Serious adverse events by randomisation arm.

Figshare2018-11-27 更新2026-04-29 收录

临床试验安全性

不良事件分析

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资源简介：

Serious adverse events by randomisation arm.

创建时间：

2018-11-27

Adverse events in patients taking macrolide antibiotics versus placebo for any indication: Supplementary data set B

用药安全

不良事件分析

Supplementary data B Any reported adverse event that occurred in less than 5% of any group – grouped under the primary System Organ Class, according to the MedDRA coding system.

Research Data Australia80

Number of patients (total = 57) with clinical adverse effects (chi-square test with Yates correction).

不良事件分析

药物安全性评估

Number of patients (total = 57) with clinical adverse effects (chi-square test with Yates correction).

NIAID Data Ecosystem60

Correlations between frequency of adverse events reported and patient safety culture.

安全文化评估

不良事件分析

Correlations between frequency of adverse events reported and patient safety culture.

Figshare2022-10-19 更新50

RETRACTED ARTICLE: Clinical adverse events to letairis: a real-world drug safety study based on FDA Adverse Event Reporting System (FAERS)

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RETRACTED ARTICLE: Clinical adverse events to letairis: a real-world drug safety study based on FDA Adverse Event Reporting System (FAERS)

DataCite Commons2026-01-02 更新70

Disproportionality Analysis of Fondaparinux-Associated Adverse Events Based on the FDA Adverse Event Reporting System (FAERS)

药物安全

不良事件分析

This dataset contains the minimal underlying data used to reproduce the findings of the study titled “Safety profile of fondaparinux based on the FAERS database: a disproportionality analysis”. The da

DataCite Commons2025-11-16 更新60

Serious adverse events by randomisation arm.

资源简介：

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