Table 3. The main drugs currently used for treatment of visceral leishmaniasis.
Drug | Regimen | Toxicity | Cost/coursea | Main issues |
Pentavalent Antimonials | 20 mg/Sb5+/kg iv or im daily for 28–30 days | Frequent, potentially severe; Pancreatitis; Cardio, nephro hepatotoxicity | Generic ∼$53 Branded $70 | Length of treatment Painful injection Toxicity: high mortality in co-infected African Patients Resistance in India |
Conventional Amphotericin B | 0.75–1 mg/kg iv for 15–20 doses (daily or alternate days) | Frequent Infusion-related Reactions, Nephrotoxicity | Generic price: ∼$21 | Lengthy hospitalisation (in-patient care) Need for slow iv infusion Toxicity Heat stability |
Liposomal Amphotericin B | 3–5 mg/kg/d iv up to total dose of 10–30 mg/kg Single dose (10 mg/kg) in India | Uncommon and mild; Nephrotoxicity (limited) | Preferential price: $280 (20 mg/kg total dose) Commercial price: ∼10× | Price Slow iv infusion Heat stability (<25°C) Single dose not effective in East Africa |
Miltefosine | Orally daily over 28 days; dose according to age and body weight | Common, usually mild and transient; gastro-intestinal, Nephro + Hepatotoxicity Possibly teratogenic | Preferential price: ∼$74 Commercial price: ∼$150 | Price Possibly teratogenic Potential for resistanceb Patient compliance Relatively limited efficacy data in East Africa |
Paromomycin Sulphate | 15 mg/kg im daily for 21 Days (Indian subcontinent) | Uncommon, Nephrotoxicity Ototoxicity Hepatotoxicity | ∼$15 | Efficacy variable between and within regions (less in Sudan) Resistance readily obtained in lab isolates |
Actual costs of the drugs, costs related to the logistics of storage and distribution are not taken into consideration.
Due to long half-life + low genetic barrier (resistance readily obtained in lab isolates).
iv: intravenous; im: intramuscular.