Lumefantrine (Coartem/Riamet)
Pronunciation: loo-me-FAN-treen.
- Generic name
- lumefantrine (only marketed combined with artemether)
- Drug class
- Antimalarial (aryl amino alcohol) combined with artemether (an artemisinin derivative) as a fixed-dose artemisinin-combination therapy (ACT)
- Form
- Tablet (20 mg artemether / 120 mg lumefantrine), or dispersible tablet in some markets
- Route
- Oral
- Legal status
- Prescription-only
Availability and supply rules vary by country
Trade names by country: United States · United Kingdom · Australia · New Zealand
Australia: Coartem (artemether/lumefantrine) (5) · Full directory
What lumefantrine (only marketed combined with artemether) is and how it works
Lumefantrine is an antimalarial medicine that is only ever combined with a second antimalarial, artemether, in a single tablet. This combination (Coartem or Riamet) is used to treat acute, uncomplicated malaria caused by Plasmodium falciparum, the most dangerous type of malaria parasite. Artemether acts quickly to reduce the parasite level, while lumefantrine stays in the body longer to help clear the infection completely and reduce the risk of the parasite becoming resistant. (1)
This medicine must be taken with food -- taking it on an empty stomach can mean the medicine is not absorbed properly, and the malaria may not be fully treated. It can also affect the heart's electrical rhythm (QT interval), so tell your care team about any heart rhythm problems or other medicines you take before starting.
Mechanism of action: how lumefantrine (only marketed combined with artemether) works
Artemether is rapidly converted to the active metabolite dihydroartemisinin and acts quickly against blood-stage parasites; lumefantrine has a much longer elimination half-life and clears residual parasites, reducing recrudescence and resistance risk. Both components require adequate lipid intake for optimal oral bioavailability. (1)
What lumefantrine (only marketed combined with artemether) is used for
Acute, uncomplicated Plasmodium falciparum malaria
Used to treat acute, uncomplicated malaria caused by Plasmodium falciparum in adults and children 2 months of age and older weighing 5 kg or more. It is not approved for severe or complicated malaria, and it is not used to prevent malaria (it is not a prophylactic/preventive medicine). (1) (3)
Before taking lumefantrine (only marketed combined with artemether)
Do not take / not appropriate for
- Do not take if you have a known allergy to artemether, lumefantrine, or any ingredient in the tablet. (all countries) (1)
- Do not take together with strong CYP3A4-inducing medicines, including rifampin, carbamazepine, phenytoin, or St. John's wort -- these can make the treatment less effective. (all countries) (1)
- Do not take halofantrine within one month of this medicine, because the combined effect on heart rhythm (QT interval) can be dangerous. (all countries) (1)
- Avoid if you have congenital long QT syndrome, a family history of sudden cardiac death, uncorrected low potassium or magnesium levels, or if you take other medicines that affect heart rhythm, unless your clinician judges the malaria treatment benefit outweighs this risk. (all countries) (1)
Tell your clinician about
- Any personal or family history of heart rhythm problems, including long QT syndrome or sudden cardiac death.
- All other medicines you take, especially anything that affects heart rhythm, HIV antiretroviral medicines, and any recent use of quinine or halofantrine.
- Whether you are able to eat food around the time of each dose -- this medicine must be taken with food to work properly.
- Whether you are pregnant, planning pregnancy, or breastfeeding.
How to take lumefantrine (only marketed combined with artemether)
- Always take each dose with food -- fat in food greatly increases how much of this medicine your body absorbs (up to about 16-fold for lumefantrine), and taking it without food can mean the malaria is not fully treated.
- Follow the exact dosing schedule given to you: an initial dose, then further doses at set time points over about 3 days (60 hours) -- do not skip or reschedule doses without your care team's guidance, since completing the exact course matters for curing the infection and preventing resistance.
- If you are prescribed quinine after finishing this medicine, tell that prescriber, since lumefantrine stays in the body for a long time and close heart-rhythm (ECG) monitoring may be advised.
Procedures and treatment changes
Tell the treating team before surgery, procedures, or any medicine change. Do not alter treatment without the responsible clinician. (1) (2) (3) (4) (5) (6)
Missed dose
Contact your prescriber or care team as soon as possible if a dose is missed or delayed -- completing this specific 6-dose schedule correctly and on time matters for curing the malaria infection and reducing resistance risk, so do not simply skip or take an extra dose on your own.
Overdose
Seek urgent medical attention if too much of this medicine has been taken, or if you notice an irregular or fast heartbeat, severe dizziness, or fainting, since this medicine can affect heart rhythm. (1)
Side effects
Side effects and their urgency vary; report severe, persistent, or concerning symptoms.
