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Quality Assessment of Some Essential Children’s Medicines Sold in Licensed Outlets in Ashanti Region, Ghana

机译:加纳阿散蒂地区许可出口销售的某些基本儿童药物的质量评估

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The quality of 68 samples of 15 different essential children’s medicines sold in licensed medicine outlets in the Ashanti Region, Ghana, was evaluated. Thirty-two (47.1%) of the medicines were imported, mainly from India (65.6%) and the United Kingdom (28.1%), while 36 (52.9%) were locally manufactured. The quality of the medicines was assessed using content of active pharmaceutical ingredient (API), pH, and microbial limit tests, and the results were compared with pharmacopoeial standards. Twenty-six (38.2%) of the samples studied passed the official content of API test while 42 (61.8%) failed. Forty-nine (72.1%) of the samples were compliant with official specifications for pH while 19 (27.9%) were noncompliant. Sixty-six (97.1%) samples passed the microbial load and content test while 2 (2.9%) failed. Eighteen (26.5%) samples passed all the three quality evaluation tests, while one (1.5%) sample (CFX1) failed all the tests. All the amoxicillin suspensions tested passed the three evaluation tests. All the ciprofloxacin, cotrimoxazole, flucloxacillin, artemether-lumefantrine, multivitamin, and folic acid samples failed the content of API test and are substandard. The overall API failure rate for imported products (59.4%) was comparable to locally manufactured (63.9%) samples. The results highlight the poor quality of the children’s medicines studied and underscore the need for regular pharmacovigilance and surveillance systems to fight this menace.
机译:我们评估了加纳阿散蒂地区有执照的药店出售的15种基本儿童药的68种样品的质量。其中32种药品(47.1%)是进口的,主要从印度(65.6%)和英国(28.1%)进口,而36种药品(52.9%)是本地生产的。使用活性药物成分(API)的含量,pH值和微生物限量测试评估了药物的质量,并将结果与​​药典标准进行了比较。 26个样本(38.2%)通过了API测试的官方内容,而42个样本(61.8%)不及格。其中有49个样品(占72.1%)符合官方的pH要求,而19个样品(占27.9%)不符合要求。 66(97.1%)个样品通过了微生物负荷和含量测试,而2个(2.9%)不通过。 18个(26.5%)样品通过了所有三个质量评估测试,而一个(1.5%)样品(CFX1)未通过所有测试。所有测试的阿莫西林悬浮液均通过了三个评估测试。所有环丙沙星,cotrimoxazole,氟氯西林,蒿甲醚-萤石碱,多种维生素和叶酸样品均未通过API测试,不合格。进口产品的总体API失效率(59.4%)与本地制造的样品(63.9%)相当。研究结果突显了所研究儿童药物的质量较差,并强调需要定期的药物警戒和监测系统来应对这种威胁。

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