Management and outcome of the reported adverse events.

Figshare2016-09-28 更新2026-04-29 收录

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Management and outcome of the reported adverse events.

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2016-09-28

Table 2_Drug-induced kidney stones: a real-world pharmacovigilance study using the FDA adverse event reporting system database.xlsx

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药物诱导肾结石风险

ObjectiveThis study aims to identify the drugs most commonly associated with kidney stone-related adverse events using data from the FDA Adverse Event Reporting System (FAERS), providing insights for

NIAID Data Ecosystem70

A real-world pharmacovigilance study of FDA adverse event reporting system (FAERS) for gemcitabine

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抗癌药物安全性

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30

Supplementary file 1_Real-world safety profile of roflumilast: a pharmacovigilance analysis using FDA adverse event reporting system and Canada vigilance database.docx

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BackgroundRoflumilast, a highly selective phosphodiesterase 4 inhibitor, is used to treat with chronic obstructive pulmonary disease and psoriasis. We aim to determine potential roflumilast-associated

NIAID Data Ecosystem10

Main characteristics of adverse events (AE) rates.

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Main characteristics of adverse events (AE) rates.

NIAID Data Ecosystem50

Table_1_Lung Cancer Adverse Events Reports for Angiotensin-Converting Enzyme Inhibitors: Data Mining of the FDA Adverse Event Reporting System Database.docx

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不良反应信号检测

Because of contradictory evidence from clinical trials, the association between angiotensin-converting enzyme inhibitors (ACEIs) and lung cancer needs further evaluation. As such, the current study is

NIAID Data Ecosystem30

Management and outcome of the reported adverse events.

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