FDA Drug Adverse Events Reporting System FAERS 2014
The FDA Adverse Event Reporting System (FAERS) data package contains information on medication errors, quality complai..
API Access
Est. Price
~$1,500/yr est.
Update Frequency
Annually
Pricing Tiers
1
Regions
1
Quality SignalsB
Freshness
Recently enriched
Complete
69%
API
API Available
Product Overview
Healthcare NLP & Clinical Data Platform$
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
37
quality per $
Coverage
12
geo × freq × depth
Try-ability
20
ease of trial
Product Details
Use Cases
Pharmacovigilance signal detection | Pharmaceutical competitive intelligence | Regulatory compliance auditing | Drug safety risk assessment | Clinical trial outcome benchmarking | Post-market surveillance research | Healthcare policy impact analysis
Coverage
United States
Delivery
API
Detected Use Cases
competitive intelligencecompliance regulatoryhealthcare pharmarisk management
Pricing Tiers
Vedex estimate
~$1,500/yr est.
SUBSCRIPTIONMEDIUM
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Get an instant price estimate based on your organization profile — seats, usage rights, and contract term.Estimated ~$1,500/yr est.
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Web Authority
Notable5 mentions·2 platforms
Academic Papers
3 × 8 pts+24
LinkedIn
2 × 2 pts+4
Evidence5 sources
Academic Papers
Detecting adverse high-order drug interactions from ...
This study introduces a computational framework for adverse drug interaction detection, leveraging disproportionality analysis on individual ...
Academic Papers
A Semi-Automated Ontology Building Approach
The Food and Drug Administration (FDA) maintains the FDA Adverse Event Reporting System (FAERS), a database for collecting and sharing adverse ...
Academic Papers
Unpacking the effects of adverse regulatory events
by MJ Higgins · 2018 · Cited by 10 — The. FDA Adverse Events Reporting System (FAERS) database was designed to collect complaints and adverse events for approved drugs. Depending on the ...
Data Dictionary
Expected fields and columns in this data product
About FDA Drug Adverse Events Reporting System FAERS 2014
FDA Drug Adverse Events Reporting System FAERS 2014 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 $1,500/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...