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Spontaneously Reported Adverse Reactions for Herbal Medicinal Products and Natural Remedies in Sweden 2007–15: Report from the Medical Products Agency

机译:瑞典自发报告的草药和自然疗法的不良反应2007-15:医疗产品管理局的报告

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BackgroundIn relation to the extensive use of herbal medicinal products in self-care, the safety information is limited and there is a need for improvement. This study describes spontaneously reported adverse reactions related to herbal medicinal products and natural remedies in Sweden. ObjectivesTo evaluate the characteristics and frequency of adverse events recorded by the Swedish Medical Products Agency, where herbal medicinal products and natural remedies were suspected as causative agents. MethodsAdverse drug reactions reported to the Swedish Medical Product Agency during 2007–15 related to approved herbal medicinal products or natural remedies were included and analysed in the retrospective study. Reports had been assessed for causality when they were lodged and only reports that had been assessed as at least possible were included in the study. ResultsIn total, 116 reports (concerning 259 adverse reactions) related to herbal medicinal products or natural remedies were found in the Swedish national pharmacovigilance database. The active ingredients most frequently suspected during the study period were black cohosh rhizome (15 reports), purple coneflower herb (14 reports) and a combination of extracts of pollen (13 reports). Adverse reactions related to skin and subcutaneous tissue were the most commonly reported reactions. ConclusionsNo previously unknown safety problems have been discovered in the present study. This finding could be explained by a thorough pre-approval assessment of medicinal products and the fact that most herbal preparations in medicinal products have been in clinical use for many years (for traditional herbal medicinal products, the requirements are ≥30 years), i.e. adverse reactions are acknowledged and assessed before approval.
机译:背景技术关于在自我护理中广泛使用草药产品,安全性信息有限,需要改进。这项研究描述了瑞典自发报道的与草药和自然疗法有关的不良反应。目的评估瑞典医疗产品局记录的不良事件的特征和发生频率,瑞典医疗产品局怀疑其中草药和天然药物为病原体。方法回顾性研究纳入2007-15年度向瑞典医疗产品管理局报告的与批准的草药产品或天然药物有关的不良药物反应,并进行了分析。提交报告时已对它们进行了因果关系评估,并且仅将已被评估为至少可能的报告纳入研究。结果在瑞典国家药物警戒数据库中共发现116份与草药或自然疗法有关的报告(关于259不良反应)。在研究期间最常被怀疑的活性成分是黑升麻根茎(15份报告),紫色锥花药草(14份报告)和花粉提取物的组合(13份报告)。与皮肤和皮下组织有关的不良反应是最常见的反应。结论在本研究中未发现以前未知的安全问题。这一发现可以通过对药品的全面预先批准评估以及以下事实来解释:药品中的大多数草药制剂已经投入临床使用多年(对于传统草药,要求≥30年),即不良在批准之前确认并评估反应。

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