Drug reference
amphotericin b (liposomal)
Drug monograph
CDSCO approved
EXCRETION
—
not curated
INTERACTIONS
—
none in our sources
PREGNANCY
—
not curated
Mechanism
Lipid formulations are preferentially taken up by reticuloendothelial tissues. This allows a large amount of drug to be delivered over a short period with less free drug available to cause toxicity.
Indications
Visceral Leishmaniasis (VL) (preferred in Bihar, India, and Mediterranean countries; preferred drug of choice globally)Visceral Leishmaniasis (VL) in HIV co-infection (drug of choice for primary treatment and relapses)Post-kala-azar dermal leishmaniasis (PKDL)Mucosal Leishmaniasis (ML)
Dosing
- Adult
- US: 3 mg/kg daily on days 1–5, 14, and 21 (total dose, 21 mg/kg). Asia: 10–15 mg/kg total dose. Africa: ~18 mg/kg total dose. Mediterranean/American regions: ≥20 mg/kg total dose. India: single dose of 10 mg/kg for VL elimination program. HIV/VL co-infection (Americas and Mediterranean): 40 mg/kg total dose, administered as 4 mg/kg on days 1–5, 10, 17, 24, 31, and 38.…
- Max dose
- Daily dose flexible (1–10 mg/kg).
Pharmacokinetics
Half-life
~150 h (terminal half-life, detectable in liver and spleen for several weeks after single dose)
Side effects
Common
infusion reactionsbackacheoccasional reversible nephrotoxicity
Related guidelines
Other Unclassified drugs
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Sources: Harrison 22e·Verified: 2026-05-13 · House clinical team