LEVEL 4 P01BC02

Δραστικές

Φάρμακα

  • DRUGBANK - Mefloquine
  • indication:

    For the treatment of mild to moderate acute malaria caused by Mefloquineuine-susceptible strains of <i>Plasmodium falciparum</i> (both chloroquine-susceptible and resistant strains) or by <i>Plasmodium vivax</i>. Also for the prophylaxis of <i>Plasmodium falciparum</i> and <i>Plasmodium vivax</i> malaria infections, including prophylaxis of chloroquine-resistant strains of <i>Plasmodium falciparum</i>.

  • pharmacology:

  • mechanism:

    Mefloquine has been found to produce swelling of the <i>Plasmodium falciparum</i> food vacuoles. It may act by forming toxic complexes with free heme that damage membranes and interact with other plasmodial components.

  • toxicity:

    Oral, rat: LD<sub>50</sub> = 880 mg/kg. Symptoms of overdose include nausea, vomiting, and weight loss.

  • absorprion:

    Well absorbed from the gastrointestinal tract. The presence of food significantly enhances the rate and extent of absorption.

  • halflife:

    2 to 4 weeks

  • roouteelimination:

    There is evidence that mefloquine is excreted mainly in the bile and feces. Urinary excretion of unchanged mefloquine and its main metabolite under steady-state condition accounted for about 9% and 4% of the dose, respectively.

  • volumedistribution:

    * 20 L/kg [healthy adults]

  • clearance:

    * 30 mL/min