Skip to main content
. 2023 May 26;22:165. doi: 10.1186/s12936-023-04600-8

Table 2.

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

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%)

aWHO and US Pharmacopeia (90–110%)

bOne batch (CHRT21001E) of this brand failed both artemether and lumefantrine assay test

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