Drug Safety Dashboard

Monitor FDA drug safety data including adverse events from the FAERS database and drug recalls from enforcement reports. Track medication safety trends and alerts in real-time.

Comprehensive Drug Safety Monitoring

Adverse Events: 19M+ reports from FDA's FAERS database (updated July 2025)
Drug Recalls: Class I, II, III recalls and enforcement actions (updated August 2025)
Coverage: Prescription drugs, over-the-counter medications, vaccines, and biologics
Real-time Data: Direct API access to openFDA with no delays

Search FDA's FAERS database (19M+ adverse events) and drug enforcement reports (1,849 Class I recalls)

🚨 Adverse Events Monitor

Recent adverse event reports from FDA's FAERS database (updated July 2025)

No adverse events found

⚠️ Drug Recalls & Safety Alerts

FDA drug enforcement reports and recalls (updated August 2025)

No drug recalls found

Live FDA Data Sources

This dashboard displays real-time data from official FDA surveillance systems:

  • Adverse Events: FDA Adverse Event Reporting System (FAERS) - 19M+ reports
  • Drug Recalls: FDA Drug Enforcement Reports - Class I, II, III recalls and safety alerts
  • Coverage: Prescription drugs, over-the-counter medications, and vaccines

Data refreshed from openFDA API. No API key required for public health data.

Understanding Adverse Events

Death

Most serious outcome requiring immediate attention and investigation

Hospitalization

Events requiring hospital admission or extended hospital stay

Serious Events

Life-threatening events, permanent disability, or birth defects

Non-serious Events

Less severe reactions that don't meet serious criteria

Recall Classifications

Class I Recalls

Dangerous/defective products that could cause serious health problems or death

Class II Recalls

Products that might cause temporary health problems or slight threat of serious injury

Class III Recalls

Products unlikely to cause adverse health reactions but violate FDA regulations

⚠️ Important Safety Information

Medical Disclaimer: This dashboard displays raw FDA data for informational purposes only. Do not use this information to make medical decisions.

Consult Healthcare Providers: Always consult with qualified healthcare professionals regarding medication safety and adverse events.

Data Limitations: Adverse event reports do not prove causation. Multiple factors may contribute to reported events.

Emergency Situations: For medical emergencies, call 911 immediately. Do not rely on this dashboard for urgent medical decisions.

Additional Drug Safety Resources

FDA Safety Communications

  • • Drug Safety Communications
  • • Safety Alerts and Warnings
  • • Medication Guides
  • • Risk Evaluation Programs

Reporting Adverse Events

  • • MedWatch Online Reporting
  • • Healthcare Provider Reporting
  • • Consumer Voluntary Reports
  • • Manufacturer Requirements

Drug Information

  • • Orange Book (Approved Drugs)
  • • Purple Book (Biologics)
  • • Drug Shortages Database
  • • Recalls & Safety Alerts