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meglumine antimoniate (Glucantime in France, Glucantim in Italy)

Indications: - cutaneous leishmaniasis Dosage: - parenteral (intravenous [2,3], intramuscular [1] - 20 mg/kg/day for 20 days [5] Adverse effects: - fever, rash, arthralgia, abdominal pain - skin eruption - pruritus and erythema in the site of injection - urticaria - pancreatic toxicity: hyperamylasemia, increased serum lipase - increased serum transaminases - pancytopenia - renal failure, hepatic failure, death Notes: - lower efficacy in treating cutaneous leishmaniasis in children than adults [5]

General

antiprotozoal agent

References

  1. Wikipedia: Meglumine antimoniate http://en.wikipedia.org/wiki/Meglumine_antimoniate
  2. Mayo Clinic Meglumine Antimoniate (Intravenous Route, Injection Route). http://www.mayoclinic.org/drugs-supplements/meglumine-antimoniate-intravenous-route-injection-route/description/drg-20064644
  3. Ezzine Sebai N1, Mrabet N, Khaled A et al [Side effects of meglumine antimoniate in cutaneous leishmaniasis: 15 cases]. Tunis Med. 2010 Jan;88(1):9-11. PMID: 20415206
  4. Roberts WL et al Characterization of the Antimonial Antileishmanial Agent Meglumine Antimonate (Glucantime). Antimicrob Agents Chemother. May 1998; 42(5): 1076-1082. PMID: 9593130 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC105748/
  5. Layegh P, Rahsepar S, Rahsepar AA. Systemic meglumine antimoniate in acute cutaneous leishmaniasis: children versus adults. Am J Trop Med Hyg. 2011 Apr;84(4):539-42. doi: 10.4269/ajtmh.2011.10-0002. PMID: 21460006