Headache, dizziness, and tiredness (asthenia).
What to notice: Headache, dizziness, and tiredness (asthenia).
What to do: Discuss persistent or troublesome symptoms with the treating clinician or pharmacist. (1)
Loss of appetite (anorexia).
What to notice: Loss of appetite (anorexia).
What to do: Discuss persistent or troublesome symptoms with the treating clinician or pharmacist. (1)
Joint and muscle pain (arthralgia, myalgia) in adults.
What to notice: Joint and muscle pain (arthralgia, myalgia) in adults.
What to do: Discuss persistent or troublesome symptoms with the treating clinician or pharmacist. (1)
Fever, cough, and vomiting, more commonly reported in children.
What to notice: Fever, cough, and vomiting, more commonly reported in children.
What to do: Discuss persistent or troublesome symptoms with the treating clinician or pharmacist. (1)
Serious warnings
Signs of an irregular heartbeat (QT prolongation) — high caution
Symptoms: Palpitations, a fast or irregular heartbeat, severe dizziness, or fainting.
Action: Seek urgent medical attention -- this medicine can affect the heart's electrical rhythm, and this risk is higher with certain other medicines, low potassium or magnesium, or an existing heart-rhythm condition. (1)
Treatment failure from taking the medicine without food — moderate
Symptoms: Ongoing or returning fever, chills, and other malaria symptoms after completing the course.
Action: Contact your care team promptly if malaria symptoms continue or return -- this medicine needs to be taken with food to be absorbed properly, and inadequate food intake during treatment is linked to a higher chance the infection is not fully cleared. (1)
Signs of a serious allergic reaction — emergency
Symptoms: Swelling of the face, lips, tongue, or throat; difficulty breathing; widespread rash or hives.
Action: Seek emergency medical help immediately. (1)
Signs of delayed anaemia (haemolytic anaemia) — moderate
Symptoms: Unusual tiredness, pale skin, yellowing of the skin or eyes, or dark urine appearing days to weeks after treatment.
Action: Contact your care team promptly for blood tests -- this is a recognised, though uncommon, delayed reaction that has been reported after treatment. (1)
Interactions
- Strong CYP3A4-inducing medicines (rifampin, carbamazepine, phenytoin, St. John's wort) can make this medicine less effective and must not be combined with it. (1)
- CYP3A4-inhibiting medicines can raise levels of this medicine and increase the risk of heart-rhythm effects -- combine only with caution and medical guidance. (1)
- This medicine inhibits CYP2D6, which can raise the levels and effects (including cardiac effects) of other medicines broken down by that enzyme. (1)
- Halofantrine must not be taken within one month of this medicine because of additive heart-rhythm (QT-prolongation) risk. (1)
- If quinine is given after this medicine, close heart-rhythm (ECG) monitoring is advised because of lumefantrine's long elimination half-life. (3)
- Caution is advised with antiretroviral (HIV) medicines -- discuss with your care team if you are on HIV treatment. (1)
Pregnancy, breastfeeding, kidney/liver function, age
Pregnancy
This medicine does not have a formal FDA pregnancy risk category. Available human data have not shown a clear increase in major birth defects or adverse pregnancy outcomes, though animal studies at higher doses showed fetal loss. Because untreated malaria itself poses a serious risk to both mother and baby, treatment is generally still recommended in pregnancy when needed -- this decision should be made with your care team. (1) (2) (3) (4) (5) (6)
Breastfeeding
Discuss breastfeeding with your care team if you are prescribed this medicine -- specific breastfeeding safety data was not detailed with high confidence in the sources reviewed for this dossier. (1) (2) (3) (4) (5) (6)
Children
Approved for children 2 months of age and older weighing 5 kg or more, with weight-banded dosing. (1) (2) (3) (4) (5) (6)
Elderly
No specific age-based dose adjustment is described in the sources reviewed, though the same heart-rhythm and interaction cautions apply. (1) (2) (3) (4) (5) (6)
Hepatic_impairment
Not specifically detailed in the sources reviewed for this dossier -- discuss with your care team if you have significant liver disease. (1) (2) (3) (4) (5) (6)
Renal_impairment
Not specifically detailed in the sources reviewed for this dossier -- discuss with your care team if you have significant kidney disease. (1) (2) (3) (4) (5) (6)
Source_ids
Monitoring
Before starting
- Personal/family history of heart-rhythm problems
- Current medicines, especially CYP3A4/CYP2D6-interacting and QT-affecting medicines
- Ability to take the medicine with food
- Pregnancy/breastfeeding status
During treatment
- Watch for palpitations, irregular heartbeat, severe dizziness, or fainting.
