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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/22326
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dc.contributor.authorD. Bunnagen_US
dc.contributor.authorJ. Karbwangen_US
dc.contributor.authorC. Viravanen_US
dc.contributor.authorS. Chitamasen_US
dc.contributor.authorT. Harinasutaen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-08-10T08:45:57Z-
dc.date.available2018-08-10T08:45:57Z-
dc.date.issued1992-12-01en_US
dc.identifier.citationSoutheast Asian Journal of Tropical Medicine and Public Health. Vol.23, No.3 (1992), 377-382en_US
dc.identifier.issn00383619en_US
dc.identifier.other2-s2.0-0027074876en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0027074876&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/22326-
dc.description.abstractA comparative trial of the combination of mefloquine or MSP with tetracycline was carried out in fifty-one adult Thai male patients with acute falciparum malaria. The patients were randomized to receive either the combination of tetracycline (250 mg qid for 7 days) with mefloquine 4 tablets (1,000 mg) or with MSP 4 tablets (one tablet contains 250 mg mefloquine, 500 mg sulfadoxine and 25 mg pyrimethamine). Fifty patients had a complete 28-day follow-up period. Both regimens produced similar efficacy with no difference in adverse effects. In the mefloquine plus tetracycline group, the cure rate was 72% (18/25). One patient had an RIII response, the others showed initial response to the treatment with FCT and PCT of 40.7 ± 27.4 and 76.2 ± 34.2 hours (mean ± SD) respectively. However, 6 patients developed recrudescence between days 17 and 29 (RI), 3 of these had vomiting. In the MSP plus tetracycline group, the cure rate was 76% (19/25). The means (± SD) of FCT and PCT were 44.7 ± 38.0 and 80.6 ± 25.0 hours, respectively. Six patients had recrudescence between days 17 and 31 (RI), 2 of these had vomiting. Although the addition of tetracycline improved the cure rate of mefloquine when compared with standard dose of mefloquine alone (3 tablets), these combinations seem to be useful in areas where alternative drugs are not available.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0027074876&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleClinical trials of mefloquine with tetracyclineen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
Appears in Collections:Scopus 1991-2000

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