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Clinical outcomes by randomised arm.

Figshare2015-12-03 更新2026-04-29 收录

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https://figshare.com/articles/dataset/_Clinical_outcomes_by_randomised_arm_/1320212 数据链接链接失效反馈

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资源简介：

*Grade 3/4 adverse events summarised by MedDRA System Organ Class which were reported by 5 or more peoplepy: person yearsClinical outcomes by randomised arm.

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创建时间：

2015-12-03

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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

A real-world disproportionality analysis of ospemifene: data mining of the public version of FDA adverse event reporting system

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Ospemifene has been authorized for the treatment of vulvovaginal atrophy (VVA). This study wasto evaluate adverse events (AEs) associated with ospemifene by data mining the US Food and Drug Administra

DataCite Commons2024-02-27 更新60

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

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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

RETRACTED ARTICLE: Clinical adverse events to letairis: a real-world drug safety study based on FDA Adverse Event Reporting System (FAERS)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RETRACTED ARTICLE: Clinical adverse events to letairis: a real-world drug safety study based on FDA Adverse Event Reporting System (FAERS)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

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

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

NIAID Data Ecosystem60