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心血管类药物的药物不良反应——保加利亚人群的数据

Adverse Drug Reactions of Cardiovascular Classes of Medicines-Data for Bulgarian Population.

作者信息

Mitkova Zornitsa, Dimova Anita, Petrova Guenka, Dimitrova Maria

机构信息

Faculty of Pharmacy, Medical University-Sofia, 1000 Sofia, Bulgaria.

出版信息

Biomedicines. 2024 Sep 24;12(10):2163. doi: 10.3390/biomedicines12102163.

Abstract

Hypertensionis one of the most common chronic diseases, affecting more than 20% of the population. The side effects experienced due to antihypertensive medications, such as tiredness, muscle pain, and insomnia, are often a significant predictor of poor adherence to therapy. The goal of the current study is to present the frequency, type, seriousness, and severity of adverse drug reactions reported to the BDA via Individual Case Safety Reports (ICSRs) and following differentiation of messages found in more than one patient. We conducted a retrospective analysis of the reported adverse drug reactions (ADRs) reported in the Bulgarian Drug Agency database after treatment with antihyperlipidemic medicines, angiotensin-converting enzyme (ACE) inhibitors, and sartans for the period 2017-2021. Each ICSR form was observed, and data for suspected medicine and type of adverse reaction was analyzed. The total number of processed notifications for adverse drug reactions (ADRs) included in the database is 142. The highest number of ADRs was reported for ARB (58), followed by antihyperlipidemic medicines (55) and ACE inhibitors (29). Most of the assessed adverse events experienced by more than one patient fall into the probable and related categories based on the Global Introspection method classification. Therefore, they have been investigated and are consistent with exposure in the population. Cardiovascular medicines from the groups of ACE inhibitors, sartans, and statins have a high share of reported ADRs in the BDA system. Some of them are severe and need further investigation.

摘要

高血压是最常见的慢性病之一,影响着超过20%的人口。抗高血压药物所带来的副作用,如疲劳、肌肉疼痛和失眠,往往是治疗依从性差的重要预测指标。本研究的目的是通过个体病例安全报告(ICSR)以及对多名患者中发现的信息进行区分,呈现向保加利亚药品局报告的药物不良反应的频率、类型、严重性和程度。我们对保加利亚药品局数据库中2017 - 2021年期间使用抗高脂血症药物、血管紧张素转换酶(ACE)抑制剂和沙坦类药物治疗后报告的药物不良反应(ADR)进行了回顾性分析。观察了每份ICSR表格,并分析了可疑药物和不良反应类型的数据。数据库中处理的药物不良反应(ADR)通知总数为142份。报告的ADR数量最多的是ARB(58例),其次是抗高脂血症药物(55例)和ACE抑制剂(29例)。根据全球内省法分类,多名患者经历的大多数评估不良事件属于“可能”和“相关”类别。因此,它们已经过调查且与人群中的暴露情况一致。ACE抑制剂、沙坦类和他汀类药物组中的心血管药物在保加利亚药品局系统中报告的ADR占比很高。其中一些不良反应很严重,需要进一步调查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f7b/11504719/9e536a3ae98c/biomedicines-12-02163-g001.jpg

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