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The quality of sulphadoxine-pyrimethamine and amodiaquine products in the Kenyan retail sector.

机译:肯尼亚零售部门的磺胺多辛-乙胺嘧啶和阿莫二喹产品的质量。

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摘要

BACKGROUND AND OBJECTIVE: Malaria is a disease of major public health importance in Kenya killing 26,000 children under 5 years of age annually. This paper seeks to assess the quality of sulphadoxine-pyrimethamine (SP) and amodiaquine (AQ) products available over-the-counter to communities in Kenya as most malaria fevers are self-medicated using drugs from the informal retail sector. METHODS: A retail audit of 880 retail outlets was carried in 2002 in four districts in Kenya, in which antimalarial drug stocks and their primary wholesale sources were noted. In addition, the expiry dates on audited products and the basic storage conditions were recorded on a proforma. The most commonly stocked SP and AQ products were then sampled from the top 10 wholesalers in each district and samples subjected to standard United States Pharmacopoeia (USP) tests of content and dissolution. RESULTS AND DISCUSSION: SP and AQ were the most frequently stocked antimalarial drugs, accounting for approximately 75% of all the antimalarial drugs stocked in the four districts. Of 116 SP and AQ samples analysed, 47 (40.5%) did not meet the USP specifications for content and/or dissolution. Overall, approximately 45.3% of SP and 33.0% of AQ samples were found to be sub-standard. Of the sub-standard SP products, 55.2% were suspensions while 61.1% of the substandard AQ products were tablets. Most SP failures were because of the pyrimethamine component. CONCLUSION: There is a need to strengthen post-marketing surveillance systems to protect patients from being treated with sub-standard and counterfeit antimalarial drugs in Kenya.
机译:背景和目的:疟疾是肯尼亚重要的公共卫生疾病,每年造成26,000名5岁以下儿童死亡。本文旨在评估在肯尼亚社区可以通过非处方药获得的磺胺多辛-乙胺嘧啶(SP)和阿莫二喹(AQ)产品的质量,因为大多数疟疾热是使用非正规零售部门的药物自行治疗的。方法:2002年在肯尼亚的四个地区对880个零售店进行了零售审计,其中记录了抗疟药库存及其主要批发来源。此外,被审核产品的有效期和基本存储条件都记录在形式表中。然后从每个地区的前十名批发商中取样最常用的SP和AQ产品,并对样品进行含量和溶解度的标准美国药典(USP)测试。结果与讨论:SP和AQ是库存最多的抗疟药,约占四个地区所有库存抗疟药的75%。在分析的116种SP和AQ样品中,有47种(40.5%)不符合USP含量和/或溶出度标准。总体而言,发现约45.3%的SP和33.0%的AQ样品不合格。在不合格的SP产品中,悬浮液占55.2%,而不合格的AQ产品中片剂占61.1%。大多数SP故障是由于乙胺嘧啶成分所致。结论:有必要加强售后监测系统,以保护患者免于接受不合格和假冒抗疟药的治疗。

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