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Pharmacokinetics of mefloquine in treatment failure.

Abstract
The pharmacokinetics of mefloquine at the therapeutic dose of 750 mg single orally were compared between cured and recrudescent patients with acute uncomplicated falciparum malaria. Mefloquine was well-tolerated during the study. The side-effects found were nausea, vomiting and diarrhea. Five patients showed R-I and two showed R-II types of response. All recrudescent patients came from the eastern border of Thailand. The time taken to clear the parasites (PCT) was significantly longer in patients with recrudescence (99.6 +/- 36.9 and 63.0 +/- 8.9 hours); however, there was no difference regarding fever clearance time (FCT: 39.0 +/- 16.1 and 31.0 +/- 21.3 hours). The maximum concentration (Cmax) and the concentration on the first and second days in cured patients were significantly higher than those of treatment failure patients. Other pharmacokinetic parameters appeared to be similar in both groups. The present study indicates the existence of mefloquine-resistant falciparum malaria in the eastern border of Thailand. Inadequate mefloquine concentration may play an important role in this aspect. In addition, this study also suggests that Cmax or the concentrations on the first or second day of treatment may be used as guidelines to predict the outcome of treatment.
AuthorsJ Karbwang, K Na Bangchang, A Thanavibul, D Bunnag, T Harinasuta
JournalThe Southeast Asian journal of tropical medicine and public health (Southeast Asian J Trop Med Public Health) Vol. 22 Issue 4 Pg. 523-6 (Dec 1991) ISSN: 0125-1562 [Print] Thailand
PMID1820638 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Mefloquine
Topics
  • Absorption
  • Adolescent
  • Adult
  • Diarrhea (etiology)
  • Humans
  • Malaria, Falciparum (drug therapy)
  • Male
  • Mefloquine (metabolism, pharmacokinetics, therapeutic use)
  • Nausea (etiology)
  • Recurrence
  • Thailand
  • Vomiting (etiology)

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