Injection Falcigo dosage

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Falcigo injection artesunate dosage dosing regimen severe malaria

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Here is the complete dosing information for Injection Falcigo (Artesunate for Injection):

Injection Falcigo (Artesunate) - Dosage

Brand: Falcigo Generic: Artesunate Available strengths: Powder for Injection - 60 mg and 120 mg vials

Indication

Treatment of severe malaria (including severe Plasmodium falciparum malaria) - first-line parenteral therapy per WHO and national guidelines.

Dosing Regimen

Adults and Children weighing ≥ 20 kg

TimeDoseRoute
0 h (admission)2.4 mg/kgIV or IM
12 h2.4 mg/kgIV or IM
24 h2.4 mg/kgIV or IM
Every 24 h thereafter2.4 mg/kgIV or IM
Continue until the patient can tolerate oral antimalarial therapy (usually 3 days minimum, then switch to oral).

Children weighing < 20 kg

  • 3 mg/kg/dose (higher dose to ensure equivalent drug exposure due to pharmacokinetic differences in small children)
  • Same schedule: 0 h, 12 h, 24 h, then once daily

Route of Administration

  • Intravenous (IV): Preferred route in severe malaria
  • Intramuscular (IM): Used when IV access is not available

Reconstitution (60 mg vial)

  1. Add 1 mL of 5% sodium bicarbonate to the vial - mix until dissolved (artesunate base)
  2. Then add 5 mL of 5% dextrose (D5W) or normal saline to make a 10 mg/mL solution
  3. Administer IV over 1-2 minutes (slow IV push) or as a short infusion

Follow-up Oral Therapy (Mandatory)

After parenteral artesunate, a complete course of oral antimalarial must be given:
  • ACT (Artemisinin-based Combination Therapy): e.g., Artemether-Lumefantrine (Coartem) x 3 days
  • For P. vivax or P. ovale: add an 8-aminoquinoline (e.g., Primaquine) to cover hypnozoite liver stages

Special Populations

PopulationAdjustment
Renal impairmentNo dose adjustment required
Hepatic impairmentNo dose adjustment required
PregnancyCan be used (benefit outweighs risk in severe malaria)

Key Points

  • Artesunate is the first-line treatment for severe malaria, replacing IV quinine (shown to reduce mortality vs. quinine in AQUAMAT and SEAQUAMAT trials)
  • Always follow with oral ACT after parenteral course
  • Monitor for post-artesunate delayed haemolysis (PADH) - rare but can occur 1-4 weeks after treatment, especially in high-parasitaemia patients
  • Check blood smear 4 hours after the 3rd dose to assess parasite clearance

Sources: WHO Guidelines for treatment of malaria; Medscape artesunate dosing; severemalaria.org; Park's Textbook of Preventive and Social Medicine
Clinical note: This information is for healthcare professionals. Always verify current national malaria treatment guidelines for your region, as recommendations may vary.
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