Objective: To mine the adverse drug event (ADE) signals of upadacitinib based on the Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) database to provide a reference for the safe clinical use of the drug. Methods: The ADE data for upada...
Methods The US FDA Adverse Event Reporting System database was searched, and the AE reports on MMF as the primary suspect drug from the 1st quarter of 2004 to the 3rd quarter of 2022 were collected. AEs were counted and classified using the preferred system organ class (SOC) and preferred ...
Methods The US FDA Adverse Event Reporting System database was searched and AE reports on brigatinib as the primary suspect drug from April 1, 2017 to March 31, 2022 were collected. AEs were standardized and classified according to the preferred terms (PT) and system organ class (SOC) of...
Novel Adverse Events of Bevacizumab in the US FDA Adverse Event Reporting System Database: A Disproportionality Analysis Novel adverse events of bevacizumab in the US FDA adverse event reporting system database: a disproportionality analysis. Drug Saf. 35(6), 507-518 (... Shamloo,Behrooz,K.,....
FDA Adverse Event Reporting System (FAERS) Quarterly Data Files FDA不良事件报告系统(FAERS)季度数据文件Downloadable data files. 可下载的数据文件 FDA Adverse Event Reporting System (FAERS) Public Dashboard FDA不良事件报告系统(FAERS)公告板 Inactive Ingredient Search for Approv...
TITLE: ADR Signal Mining of Rivaroxaban Based on FDA Adverse Event Reporting Database 摘要: 目的:挖掘利伐沙班的药品不良反应(ADR)信号,为其临床安全合理使用提供参考。方法:基于美国FDA不良事件报告系统,采用报告比值比法和比例报告比法对FDA公共数据开放项目中于2008年9月-2020年12月上报的利伐沙班ADR报告进行...
Dissolution Methods Database Search:溶出方法数据库搜索 如上图所示,溶出方法可通过至少3个关键词直接查询,查询的结果包括装置、转速、介质、介质体积、取样点等信息,内容非常全面。 Drug Establishments Current Registration Site Search药品经营机构现行注册网站查询 ...
This study aimed to evaluate the presence of cardiovascular safety signals with currently marketed antiobesity drugs.We used the US Food and Drug Administration Adverse Event Reporting System (FAERS) database and retrieved data from January 2013 through December 2018. We performed disproportionality ...
The Safety RatesDrugReport This website provides free access to alladverse events(problem reports, such as heart attacks, strokes, cancer, etc.) data submitted to the FAERS (FDA Adverse Event Reporting System) database forprescription drugs.In the next phase, this will include new search capabil...
Can the FDA's Adverse Event Reporting System (FAERS) Data Be Used to Assess the Impact of interventions Such As Risk Evaluation and Mitigation Strategies (... Based on the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS) database, we analyzed the signals of potential...