What it isAntimalarial impairing parasite heme detoxification; malaria treatment and prophylaxis.
Why this oneIts long action permits weekly prophylaxis and retains value where chloroquine resistance is widespread.
What limits itVivid dreams, anxiety, psychosis, and other neuropsychiatric effects can persist after stopping; avoid in psychiatric or seizure history.
BOXED WARNING May cause neuropsychiatric adverse reactions that can persist after discontinuation; do not use for prophylaxis in patients with major psychiatric disorders; discontinue and substitute if psychiatric or neurologic symptoms occur during prophylaxis.
FDA dosing
Population
Start
Target
Max
Malaria treatment (mild-moderate, P. falciparum or P. vivax)
Adult
1250 mg (5 tab) as a single oral dose
single dose
Malaria prophylaxis
Adult
250 mg once weekly
250 mg weekly
Malaria treatment (P. falciparum)
Peds ≥6 mo
20–25 mg/kg (may split into 2 doses 6–8 h apart); not to exceed adult dose
1250 mg
Malaria prophylaxis
Pediatric
~5 mg/kg once weekly (weight-based tablet fractions; 250 mg if >45 kg)
250 mg weekly
Renal Undefined
Hepatic Undefined
If no improvement within 48–72 h, do not retreat with mefloquine; after P. vivax, follow with an 8-aminoquinoline (e.g., primaquine) to prevent relapse.
Instructions
Do not take on an empty stomach; take with at least 8 oz (240 mL) water.
Prophylaxis: begin 1 week before travel, take same day each week (preferably after main meal), continue 4 weeks after leaving the endemic area.
Tablets may be crushed and suspended in liquid for children unable to swallow whole.
If vomiting occurs <30 min after a treatment dose, repeat full dose; if 30–60 min, give an additional half-dose.
Contraindications
Hypersensitivity to mefloquine or related compounds (quinine, quinidine).
Prophylaxis in patients with active/recent depression, generalized anxiety disorder, psychosis, schizophrenia, other major psychiatric disorders, or a history of convulsions.
Cautions
Neuropsychiatric reactions (anxiety, depression, hallucinations, psychosis) that may persist after stopping.
Dizziness, vertigo, tinnitus, loss of balance — may be prolonged or permanent.
Defining liabilityGenerally tolerated at therapeutic doses; clinically important risks are agent-specific and increase with interactions or organ impairment.