首页/数据集/Source of information and responsible person for PV and ADR reporting (n = 412).

Source of information and responsible person for PV and ADR reporting (n = 412).

NIAID Data Ecosystem2026-05-01 收录

数据链接：

https://figshare.com/articles/dataset/Source_of_information_and_responsible_person_for_PV_and_ADR_reporting_n_412_/23149852 数据链接链接失效反馈

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Source of information and responsible person for PV and ADR reporting (n = 412).

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创建时间：

2023-05-24

药物警戒

医疗器械不良反应

FDA不良事件报告系统公共仪表板是美国食品药品监督管理局(FDA)维护的数据库，用于收集和公开药品、生物制品和医疗器械的不良事件报告。该系统提供实时数据可视化，帮助医疗专业人员、研究人员和公众了解药物安全性和潜在风险。数据库包含来自医疗保健专业人员、消费者和制造商的自愿报告信息。

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药物警戒

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Previous studies have explored the association between levetiracetam (LEV) and severe cutaneous adverse reactions (SCARs). However, most investigations have relied on clinical trial data or case repor

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A real-world pharmacovigilance study of FDA Adverse Event Reporting System (FAERS) for gemcitabine

药物警戒

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Gemcitabine is widely used in the treatment of various cancers. This study aims to evaluate gemcitabine-associated adverse events (AEs) using the Food and Drug Administration Adverse Event Reporting S

Taylor & Francis Group2025-03-13 更新40

BCG-associated death AE case reports from VAERS.

疫苗安全监测

药物警戒

BCG-associated death AE case reports from VAERS.

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Drug-induced skin ulcer: real-world pharmacovigilance analysis based on the FDA adverse event reporting system

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药物警戒

Skin ulcer (SU) may increase the risk of systemic infections and have evolved into an important public health problem. However, there is a lack of research specifically on drug-induced SU. We extracte

Taylor & Francis Group2025-05-14 更新40

Source of information and responsible person for PV and ADR reporting (n = 412).

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