FDA Drug Adverse Events Reporting System FAERS 2023
The Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) data package contains information on med..
API Access
Est. Price
~$5,000/yr est.
Update Frequency
—
Pricing Tiers
1
Regions
—
Quality SignalsC
Freshness
Recently enriched
Complete
56%
API
API Available
Product Overview
Healthcare NLP & Clinical Data Platform$
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
29
quality per $
Try-ability
0
ease of trial
Product Details
Use Cases
Pharmacovigilance monitoring | Regulatory compliance auditing | Clinical trial safety benchmarking | Competitive drug intelligence | Post-market product surveillance | Healthcare risk management | Pharmaceutical market research | Drug safety signal detection
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
Notable7 mentions·2 platforms
Academic Papers
2 × 8 pts+16
LinkedIn
5 × 2 pts+10
Evidence5 sources
Academic Papers
Comprehensive Analysis of Adverse Events Associated ...
by L Li · Cited by 5 — ... FDA Adverse Event Reporting System (FAERS) database.MethodsThis ... FAERS database from the fourth quarter of 2013 to the fourth quarter of 2023.
Academic Papers
A Signal Detection and Analysis Study Based on the Faers ...
by K Lin — Methods: Adverse event data from the FAERS database covering 77 quarters from the first quarter of 2004 to the first quarter of 2023 were ...
LinkedIn
FDA Launches Adverse Event Reporting Tool for Improved ...
... Adverse Event Reporting System (FAERS) look-up tool, designed to improve accessibility and transparency of safety data for drugs and biologics.
Data Dictionary
Expected fields and columns in this data product
About FDA Drug Adverse Events Reporting System FAERS 2023
FDA Drug Adverse Events Reporting System FAERS 2023 is an alternative data product offered by John Snow Labs, available on databricks_marketplace. 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...