Sunara Petra, Krnic Darko, Puljak Livia
Laboratory for Pain Research, University of Split School of Medicine, Split, Croatia.
Agency for Medicinal Products and Medical Devices, Zagreb, Croatia.
Acta Med Acad. 2017 Nov;46(2):94-104. doi: 10.5644/ama2006-124.194.
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.
HALMED provided data on generic drug name, year of the ADR report, type of report, institution, reporting person, patient's age, sex and ADR type.
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 reports of those 20 analgesics referred to individual drugs (n=16; 80%). Most of the ADR reports were filed by physicians (n=257; 43%), followed 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 women (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.
Number of ADR reports in Croatia is continuously increasing and a considerable 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.
由于系统缺陷和个人失误,药物不良反应(ADR)在医疗服务中很常见。镇痛药被广泛使用,预计随着使用量的增加,镇痛药的ADR数量也会增加。本研究的目的是分析2007年至2014年向克罗地亚药品和医疗器械局(HALMED)报告的非阿片类和阿片类镇痛药的ADR。
HALMED提供了通用药品名称、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。
在分析期间,共报告了796例镇痛药ADR,其中367例(46%)为严重ADR。在分析期间,ADR报告数量持续增加。有20种镇痛药报告≥5例,占镇痛药所有ADR报告的597例(75%)。这20种镇痛药最常见的不良反应报告涉及个别药物(n = 16;80%)。大多数ADR报告由医生提交(n = 257;43%),其次是药剂师(n = 252;42%)。大多数副作用(n = 572;96%)是由患者或卫生专业人员通过适当表格自发报告的。ADR最常报告于女性(n = 352;59%),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报告于皮肤和粘膜。大多数严重ADR是阿片类镇痛药作用的结果。
克罗地亚的ADR报告数量持续增加,其中相当一部分涉及严重ADR。为了更好地跟踪药物和ADR,有必要教育和鼓励卫生专业人员及患者报告副作用。