• FDA Adverse Event Reporting Guidance
  • Averse Event Database by FDA 2016
  • FDA Post-Marketing Surveillance Reports 2016
  • FDA Drugs Causing Serious Adverse Effects 2016
  • FDA Reporting System of Adverse Effects 2016

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 2016 Data Package

$2,765 $1,929 / YEAR

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 2016

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 and 2017
Specification
Update Frequency: Quarterly
Data Complexity: Complex
Number of Datasets: 7
INCLUDED DATASETS
1. FDA Adverse Events Reporting System Demographics 2016 ($395)
2. FDA Adverse Events Reporting System Drug 2016 ($395)
3. FDA Adverse Events Reporting System Drug Indication 2016 ($395)
4. FDA Adverse Events Reporting System Drug Reaction 2016 ($395)
5. FDA Adverse Events Reporting System Drug Therapy Dates 2016 ($395)
6. FDA Adverse Events Reporting System Patient Outcome 2016 ($395)
7. FDA Adverse Events Reporting System Report Source 2016 ($395)