FDA Drug Adverse Events Reporting System FAERS 2019
The Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) data package contains information on med..
API Access
Est. Price
~$5,000/yr est.
Update Frequency
Annually
Pricing Tiers
1
Regions
1
Quality SignalsB
Freshness
Recently enriched
Complete
75%
API
API Available
Product Overview
Healthcare NLP & Clinical Data Platform$
Offering: A comprehensive suite of NLP-based clinical entity recognition models and structured healthcare datasets for pharmacovigilance, clinical research, and population health analytics.
Best for: Healthcare data scientists and clinical researchers building automated pipelines for medical record de-identification and drug safety monitoring.
Benefits
- Extensive library of pre-trained clinical NLP models
- Multi-language support for clinical de-identification
- High-granularity SDoH and clinical entity extraction
- Cost-effective pricing compared to enterprise-scale healthcare data platforms
Drawbacks
⚠ Limited longitudinal patient journey tracking compared to Komodo Health · ⚠ Requires technical integration via API rather than turnkey dashboard solutionsProduct Intelligence
Value Score
33
quality per $
Coverage
12
geo × freq × depth
Try-ability
15
ease of trial
Product Details
Use Cases
Pharmacovigilance signal detection | Pharmaceutical competitive intelligence | Regulatory compliance monitoring | Clinical safety research | Drug safety risk assessment | Healthcare market trend analysis | Post-marketing surveillance studies
Coverage
United States
Delivery
API
Detected Use Cases
competitive intelligencecompliance regulatoryhealthcare pharmarisk management
Pricing Tiers
Vedex estimate
~$5,000/yr est.
SUBSCRIPTIONMEDIUM
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Get an instant price estimate based on your organization profile — seats, usage rights, and contract term.Estimated ~$5,000/yr est.
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Web Authority
High Authority12 mentions·2 platforms
Academic Papers
8 × 8 pts+64
LinkedIn
4 × 2 pts+8
Evidence5 sources
Academic Papers
Pharmacovigilance Analysis of Drug-Induced ...
by E Liang · 2025 — Data for this study were obtained from the FDA Adverse Event Reporting System (FAERS), a comprehensive pharmacovigilance database that collects voluntary ...
Academic Papers
Crowdsourcing-Based Knowledge Graph Construction for ...
These findings are further validated through comparison with adverse events reported in the FAERS database, providing important patient-centered ...
Academic Papers
Does Attorney Advertising Stimulate Adverse Event ...
by EC Tippett · 2019 · Cited by 2 — The study examined both weekly and monthly volume of reports to FAERS for 28 groups of drugs targeted by attorney advertising, and compared it ...
Data Dictionary
Expected fields and columns in this data product
About FDA Drug Adverse Events Reporting System FAERS 2019
FDA Drug Adverse Events Reporting System FAERS 2019 is an alternative data product offered by John Snow Labs, available on databricks_marketplace. Data is updated annually. API access is available for programmatic integration. Vedex estimates pricing at roughly $5,000/yr (an estimate, not a vendor-published price).
The Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) data package contains information on med..
About John Snow Labs
John Snow Labs is a data provider vendor based in Wilmington, Delaware, USA. The model is a powerful tool for extracting SDoH entities from clinical text. It was specifically trained to identify the conditions in which people are born, grow, live, work, and age that impacts th...