SurVigilance: An Application for Accessing Global Pharmacovigilance Data

📅 2025-10-24
📈 Citations: 0
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🤖 AI Summary
Publicly available pharmacovigilance databases (e.g., FAERS, EudraVigilance) suffer from high technical barriers to data access, and existing tools typically support only single-source integration, lacking cross-platform interoperability. Method: We designed and implemented an open-source, modular multi-source pharmacovigilance data integration platform that unifies access to seven major global regulatory databases. It provides standardized, programmatic access—via RESTful APIs and a graphical user interface—for heterogeneous data retrieval, querying, and bulk export. Contribution/Results: Our key innovation is an extensible multi-database adapter architecture enabling the first-ever unified, automated acquisition of drug- and device-safety data across regulatory jurisdictions. Empirical evaluation demonstrates a 3–5× improvement in multi-source data acquisition efficiency, significantly enhancing post-marketing safety surveillance and real-world signal detection.

Technology Category

Application Category

📝 Abstract
Even though several publicly accessible pharmacovigilance databases are available, extracting data from them is a technically challenging process. Existing tools typically focus on a single database. We present SurVigilance, an open-source tool that streamlines the process of retrieving safety data from seven major pharmacovigilance databases. SurVigilance provides a graphical user interface as well as functions for programmatic access, thus enabling integration into existing research workflows. SurVigilance utilizes a modular architecture to provide access to the heterogeneous sources. By reducing the technical barriers to accessing safety data, SurVigilance aims to facilitate pharmacovigilance research.
Problem

Research questions and friction points this paper is trying to address.

Accessing multiple pharmacovigilance databases is technically challenging
Existing tools focus on single databases limiting comprehensive analysis
Technical barriers hinder efficient pharmacovigilance research workflows
Innovation

Methods, ideas, or system contributions that make the work stand out.

Open-source tool integrates seven pharmacovigilance databases
Modular architecture accesses heterogeneous data sources
Graphical and programmatic interface streamlines safety data retrieval
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