FDA Drug Adverse Events Reporting System FAERS 2016
The FDA Adverse Event Reporting System (FAERS) data package contains information on medication errors, quality complai..
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 signal detection | Clinical safety research | Regulatory compliance monitoring | Pharmaceutical market intelligence | Drug safety trend analysis | Post-marketing surveillance | Competitive product benchmarking
Delivery
API
Detected Use Cases
competitive intelligencecompliance regulatoryhealthcare pharma
Pricing Tiers
Vedex estimate
~$5,000/yr est.
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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
Emerging4 mentions·2 platforms
Academic Papers
1 × 8 pts+8
LinkedIn
3 × 2 pts+6
Evidence4 sources
Academic Papers
Bisphosphonates and Cardiac Arrhythmia: An Analysis of ...
by F Wang — Methods: From January 2016 to June 2022, reports for BP-related cardiac arrhythmia adverse event from the FDA Adverse Event Reporting System ( ...
LinkedIn
FDA starts daily publication of adverse event data
The FDA's move to publish daily FAERS adverse event data is an innovative step forward for pharmacovigilance, offering substantial benefits in transparency.
LinkedIn
FDA to publish adverse event data daily
#FDA announced it will begin publishing adverse event reports from FAERS daily, rather than quarterly. That's a major shift in the agency's ...
Data Dictionary
Expected fields and columns in this data product
About FDA Drug Adverse Events Reporting System FAERS 2016
FDA Drug Adverse Events Reporting System FAERS 2016 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 FDA Adverse Event Reporting System (FAERS) data package contains information on medication errors, quality complai..
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...