Other Titles

  • FDA Adverse Event Reporting Guidance
  • Averse Event Database by FDA 2017
  • FDA Post-Marketing Surveillance Reports 2017
  • FDA Drugs Causing Serious Adverse Effects 2017
  • FDA Reporting System of Adverse Effects 2017


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

FDA Drug Adverse Events Reporting System FAERS 2017 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 2017.

- 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 and 2017

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