FDA Medical Device Adverse Events

kaggle2025-09-25 更新2025-10-25 收录

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资源简介：

MAUDE report sample with event details and dates

创建时间：

2025-09-25

Data and Code for "Late adverse event reporting from medical device manufacturers to the FDA: cross sectional study"

These files represent the needed data and code to reconstruct all figures presented in "Late adverse event reporting from medical device manufacturers to the FDA: cross sectional study." In order to r

Mendeley Data20

Medical Device Adverse Events for Total Hip Replacements

**Overview** This accelerator contains report on Adverse Events Total Hip Replacement for year 2014, 2015 and 2016. **Description** Each year, the FDA receives several hundred thousand medical devic

Databricks40

Data and Code for "Late adverse event reporting from medical device manufacturers to the FDA: cross sectional study"

Mendeley Data10

Data and Code for "Late adverse event reporting from medical device manufacturers to the FDA: cross sectional study"

DataCite Commons2025-04-01 更新50

FDA AEMS Adverse Events Dataset

# Overview The **FDA AEMS Adverse Events Dataset** unifies **23M+ U.S. FDA adverse event reports** for both drugs and medical devices into a single, analysis-ready schema — with **built-in pharmacovi

Snowflake2026-06-01 更新00