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Hematoxicity of Amodiaquine in Sprague-Dawley Rats

OBJECTIVE: The use of amodiaquine (AQ) and its associated toxic effect has been a major public health concern since cases of life-threatening agranulocytosis and hepatic toxicity were reported during its prophylactic use. The objective of this study was to evaluate the hematological safety profile o...

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Detalles Bibliográficos
Autores principales: Saka, W. A., Akhigbe, R. E., Akinola, A. O., Azeez, O. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388752/
https://www.ncbi.nlm.nih.gov/pubmed/22778506
http://dx.doi.org/10.4103/0971-6580.97197
Descripción
Sumario:OBJECTIVE: The use of amodiaquine (AQ) and its associated toxic effect has been a major public health concern since cases of life-threatening agranulocytosis and hepatic toxicity were reported during its prophylactic use. The objective of this study was to evaluate the hematological safety profile of AQ therapy. MATERIALS AND METHODS: Sprague-Dawley rats were randomly distributed into four groups (n=5). Group 1 was the control, while groups 2, 3, and 4 received AQ treatment for 14 days at varying doses of 5 mg/kgBW, 10 mg/kgBW, and 15 mg/kgBW daily, respectively. RESULTS: Following treatment, hematological variables were comparable in all groups (P>0.05). CONCLUSION: This study provides evidence to support the use of AQ in the treatment of uncomplicated malaria. However, to prevent emergence of local drug resistance, it should be used as part of a combination therapy. Monitoring for adverse effects is suggested.