FDA Drug Adverse Events Reporting System FAERS 2018
The FDA Adverse Event Reporting System (FAERS) data package contains information on medication errors, quality complai..
API Access
Est. Price
~$5,000/yr est.
Update Frequency
Annually
Pricing Tiers
1
Regions
1
Quality SignalsB
Freshness
Recently enriched
Complete
69%
API
API Available
Product Overview
Healthcare NLP & Clinical Data Platform$
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
33
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 monitoring | Clinical trial safety benchmarking | Investment risk assessment | Drug safety research | Healthcare policy analysis
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
Emerging5 mentions·1 platform
LinkedIn
5 × 2 pts+10
Evidence5 sources
LinkedIn
FDA Adverse Event Reports in One Dashboard
With the new system, adverse event reports submitted to the FDA for drugs, biologics, vaccines, cosmetics, and animal food can be displayed ...
LinkedIn
FDA updates safety labeling guidance for drugs and biologics
The guidance now includes reduced effectiveness as a safety concern, meaning labeling must reflect not just adverse events but also diminished therapeutic ...
LinkedIn
EMMA International's Post
... FDA Adverse Event Reporting System (FAERS) is the most effective method. ... adverse events, and reports related to medication errors (FDA, 2018).
Data Dictionary
Expected fields and columns in this data product
About FDA Drug Adverse Events Reporting System FAERS 2018
FDA Drug Adverse Events Reporting System FAERS 2018 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 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...