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J Vector Borne Dis ; 2003 Sep-Dec; 40(3-4): 65-72
Article in English | IMSEAR | ID: sea-118033

ABSTRACT

Antimalarial drug resistance has now become a serious global challenge and is the principal reason for the decline in antimalarial drug efficacy. Malaria endemic countries need inexpensive and efficacious drugs. Preserving the life spans of antimalarial drugs is a key part of the strategy for rolling back malaria. Artemisinin-based combinations offer a new and potentially highly effective way to counter drug resistance. Clinical trials conducted in African children have attested to the good tolerability of oral artesunate when combined with standard antimalarial drugs. The cure rates of the different combinations were generally dependent on the degree of resistance to the companion drug. They were high for amodiaquine-artesunate, variable for sulfadoxine/pyrimethamine-artesunate, and poor for chloroquine-artesunate.


Subject(s)
Africa , Amodiaquine/therapeutic use , Animals , Antimalarials/therapeutic use , Artemisinins/therapeutic use , Chloroquine/therapeutic use , Drug Combinations , Drug Resistance , Drug Therapy, Combination , Humans , Latin America , Malaria, Falciparum/drug therapy , Plasmodium falciparum/growth & development , Pyrimethamine/therapeutic use , Randomized Controlled Trials as Topic , Sesquiterpenes/therapeutic use , Sulfadoxine/therapeutic use , World Health Organization
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