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Adverse metabolic effects of antiparasitic drugs.

Abstract
Several drugs are available for mass campaigns against enteric helminths. Mebendazole and pyrantel pamoate are quite effective against ascariasis and reasonably effective against the hookworms. Only mebendazole is effective against trichuriasis. Two drugs have recently been introduced for mass therapy of schistosomiasis, but they remain experimental, pending further evaluation. Other drugs are mentioned, and possible adverse metabolic effects are discussed. The fundamental question remaining is whether the eradication of certain parasites will improve the nutritional status of the infected populations.
AuthorsM Katz
JournalReviews of infectious diseases (Rev Infect Dis) 1982 Jul-Aug Vol. 4 Issue 4 Pg. 768-70 ISSN: 0162-0886 [Print] United States
PMID6750743 (Publication Type: Journal Article, Review)
Chemical References
  • Anthelmintics
  • Oxamniquine
  • Pyrantel Pamoate
  • Mebendazole
  • DDT
  • Thiabendazole
Topics
  • Animals
  • Anthelmintics (adverse effects, therapeutic use)
  • DDT (adverse effects)
  • Giardiasis (complications, drug therapy, metabolism)
  • Helminthiasis (complications, drug therapy, metabolism)
  • Humans
  • Malaria (complications, drug therapy, metabolism)
  • Mebendazole (adverse effects, therapeutic use)
  • Nutrition Disorders (complications)
  • Oxamniquine (adverse effects, therapeutic use)
  • Oxyuriasis (drug therapy, metabolism)
  • Pyrantel Pamoate (adverse effects, therapeutic use)
  • Rabbits
  • Schistosomiasis (drug therapy, metabolism)
  • Strongyloidiasis (drug therapy, metabolism)
  • Thiabendazole (adverse effects, therapeutic use)

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