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 (%)

Number of samples with artemether content outside pharmacopeiala

range (90–110%)

n (%)

Number of samples with lumefantrine content outside pharmacopeiala

range (90–110%)

n (%)

LONART

20/120

20 (27%)

4 (5.4%)

2 (2.7%)

40/240

1 (1.4%)

0

0

80/480

3 (4.1%)

0

0

LONART-DS

80/480

1 (1.4%)

0

0

ARTEFAN

20/120

12 (16.2%)

0

0

40/240

1 (1.4%)

0

0

60/360

1(1.4%)

0

0

80/480c

1(1.4%)

1(1.4%)

1 (1.4%)

LUMARTEM

20/120

2 (2.7%)

0

0

80/480

1 (1.4%)

0

0

CO-METHER

20/120

5 (6.8%)

1 (1.4%)

0

KOMEFAN-140

20/120

1 (1.4%)

1(1.4%)

0

COMBIART

20/120

5 (6.8%)

0

0

LUMERAX

20/120

1 (1.4%)

1 (1.4%)

0

LARIACT

20/120

3 (4.1%)

0

1 (1.4%)

Cach-ARTb

20/120

2 (2.7%)

2 (2.7%)

1 (1.4%)

LUMAREN

20/120

2 (2.7%)

0

0

COARTEM

20/120

1 (1.4%)

0

0

KOMEFAN

20/120

1 (1.4%)

0

0

LUMITER

20/120

6 (8.1%)

1 (1.4%)

0

Not Indicated

20/120

4 (5.4%)

0

0

Total number

74 (100%)

11 (14.9%)

5(6.8%)

  1. aWHO and US Pharmacopeia (90–110%)
  2. bOne batch (CHRT21001E) of this brand failed both artemether and lumefantrine assay test
  3. cThe sample was not registered for use in the country by the National drug regulator and was classified as substandard regardless of assay results as per the WHO guidelines