Other Titles

  • FDA Adverse Event Reporting Guidance
  • Averse Event Database by FDA 2018
  • FDA Post-Marketing Surveillance Reports 2018
  • FDA Drugs Causing Serious Adverse Effects 2018
  • FDA Reporting System of Adverse Effects 2018

Keywords

  • Adverse Reaction
  • Adverse Events in Healthcare
  • Adverse Event Reporting Form
  • FAERS
  • Serious Adverse Event
  • Adverse Events Reporting System

FDA Drug Adverse Events Reporting System FAERS 2018 Data Package

The FDA Adverse Event Reporting System (FAERS) data package contains information on medication errors, quality complaints and drug related adverse events that were submitted to FDA in 2018.

Benefits
- Useful for physicians, pharmacists, pharmaceutical companies, medical students and patients (general public). - FAERS database is available on FDA’s website in raw form, whereas a JSL customer gets it in clean and normalized form ready to use and create his own custom reports. - Quarter wise data merged into one file. - Easy to comprehend for the customers who are unfamiliar with the medical terminology as all abbreviated terms are replaced with full form, unlike FAERS original datasets which are full of abbreviations. - Datasets are available for the year 2014, 2015, 2016, 2017 and 2018

Your Data License

Your Data License
  • Research
    Non-Commercial, Share-Alike, Attribution Free Forever
  • Commercial
    Commercial Use, Remix & Adapt, White Label Log in to download
INCLUDED DATASETS