FDA Drug Adverse Events Reporting System FAERS 2022
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
20
ease of trial
Product Details
Use Cases
Pharmacovigilance monitoring | Regulatory compliance auditing | Drug safety signal detection | Competitive intelligence analysis | Clinical trial risk assessment | Post-market product surveillance | Healthcare provider safety reporting
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
Emerging6 mentions·2 platforms
LinkedIn
5 × 2 pts+10
Blogs & Newsletters
1 × 2 pts+2
Evidence5 sources
LinkedIn
FDA's Use of VAERS for Vaccine Safety Conclusions
Adverse event reporting submitted to FAERS has grown tremendously, but these reports have limitations – importantly, there is no denominator on ...
LinkedIn
FDA Launches Dashboard for Cosmetic Adverse Event Reporting
The FDA announced the launch of the FDA Adverse Event Reporting System (FAERS) Public Dashboard for Cosmetic Products, an interactive tool designed to ...
LinkedIn
FDA launches real-time dashboard for cosmetic safety reports
... adverse event reports in 2022 to over 28,000 in 2023. ... Drug Safety ... The FDA announced the launch of the FDA Adverse Event Reporting System (FAERS) ...
Data Dictionary
Expected fields and columns in this data product
About FDA Drug Adverse Events Reporting System FAERS 2022
FDA Drug Adverse Events Reporting System FAERS 2022 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...