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New search Medicine profile Artesunate sodium

Clinical medicine profile

Artesunate sodium

Antimalarial

POM
Evidence state Source not available Reviewed 14 Aug 2026
Route
ORAL / PARENTERAL (severe malaria)
Schedule
POM
ATC
Not assigned
PPB status
registered
Patient advice Check interactions
Verification required

This profile needs source confirmation

A traceable source link is not attached to this profile. Confirm prescribing decisions against the current SmPC and Kenya STG/EML.

01 Risk first

Safety essentials

The information most likely to change a prescribing or dispensing decision.

Contraindications

  • Known hypersensitivity.
  • Agent-specific: e.g. mefloquine in active depression/psychosis/seizure disorder
  • primaquine in G6PD deficiency (haemolysis).
  • Always check agent-specific absolute contraindications.

Precautions

  • Confirm species and severity.
  • ECG risk with some agents (quinine, piperaquine).
  • Pregnancy: follow Kenya/WHO trimester-specific ACT guidance.
  • Vomiting within 30–60 min may need redosing per protocol.
02 Point of care

Dosing matrix

Population and organ-function guidance, shown together for faster comparison.

Adult

2.4 mg/kg body weight IV or IM given on admission [time = 0], then at 12 h and 24 h, then once a day. Artesunate reconstituition: Step 1: The powder for injection should be reconstituted with 1mL of 5% sodium bicarbonate and shaken vigorously till the solution becomes clear. Step 2: For I.V. use, add 5 mL [2mL for I.M. use] of normal saline or 5% of glucose and mix again. Step 3: For I.V. use, the required amount of the drug is administered slowly over a period of 2 - 3 minutes. The powder for injection is difficult to dissolve and care should be taken to ensure that it is completely dissolved before parenteral administration. It should always be used immediately after reconstitution. If the solution is cloudy or a precipitate is present, the parenteral preparation should be discarded.

Paediatric

See label paediatric section if present; otherwise use paediatric formulary — do not extrapolate adult doses.

Renal

Supportive care critical in severe malaria; adjust supportive drugs as needed.

  • CrCl 0–120: Confirm renal dosing in product SmPC / primary label.
Hepatic

Monitor if pre-existing liver disease; many agents hepatically metabolised.

03 Clinical use

Use, effects & interactions

Indications

  • Therapeutic use is agent- and indication-specific within the class (Antimalarial).
  • Use according to culture results, national guidelines (Kenya STG/EML where applicable) and the current product SmPC.
  • See under artemether.

Adverse effects

  • GI upset, headache, dizziness, sleep disturbance (mefloquine).
  • Serious: cardiotoxicity, neuropsychiatric effects, haemolysis (primaquine in G6PD def.), cinchonism (quinine).
  • Kenya: follow current MoH malaria guidelines for uncomplicated vs severe disease.
  • Test before treat when feasible.
  • Complete full ACT course.
  • Severe malaria is an emergency — parenteral artesunate, not oral therapy alone.
04 Pharmacology

Mechanism & disposition

Artemisinins generate carbon-centred free radicals after activation by parasite haem-iron, damaging parasite proteins and membranes — rapid blood schizonticidal effect.

Artemisinins generate carbon-centred free…Partner drugs (lumefantrine, piperaquine,…Other classes act on haem detoxification,…
Read complete mechanism

Artemisinins generate carbon-centred free radicals after activation by parasite haem-iron, damaging parasite proteins and membranes — rapid blood schizonticidal effect. Partner drugs (lumefantrine, piperaquine, etc.) provide longer-acting clearance of residual parasites. Other classes act on haem detoxification, electron transport, or folate pathways depending on agent.

Onset

Hours (artemisinins rapid parasite clearance)

Duration

Regimen-dependent (ACT 3 days typical)

Route

ORAL / PARENTERAL (severe malaria)

Absorption

enhanced by fat-containing food. Complex

Metabolism

(CYP3A4) for several partners. Severe malaria: parenteral artesunate preferred first-line in most guidelines.

05 Special populations

Pregnancy, lactation & diet

Pregnancy

Treat malaria — untreated infection risks mother and fetus. Use trimester-appropriate regimens per Kenya MoH / WHO.

Lactation

Most first-line ACTs compatible; continue breastfeeding with maternal treatment.

06 Kenya market

Brands & loaded prices

From
Median
Listings1
BrandManufacturerPackObserved price
Artecor Signature tabs 1's Unavailable
07 Provenance

Sources & review state

Primary sourceLocal active-ingredient clinical extract; Professional class pharmacology (Antimalarial)
Last reviewed14 Aug 2026
EvidenceSource not available

Decision support only. Confirm patient-specific decisions against the current product SmPC, Kenya STG/EML, and professional judgement.