Welcome to Pharmacovigilance 2.0

Claims Data, integrated in Evidex alongside proprietary clinical trials safety outcomes data and optimized post-approval spontaneous reporting data from the FDA Adverse Event Reporting System (FAERS) and VigiBase, provides pharmacovigilance professionals with the software, data, and anlaytics to track emergining safety issues through multiple data sets, validate signals seen in spontaneous reporting, and engage across these various data sets in a dynamic and proactive manner. 

About Evidex®

Advera Health’s Evidex® is a drug safety data aggregation platform that makes disparate drug safety data actionable though a simple to use yet powerful web-based application, empowering use at all organizational levels. Evidex is the gold standard resource for drug safety knowledge and insight, generated through proprietary curated data and analytics and powerful data integrations, enabling previously unavailable in-depth, rigorous adverse event analysis.

See our Complete Guide to Pharmacovigilance Software


Insight from Licensed RWD

Integrate the data that your oranization already works with. Evidex is built with the flexibility to take in any data set for cross-comparisons. 


Fully Integrated with Evidex

Native integration between Vizient Health System Data and Evidex allows for standardized views, but with the flexibility for deeper customization


Powerful Signal Management

Evidex + Claims = active adverse event detection across multiple datasets.  With MedDRA to ICD-10 mappings, the flexible design allows for customized, pre-defined cohort development for standardized tracking along with the ability to adjust observation protocol based on specific signal evaluation needs.

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