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✓ EzBot has access — Search 19.7M+ adverse event reports, 130K+ NDC codes, drug labels, approval histories, and real-time shortage data.
19,684,585 records — Adverse events, medication errors, and product quality issues. Updated weekly from FDA.
Structured product labeling including ingredients, warnings, dosing, and usage instructions for thousands of prescription and OTC drugs.
130,667 records — Complete directory of all drugs manufactured, prepared, or processed by US registered establishments.
Approved brand name and generic drugs, including approval history, therapeutic equivalence, and patent information.
1,848 records — Current and resolved shortages of medically necessary drugs. Updated daily.
Comprehensive data on drug recalls, including reason for recall, hazard classification, and distribution information.
✓ EzBot has access — MAUDE adverse events, 510(k) clearances, PMA approvals, recalls, UDI, and device registration data.
Manufacturer and User Facility Device Experience reports on medical device malfunctions, injuries, and deaths.
Records of medical devices cleared through the Premarket Notification process for substantial equivalence.
Premarket Approval records for Class III high-risk medical devices requiring the most stringent FDA review.
Regulatory classification and requirements for thousands of device types across all medical specialties.
Comprehensive data on medical device recalls, corrections, and removals with hazard classifications.
Unique Device Identifier data from the Global Unique Device Identification Database for device tracking and identification.
✓ EzBot has access — 28,315 enforcement reports + 146,590 CAERS adverse event reports. Updated weekly.
28,315 records — Complete food product recall data including hazard level and distribution info.
146,590 records — Food, dietary supplements, and cosmetics adverse events from CFSAN.
✓ EzBot has access — 500K+ veterinary reports, cosmetics data, tobacco problem reports, and substance registration data.
Adverse event reports for animal drugs and devices.
Adverse events associated with cosmetic products.
Problem reports for tobacco product quality issues.
Complete Response Letters for drug applications.
Chemical substance information from the Global Substance Registration System.
Unique Ingredient Identifiers for substances in drugs, biologics, foods, and devices.
National Subset of Device Definitions for healthcare terminology standardization.
Historically significant documents and data from across the FDA.
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