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Adverse drug reactions of non-opioid and opioid analgesics reported to Croatian national authority from 2007 to 2014

机译:2007年至2014年间向克罗地亚国家主管部门报告了非阿片类药物和阿片类镇痛药的不良药物反应

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Objective. Adverse drug reactions (ADRs) are commonly observed in the health services because of system weaknesses and individual errors. Analgesics are widely used and it can be expected that with the increased use one can expect increased number of ADRs of analgesics. The aim of this study was to analyze ADRs of non-opioid and opioid analgesics reported to the Croatian Agency for Medicinal Products and? Medical Devices (HALMED) from? 2007? to 2014.? Methods. HALMED provided data on generic drug name, year of the ADR re- port, type of report, institution, reporting person, patient’s age, sex and ADR type. Results. In the analyzed period 796 ADRs of analgesics were reported, of which 367 (46%) were serious ADRs. Number of ADR reports was continuously increasing during the analyzed period. There were 20 analgesics that had ≥5 reports, making 597 (75%) of all ADR reports for analgesics. The most common adverse reaction re- ports of those 20 analgesics referred to individual drugs (n=16; 80%). Most of the ADR reports were filed by physicians (n=257; 43%), fol- lowed by pharmacists (n=252; 42%). Most side effects (n=572; 96%) were reported spontaneously through appropriate forms by patients or health professionals. ADRs were most commonly reported in wom- en (n=352; 59%) and most of them have occurred in adults (n=354; 59%). The most common ADRs of opioid and non-opioid analgesics have been reported on the skin and mucous membranes. Most serious ADRs were result of action of opioid analgesics. Conclusion. Num- ber of ADR reports in Croatia is continuously increasing and a consid- erable number of them refers to serious ADRs. To keep better track of medications and ADRs it is necessary to educate and encourage health professionals and patients in reporting side effects
机译:目的。由于系统弱点和个人错误,在医疗服务部门通常会观察到药物不良反应(ADR)。止痛药被广泛使用,可以预期随着使用量的增加,止痛药的ADR数量会增加。这项研究的目的是分析向克罗地亚药品管理局报告的非阿片类药物和阿片类镇痛药的ADR。医疗设备(HALMED)来自哪里? 2007年?到2014年。方法。 HALMED提供了有关通用药品名称,ADR报告年份,报告类型,机构,报告人,患者年龄,性别和ADR类型的数据。结果。在分析期内,报告了796种止痛药ADR,其中367种(46%)是严重的ADR。在分析期间,ADR报告的数量持续增加。有20多种镇痛药的报告≥5,占所有ADR镇痛药报告的597例(占75%)。在这20种镇痛药中,最常见的不良反应报告涉及个别药物(n = 16; 80%)。大部分ADR报告由医师提交(n = 257; 43%),其次是药剂师(n = 252; 42%)。大多数副作用(n = 572; 96%)由患者或医护人员通过适当形式自发报告。在女性中最常见的是ADR(n = 352; 59%),而且大多数发生在成年人中(n = 354; 59%)。阿片类和非阿片类镇痛药最常见的ADR已在皮肤和粘膜上报道。最严重的不良反应是阿片类镇痛药作用的结果。结论。克罗地亚的ADR报告数量在不断增加,其中相当多的报告涉及严重的ADR。为了更好地跟踪药物和ADR,必须教育和鼓励卫生专业人员和患者报告副作用

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