Plasmodium falciparum malaria

Active Ingredient: Mefloquine

Indication for Mefloquine

Population group: only children (1 year - 12 years old) , adolescents (12 years - 18 years old) , adults (18 years old or older)

Mefloquine is especially indicated for therapy of plasmodium falciparum malaria in which the pathogen has become resistant to other antimalarial agents.

Following treatment of P. vivax malaria with mefloquine, relapse prophylaxis with an 8-amino-quinoline derivative, for example primaquine, should be considered in order to eliminate parasites in the hepatic phase.

For this indication, competent medicine agencies globally authorize below treatments:

20–25 mg/kg in 2-3 divided doses daily

Route of admnistration

Oral

Defined daily dose

20 - 25 mg per kg of body weight

Dosage regimen

From 6.667 To 8.333 mg per kg of body weight 3 time(s) per day every day for 3 day(s)

Detailed description

The recommended total therapeutic dose of mefloquine is 20–25 mg/kg.

The recommended total therapeutic dosages of mefloquine tablets relative to body weight are presented in the following table:

Body WeightTotal dose
<20 kg*¼ tablet/2.5–3 kg
1 tablet/10–12 kg
20–30 kg2–3 tablets
>30–45 kg3–4 tablets
>45–60 kg4–5 tablets
>60 kg**6 tablets

* Experience with mefloquine in infants less than 3 months old or weighing less than 5 kg is limited.
** There is no specific experience with total dosages of more than 6 tablets in very heavy patients.

In order to limit the occurrence and severity of adverse reactions, the total therapeutic dose may be split into 2–3 doses (e.g. 3 + 1, 3 + 2 or 3 + 2 + 1 tablets) taken 6–8 hours apart.

A second full dose should be given to patients who vomit less than 30 minutes after receiving the drug. If vomiting occurs 30–60 minutes after a dose, an additional half-dose should be given.

If a full treatment course with mefloquine does not lead to improvement within 48–72 hours, alternative treatments should be considered.

Mefloquine can be given for severe acute malaria after an initial course of intravenous quinine lasting at least 2–3 days. Interactions leading to adverse events can largely be prevented by allowing an interval of at least 12 hours after the last dose of quinine.

Artemisinin combination therapy (ACT) is recommended as the standard of care for treatment of P. falciparum malaria, regardless of region of acquisition. Mefloquine is a recommended partner molecule for inclusion in ACT.

Active ingredient

Mefloquine

Mefloquine acts on and destroys the asexual intraerythocytic forms of the human malaria parasites: Plasmodium falciparum, P. vivax. P. malariae and P. ovale. It is effective in the treatment and prophylaxis of malaria.

Read more about Mefloquine

Related medicines

Develop a tailored medication plan for your case, considering factors such as age, gender, and health history

Ask the Reasoner

Liability Disclaimer : RxReasoner has utilized reasonable care in providing content and services that are accurate, complete and up to date. However, RxReasoner does not accept any responsibility or liability about it. The content and services of RxReasoner are for informational purposes only and they are not intended to be a substitute for the knowledge, expertise, skill, and judgment of physicians, pharmacists, nurses, or other healthcare professionals involved in patient care. RxReasoner offers no medical advice. Users are responsible for the use of the provided content. A shown indication or treatment should not be construed to indicate that the medication is safe, appropriate, or effective in any given patient or under any particular circumstances. The absence of an indication or treatment should not roule out the existence of other appropriate medications. Always seek the advice of a physician or other qualified health provider with any questions you may have regarding a medical condition or medicament. RxReasoner is not liable for any damages allegedly sustained arising out of the use of its content and services.