Multiple categories of patient-reported adverse event reports and medication errors including drug names and side effects. These records facilitate post-market safety monitoring of pharmaceutical performance based on real-world incidents submitted to the FDA.
Use Cases
- Identify potential safety signals by analyzing the frequency of specific side effects for a given drug name
- Monitor post-market drug performance by tracking the volume of adverse reactions over time
- Support pharmacovigilance efforts by identifying common patterns in patient-reported drug side effects
Strengths
- Includes drug names associated with each reported adverse event
- Contains descriptions of patient-reported side effects and reactions
- Categorizes incidents based on the nature of the adverse drug experience