- Confirm each dose is taken with food.
- Watch for malaria symptoms continuing or returning after the course finishes, which may indicate treatment failure.
Storage
Store tablets as directed on the product packaging, typically at room temperature, away from moisture and out of reach of children.
Professional information
Clinician-facing context only, sourced from the current US DailyMed prescribing information and UK emc SmPC; verify against the current full label before prescribing.
United States, United Kingdom, European Union, Australia
Indication: Acute, uncomplicated P. falciparum malaria
Dose summary: 6 doses over ~60 hours (initial, then 8h, then twice daily for 2 more days), weight-banded 1-4 tablets per dose (5 to <15 kg, 15 to <25 kg, 25 to <35 kg, >=35 kg); must be taken with food.
Renal context: Not specifically detailed in the sources reviewed for this dossier. (1) (3)
Hepatic guidance
Not specifically detailed in the sources reviewed for this dossier.
Overdose note
Manage supportively, with particular attention to cardiac (QT-interval) monitoring given the heart-rhythm risk profile of this combination. (1)
Frequently asked questions
Can I get lumefantrine on its own, without artemether?
No. Lumefantrine has never been marketed or used as a standalone medicine -- it is only available combined with artemether in a single tablet (Coartem in the US, Australia, and most countries; Riamet in the UK). (2) (1)
Why do I need to take this medicine with food?
Food, especially fat, greatly increases how well this medicine is absorbed -- up to about 16-fold for lumefantrine. Taking it without food can mean not enough medicine gets into your body to fully clear the malaria infection. (1)
Is this medicine available everywhere?
Its availability genuinely differs by country: it is currently authorised in the United States, United Kingdom, Australia, and (through national authorisations) the European Union. It was previously approved in New Zealand but is no longer currently available there. A standard Health Canada market authorisation could not be confirmed for Canada in the sources reviewed. (1) (6) (7)
What is the mechanism of action of lumefantrine (only marketed combined with artemether)?
Artemether is rapidly converted to the active metabolite dihydroartemisinin and acts quickly against blood-stage parasites; lumefantrine has a much longer elimination half-life and clears residual parasites, reducing recrudescence and resistance risk. Both components require adequate lipid intake for optimal oral bioavailability. (1)
References
- COARTEM (artemether and lumefantrine) tablets -- full prescribing informationU.S. Food and Drug Administration / DailyMed (NIH), full prescribing information, Novartis · United States · accessed 2026-07-30 · source 1
- Confirmation that lumefantrine is never marketed as a standalone monotherapyPeer-reviewed pharmacology/clinical literature (multiple independent sources) · Global · accessed 2026-07-30 · source 2
- Riamet 20 mg/120 mg Tablets -- Summary of Product Characteristicselectronic medicines compendium (emc), United Kingdom, Novartis · United Kingdom · accessed 2026-07-30 · source 3
- Artemether/lumefantrine -- list of nationally authorised medicinal products, PSUSA/00000236European Medicines Agency (EMA), list of nationally authorised medicinal products · European Union · accessed 2026-07-30 · source 4
- COARTEM artemether/lumefantrine 20 mg/120 mg tablet -- ARTG entries 298287 / 158527Therapeutic Goods Administration (TGA), Australia · Australia · accessed 2026-07-30 · source 5
- Riamet (artemether/lumefantrine) -- historical New Zealand approval, product no longer availableMedsafe (New Zealand regulator) -- secondary confirmation of historical approval and current unavailability · New Zealand · accessed 2026-07-30 · source 6
- No confirmed Health Canada Drug Product Database entry located for Coartem/RiametN/A -- absence-of-evidence note, not a positive source · Canada · accessed 2026-07-30 · source 7
Brand names by country
Single-ingredient lumefantrine (only marketed combined with artemether) names are shown separately by country. Product availability, strengths, and supply rules can change; combination products are not included here.
Priority countries
United States
- Coartem (artemether/lumefantrine) (1)FDA approved currently labeled · 20 mg/120 mg · Novartis
United Kingdom
- Riamet (artemether/lumefantrine) (3)MHRA licensed emc smpc confirmed · 20 mg/120 mg · Novartis
Australia
- Coartem (artemether/lumefantrine) (5)TGA ARTG registered confirmed · 20 mg/120 mg tablet and dispersible tablet · Novartis Pharmaceuticals Australia Pty Ltd
New Zealand
- Riamet (artemether/lumefantrine) (6)previously Medsafe approved no longer currently available · 20 mg/120 mg tablet (2006); dispersible tablet (2011) · historical, per Medsafe records
View brands in additional countries.
European Union
Riamet / national equivalents (artemether/lumefantrine) (4)