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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Dose-to-dose variations with single packages of counterfeit medicines and adulterated dietary supplements as a potential source of false negatives and inaccurate health risk assessments
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Dose-to-dose variations with single packages of counterfeit medicines and adulterated dietary supplements as a potential source of false negatives and inaccurate health risk assessments

机译:单一假药和掺假膳食补充剂的剂量之间的差异可能会导致假阴性和不正确的健康风险评估

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摘要

In this report, we show three examples of how the variability in dose units in single packages of counterfeit medicines and adulterated dietary supplements may contribute to a false negative screening result and inaccurate health risk assessments. We describe a counterfeit Viagra 100. mg blister pack and a box of an instant coffee both containing dose units with and without an active pharmaceutical ingredient (API). We also describe a purportedly herbal slimming product with capsules that mutually differed in API and impurities. The adulterated dietary supplements contained sibutramine, benzyl-sibutramine, N-desmethyl-sibutramine (DMS), N,N-didesmethyl-sibutramine (DDMS) and several other related impurities.Counterfeit medicines and adulterated dietary supplements are a health risk because their quality is unreliable. Health risks are even greater when such unreliability extends to fundamental differences between dose units in one package. Because dose-to-dose variability for these products is unpredictable, the confidence interval of a sample size is unknown. Consequently, the analyses of a selection of dose units may not be representative for the package. In the worst case, counterfeit or unauthorised medicines are not recognised as such or a health risk is not identified. In order to reduce erroneous results particular care should be taken when analysing a composite of dose units, when finding no API in a dietary supplement and when finding conformity in a suspect counterfeit medicine.
机译:在本报告中,我们展示了三个例子,说明假冒药品和掺假膳食补充剂的单包装中剂量单位的变化可能会导致假阴性筛查结果和不正确的健康风险评估。我们描述了一种假冒的伟哥100 mg泡罩包装和一盒速溶咖啡,都装有带有和不带有活性药物成分(API)的剂量单位。我们还描述了据称是草药减肥产品,其胶囊在API和杂质方面互不相同。 adult杂的膳食补充剂包含西布曲明,苄基西布曲明,N-去甲基-西布曲明(DMS),N,N-二去甲基西布曲明(DDMS)和其他几种相关杂质。假冒药品和adult杂的膳食补充剂的质量是不可靠。当这种不可靠性扩展到一个包装中剂量单位之间的根本差异时,健康风险就更大。由于这些产品的剂量间差异是不可预测的,因此样本量的置信区间未知。因此,剂量单位选择的分析可能无法代表包装。在最坏的情况下,仿冒或未经授权的药物不会被这样识别,也不会识别出健康风险。为了减少错误结果,在分析剂量单位的复合物,在膳食补充剂中未发现任何API以及在可疑假药中发现符合性时,应格外小心。

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