Identification and comparison of sex-specific serious adverse drug reactions in spontaneous reports and systematically collected reports (ADRED)

IF 3 3区 医学 Q2 PHARMACOLOGY & PHARMACY British journal of clinical pharmacology Pub Date : 2023-10-27 DOI:10.1111/bcp.15941
Patrick Christ, Diana Dubrall, Katja Susanne Just, Britta Lewke, Maike Below, Julia Carolin Stingl, Matthias Schmid, Bernhardt Sachs
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Abstract

Aims

Adverse drug reactions (ADRs) are known to show sex-specific differences in occurrence and phenotype. The aim of this study was to analyse sex-specific differences in ADR–drug combinations that required hospitalization based on two different datasets.

Methods

We performed a complementary analysis of (i) spontaneously reported (n = 12 564, female = 51.7%) and (ii) systematically collected ADR reports from a prospective multicentre observational study (ADRED, n = 2355, female = 48.2%) from Germany in the ADR database EudraVigilance (EV). Both datasets were analysed separately concerning the suspected drugs, ADRs and ADR–drug combinations more frequently reported for females or males by calculating reporting odds ratios (ROR) with 95% confidence intervals. ADR–drug combinations more frequently reported for either females or males in EV reports were related to prescription data. Finally, the results from both datasets were discussed with regard to their (dis-)concordance.

Results

In both datasets, some antineoplastic agents and nervous system drugs were found to be reported more often for females than males (RORs ranging from 1.5 [1.1–2.1] for quetiapine in spontaneous reports to 41.3 [13.1–130.0] for trastuzumab in spontaneous reports). ADRs of the respiratory system, and haemorrhages were described predominantly for males in both datasets. In spontaneous reports the ADR–drug combination self-injurious behaviour–quetiapine was more often reported for females without and with consideration of drug prescriptions (ROR: 3.8 [1.3–11.0]). Quetiapine and psychiatric disorders (superordinate level) was exclusively reported for females in ADRED reports.

Conclusions

Our results can contribute to raise awareness and further knowledge regarding sex-specific ADRs. The findings require further in-depth investigation.

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自发报告和系统收集报告中性别特异性严重药物不良反应的识别和比较(ADRED)。
目的:已知药物不良反应(ADR)在发生率和表型上表现出性别特异性差异。本研究的目的是基于两个不同的数据集分析需要住院治疗的ADR药物组合的性别特异性差异。方法:我们对i)自发报告的(n=12564,女性=51.7%)和ii)在ADR数据库EudraVigilance(EV)中从德国前瞻性多中心观察性研究(ADRED,n=2355,女性=48.2%)系统收集的ADR报告进行了补充分析。通过计算95%置信区间(CI)的报告优势比(ROR),分别分析了两个数据集,涉及女性或男性更频繁报告的可疑药物、ADR和ADR药物组合。EV报告中女性或男性更频繁报告的ADR药物组合与处方数据有关。最后,讨论了两个数据集的结果的一致性/不一致性。结果:在这两个数据集中,发现一些抗肿瘤药物和神经系统药物在女性中的报告频率高于男性(ROR范围为1.5[1.1-21](喹硫平EV)至41.3[113.1-130.0](曲妥珠单抗EV))。在这两个数据集中,主要描述了男性的呼吸系统ADR和出血。在EV中,在没有药物处方或考虑药物处方的情况下,女性更常报告ADR药物组合自伤行为-喹硫平(ROR:3.8[1.3-11.0])。在ADR报告中,女性仅报告喹硫平和精神障碍(上级)。结论:我们的研究结果有助于提高对性别特异性ADR的认识和进一步了解。调查结果需要进一步深入调查。
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来源期刊
CiteScore
6.30
自引率
8.80%
发文量
419
审稿时长
1 months
期刊介绍: Published on behalf of the British Pharmacological Society, the British Journal of Clinical Pharmacology features papers and reports on all aspects of drug action in humans: review articles, mini review articles, original papers, commentaries, editorials and letters. The Journal enjoys a wide readership, bridging the gap between the medical profession, clinical research and the pharmaceutical industry. It also publishes research on new methods, new drugs and new approaches to treatment. The Journal is recognised as one of the leading publications in its field. It is online only, publishes open access research through its OnlineOpen programme and is published monthly.
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