Registered Malawi · PMRA

ARTESIANE 20MG/ML INJECTION

BETA-ARTMETHER

PMPB/PL263/4 INJECTION

What it does

Beta-artmether is a medication used to treat malaria, a serious infection caused by parasites transmitted through mosquito bites.

Commonly used for: malaria (malaria infection)

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Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.

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Registration & product details

Registration no.
PMPB/PL263/4
Registration date
23/04/2003
Expiry date
30/06/2014
Status
Registered
Active ingredient
BETA-ARTMETHER
Dosage form
INJECTION
Strength
-
Pack size
-
Therapeutic class
-
Manufacturer / MAH
-
Applicant / LTR
-
Country of origin
-

Source: Pharmacy and Medicines Regulatory Authority · fetched 2026-04-21 17:37:39 · updated 2026-09-29 04:33:04

Disclaimer: This information is sourced from Pharmacy and Medicines Regulatory Authority (Malawi). Always consult a qualified healthcare professional before using any medication.

About this medicine

Beta-artmether is a medication used to treat malaria, a serious infection caused by parasites transmitted through mosquito bites.

What it treats

  • malaria (malaria infection)

How it works

It works by killing the malaria parasites in the blood.

Who it's for

This medicine is for people diagnosed with malaria.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: betaartmether

Betaartmether is an antimalarial drug that belongs to the artemisinin class. It is derived from the sweet wormwood plant (Artemisia annua). The drug is primarily used for the treatment of uncomplicated Plasmodium falciparum malaria, particularly in areas where resistance to other antimalarial medications has been reported. It is administered orally and is often combined with other antimalarial agents to enhance efficacy and reduce the risk of resistance.

Indications

  • Uncomplicated Plasmodium falciparum malaria
  • Malaria prophylaxis in endemic areas (when used in combination therapy)

Dosage

Children: Refer to local guidelines and BNF for Children for specific dosing information, as paediatric dosing is typically weight-based and may vary depending on age and clinical condition.

Adults: Refer to local guidelines and BNF for specific dosing information, as individual patient factors and regional resistance patterns can influence dosing.

Mechanism of action

Betaartmether exerts its antimalarial effects through the generation of reactive oxygen species (ROS) after activation by heme, which is released during the digestion of hemoglobin by malaria parasites. These ROS cause damage to the parasite's membranes and proteins, leading to its death. The drug is thought to also interfere with the parasite's ability to regulate calcium homeostasis, further contributing to its efficacy.

Pharmacodynamics

Betaartmether is rapidly effective against early-stage malaria infections. It acts quickly to reduce parasitemia and alleviate symptoms associated with malaria. The drug's quick action is beneficial in treating acute malaria episodes, although it does not provide long-term prophylaxis. Its antimalarial activity is dose-dependent, with higher doses correlating with more significant reductions in parasite load.

Pharmacokinetics

Betaartmether is absorbed efficiently in the gastrointestinal tract, with peak plasma concentrations typically reached within 1 to 2 hours post-administration. It has a relatively short half-life, which necessitates multiple doses or combination therapy to maintain therapeutic levels. The drug is extensively metabolized in the liver, primarily by cytochrome P450 enzymes, leading to active metabolites that also contribute to its antimalarial effect. Excretion occurs mainly via the kidneys, emphasizing the need for caution in patients with renal impairment.

Adverse effects

  • Nausea
  • Vomiting
  • Diarrhea
  • Abdominal pain
  • Headache
  • Dizziness
  • Fatigue

Precautions

  • Monitor liver function during treatment.
  • Use with caution in patients with a history of hypersensitivity to artemisinin derivatives.
  • Caution in patients with pre-existing conditions such as epilepsy or other seizure disorders.

Pregnancy

Betaartmether should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. Consult a healthcare professional.

Breast-feeding

Betaartmether is excreted in breast milk. Caution is advised when administering to nursing mothers.

Storage

Store in a cool, dry place, away from direct sunlight. Keep out of reach of children.

Formulations

  • Oral tablets
  • Injectable solution

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.