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ARTICLE AD BOX
The National Agency for Food and Drug Administration Control, NAFDAC, has reminded Nigerians that multi-dose Artemether/Lumefantrine adust pulverization for oral suspension is nary longer approved for registration oregon usage successful the country.
The bureau made this known successful a connection connected Friday, 27th February, 2026, reminding the nationalist of an earlier regulatory directive released successful 2025.
According to NAFDAC, the determination affects each locally manufactured and imported brands of the multi-dose anti-malaria suspension.
NAFDAC explained that the medicine was discontinued due to the fact that the cause becomes unstable aft it is mixed with water, causing it to suffer its effectiveness.
“This regulatory directive was taken owed to the instability of the reconstituted formulations, which results successful nonaccomplishment of efficacy of the suspension,” the bureau said.
The bureau noted that studies person shown that erstwhile the cause loses its strength, it whitethorn nary longer dainty malaria properly. This, it warned, could pb to worsening illness, attraction failure, superior complications, and, successful terrible cases, death.
NAFDAC further stated that it nary longer accepts new, renewal, oregon saltation applications for multi-...
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