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

Published: 3 February 2025| Version 1 | DOI: 10.17632/mydr3vdzcr.1
Contributor:
Alexander Everhart

Description

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 recreate the figures and tables, users should first run "everhart_et_al_bmj_cohort_construction.do" followed by "everhart_et_al_bmj_analysis.do". Users will need to extract certain zip files and change directory names within the STATA do-files as appropriate. Please see the included read-me file to understand how the code and files are related, as well as the original sources for data. Some files are in ZIP files due to their size.

Files

Institutions

  • Washington University School of Medicine in St. Louis

Categories

Public Health, Medical Device

Licence