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Dihydroartemisinin–piperaquine

  • AntimalarialsAntimalarials

Oral artemisinin combination for uncomplicated malaria: a fast, short-lived artemisinin plus piperaquine, which stays in the body for weeks.

Updated

Also called: artenimol and piperaquine, DHA-PPQ

Quick facts

Group
Antimalarials
Target
Parasite heme (dihydroartemisinin is activated by heme iron; piperaquine blocks heme detoxification)
Used for
Uncomplicated malaria · Malaria by Plasmodium vivax
Key effects
Headache · Nausea · Small
Monitor
Fever and a blood film · Vomiting soon after a dose
ATC
P01BF05

No doses: the clinician sets them by the current guideline.

Mechanism of action

Dihydroartemisinin is the active form of the artemisinins: heme iron inside the parasite opens its endoperoxide bridge and the free radicals damage many parasite proteins, so the parasite load falls within hours. Piperaquine, a bisquinoline related to chloroquine, is thought to stop the parasite from turning toxic heme into hemozoin. Because it is eliminated very slowly, it kills the parasites that survive the short artemisinin course and protects for some weeks after treatment.

  1. Heme iron opens dihydroartemisinin's endoperoxide bridge
  2. Free radicals damage parasite proteins and clear parasites fast
  3. Piperaquine blocks heme detoxification in the food vacuole
  4. Slowly cleared piperaquine kills the remaining parasites

Indications

  • Uncomplicated malaria by Plasmodium falciparum (WHO-recommended artemisinin-based combination) Malaria →
  • Malaria by Plasmodium vivax (blood stage; primaquine or tafenoquine is still needed against liver hypnozoites) Malaria →
  • Studied and considered by WHO for preventive therapy and mass drug administration

Adverse effects

Common

  • Headache, dizziness and weakness
  • Nausea, vomiting and abdominal pain
  • Small, transient prolongation of the QT interval

Contraindications

  • Allergy to either component
  • Severe malaria (it is an oral treatment; severe malaria needs injectable artesunate)

Key interactions

Other QT-prolonging medicines (some antiarrhythmics, macrolides, fluoroquinolones, antipsychotics, other quinoline antimalarials)
Additive QT prolongation; caution, above all with heart disease or a family history of sudden death.
Fatty food
Raises piperaquine levels several-fold and with them the effect on the QT interval; taken on an empty stomach.
A new antimalarial course soon after
Piperaquine is still present for weeks; the overlap is taken into account when another antimalarial is started.

What is monitored

  • Fever and a blood film or rapid test to confirm the parasites have gone
  • ECG in people with heart disease, electrolyte disorders or other QT-prolonging drugs
  • Vomiting soon after a dose (the dose may need repeating under medical guidance)

Administration and safety

  • Oral three-day course, with water and away from meals
  • Dispersible forms exist for small children
  • Not for severe malaria: injectable artesunate is used instead

Pregnancy and breastfeeding

Choice of antimalarial in pregnancy follows WHO and national guidance, which differ by trimester; a clinician decides.

Nursing care

  • Confirm malaria by microscopy or rapid test before treatment
  • Give the doses away from food and check whether the patient vomits them
  • Ask about heart disease, fainting and other QT-prolonging medicines
  • Teach to return if fever persists or danger signs appear

Pharmacokinetics

Absorption
Oral. A high-fat meal raises piperaquine absorption about threefold, so the tablets are taken fasting.
Half-life
Dihydroartemisinin about 1 to 2 hours; piperaquine about 22 days in healthy volunteers.

Test yourself

Think of the answer, then tap the question to see it.

Why is dihydroartemisinin combined with piperaquine instead of being given alone?

The artemisinin acts fast but is cleared within hours; the slowly eliminated partner kills the survivors and protects against resistance.

Why are dihydroartemisinin–piperaquine tablets taken fasting?

A fatty meal raises piperaquine absorption several-fold, and higher levels prolong the QT interval more.

Which ECG effect is linked to piperaquine?

Prolongation of the QT interval, so other QT-prolonging drugs are used with caution.

Can dihydroartemisinin–piperaquine treat severe malaria?

No. It is an oral treatment for uncomplicated malaria; severe malaria needs injectable artesunate.

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Educational content on how drugs work; not a prescribing guide and no substitute for a health professional's advice. No doses are given.

Sources: Notes on the Design of Bioequivalence Study: Dihydroartemisinin / Piperaquine Tetraphosphate (World Health Organization (WHO Prequalification), 2026); Meeting report of the Evidence Review Group on the cardiotoxicity of antimalarials (World Health Organization (WHO), 2017); eEML - Electronic Essential Medicines List (World Health Organization (WHO), 2026); Malaria (World Health Organization (WHO), 2026).

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