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Retrospective Study of Reported Adverse Events Due to Complementary Health Products in Singapore From 2010 to 2016

机译:2010年至2016年新加坡补充保健品引起的不良事件报道的回顾性研究

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摘要

The objective of this study is to collate and analyse adverse event reports associated with the use of complementary health products (CHP) submitted to the Health Sciences Authority (HSA) of Singapore for the period 2010–2016 to identify various trends and signals for pharmacovigilance purposes. A total of 147,215 adverse event reports suspected to be associated with pharmaceutical products and CHP were received by HSA between 2010 and 2016. Of these, 143,191 (97.3%) were associated with chemical drugs, 1,807 (1.2%) with vaccines, 1,324 (0.9%) with biological drugs (biologics), and 893 (0.6%) with CHP. The number of adverse event reports associated with Chinese Proprietary Medicine, other complementary medicine and health supplements are presented. Eight hundred and ninety three adverse event reports associated with CHP in the 7-year period have been successfully collated and analyzed. In agreement with other studies, adverse events related to the “skin and appendages disorders” were the most commonly reported. Most of the cases involved dermal allergies (e.g., rashes) associated with the use of glucosamine products and most of the adulterated products were associated with the illegal addition of undeclared drugs for pain relief. Dexamethasone, chlorpheniramine, and piroxicam were the most common adulterants detected. Reporting suspected adverse events is strongly encouraged even if the causality is not confirmed because any signs of clustering will allow rapid regulatory actions to be taken. The findings from this study help to create greater awareness on the health risks, albeit low, when consuming CHP and dispelling the common misconception that “natural” means “safe.” In particular, healthcare professionals and the general public should be aware of potential adulteration of CHP. The analysis of spontaneously reported adverse events is an important surveillance system in monitoring the safety of CHP and helps in the understanding of the risk associated with the use of such products. Greater collaboration and communication between healthcare professionals, regulators, patients, manufacturers, researchers, and the general public are important to ensure the quality and safety of CHP.
机译:这项研究的目的是整理和分析与使用补充保健品(CHP)相关的不良事件报告,该报告已提交给新加坡卫生科学局(HSA),于2010-2016年期间进行,以识别药物警戒目的各种趋势和信号。 HSA在2010年至2016年期间共收到147,215例疑似与药品和CHP有关的不良事件报告。其中143,191例(97.3%)与化学药品有关,1,807例(1.2%)与疫苗相关,1,324例(0.9) %的生物药物(生物制剂)和893(0.6%)的CHP。介绍了与中成药,其他辅助药物和保健补品相关的不良事件报告的数量。已成功整理和分析了7年内与CHP相关的893例不良事件报告。与其他研究一致,与“皮肤和阑尾疾病”有关的不良事件是最常报告的。大多数病例涉及与使用氨基葡萄糖产品有关的皮肤过敏(例如皮疹),大多数掺假产品与非法添加未申报的药物有关,以减轻疼痛。地塞米松,扑尔敏和吡罗昔康是最常见的掺杂物。即使未确认因果关系,也强烈建议报告可疑不良事件,因为任何聚类迹象都将允许采取迅速的监管措施。这项研究的发现有助于人们在消费CHP并消除人们普遍认为“自然”意味着“安全”的误解时,尽管对健康的危害却很小。尤其是,医疗保健专业人员和公众应该意识到CHP可能被掺假。自发报告的不良事件的分析是监测CHP安全性的重要监视系统,有助于理解与使用此类产品相关的风险。卫生保健专业人员,监管机构,患者,制造商,研究人员和公众之间加强合作与沟通对于确保CHP的质量和安全至关重要。

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