FDA Adverse Event Reporting System Database supports the FDA's post-marketing safety surveillance program for all marketed drug and therapeutic biologic products. It contains …

2023年12月7日 · While the FAERS dashboard offers stakeholders many more ways of searching for and organizing data on adverse events reported to the FDA for many drug and biologic …

The FDA Adverse Event Reporting System (FAERS) is a database that contains information on adverse event and medication error reports submitted to FDA. The database is designed to …

This image shows adverse events (AE) reports received by the FDA from 1999 to 2024. Data shown is as of September 30, 2024. The report types are as follows: Image from the U.S. …

MedWatch logo. MedWatch is the Food and Drug Administration’s “Safety Information and Adverse Event Reporting Program.” It interacts with the FDA Adverse Event Reporting System …

FDA Adverse Event Reporting System(FAERS) 全球最大的药物不良反应与不良事件自发上报信息公共数据库。 旨在支持美国食品和药物管理局 (FDA) 针对所有已批准药物和治疗性生物制品 …

The FAERS public dashboard is a new, user-friendly and interactive web-based tool that was created to give the public the ability to query the FDA FAERS database and improve …

FDA不良事件报告系统（FDA Adverse Event Reporting System，FAERS）是一个旨在支持FDA对药品和治疗性生物制品上市后监测计划的数据库，该数据库包括了FDA收集的所有不良事件信 …

FAERS 是一个用于监测和报告药物和医疗器械不良事件的重要数据库。 网址： fda.gov/drugs/drug-appr. 该系统旨在收集、分析和报告与药物使用相关的不良事件，为各位临 …

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