Please use this identifier to cite or link to this item: http://dspace.lamu.edu.zm:8080/handle/123456789/176
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dc.contributor.authorEKUE, KOFI, J. M.-
dc.contributor.authorSIMOOYA, O.O-
dc.contributor.authorSHETH, U. K.-
dc.contributor.authorWERNSDORFER, W. H.-
dc.contributor.authorNJELESANI, Evarist-
dc.date.accessioned2022-06-10T14:14:02Z-
dc.date.available2022-06-10T14:14:02Z-
dc.date.issued1985-
dc.identifier.issn00085-0146-
dc.identifier.urihttp://155.0.177.102:8080/jspui//xmlui/handle/123456789/176-
dc.descriptionThis article can be accessed at this link: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2536395/pdf/bullwho00085-0146.pdfen_US
dc.description.abstractFansimef is a combination of 250 mg of mefloquine, 500 mg of sulfadoxine, and 25 mg of pyrimethamine per tablet. A total of 150 adult male Zambian patients who had symptomatic Plasmodium falciparum parasitaemia were treated in a double-blind randomized fashion with either one, two or three tablets of Fansimef. All patients in the three treatment groups showed an S-type response. The rates of clearance of parasitaemia and fever were similar in all treatment groups. Tolerance was good at all dose levels. The main side-effects were abdominal discomfort, weakness and lassitude, dizziness, and pruritus, but these were mild, transient and required no specific treatment. Vomiting occurred only in 4% of patients given the highest dose of three tablets. The results of various haematological and biochemical investigations and urinalysis were not adversely altered by the administration of Fansimef.en_US
dc.description.sponsorshipNational Library of Medicineen_US
dc.language.isoenen_US
dc.publisherWorld Health Organizationen_US
dc.relation.ispartofseriesNational Center for Biotechnology Information;Vol. 63, Unit 2.-
dc.subjectmefloquineen_US
dc.subjectsulfadoxineen_US
dc.subjectpyrimethamineen_US
dc.subjectmalariaen_US
dc.titleA double-blind clinical trial of a combination of mefloquine, sulfadoxine and pyrimethamine in symptomatic falciparum malariaen_US
dc.typeArticleen_US
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