Preparing your experience...
Preparing your experience...
Run complete pharmacovigilance workflows and download professional reports
Each dashboard guides you through a standard PV workflow step by step, calling live databases through AlgoVigilance Station. At the end of each workflow, download a structured report ready for review, filing, or sharing.
1. Choose a Workflow
Pick the PV process you need to run
2. Follow the Steps
Each step queries live databases with real data
3. Download Your Report
Professional PDF with all findings and citations
Submit an adverse event report with automated regulatory triage. Validates ICSR completeness, classifies seriousness, determines expedited reporting, and calculates submission deadlines.
Complete safety profile for any drug. Resolves identity, pulls FAERS data, computes signals, reviews labeling, and searches literature.
Investigate a specific drug-event pair. Runs disproportionality analysis, checks label status, finds published evidence, and renders a signal verdict.
Determine whether a drug caused an adverse event using standardized algorithms. Interactive Naranjo scoring and WHO-UMC categorization.
Weigh drug benefits against safety risks using quantitative frameworks. Pulls trial data, FAERS outcomes, and labeling to compute QBRI scores.
Navigate the regulatory landscape for any drug. Search ICH guidelines, FDA approval history, and EMA safety communications.
Compare safety profiles across drugs in the same class. Head-to-head disproportionality, clinical trial activity, and pipeline analysis.
Powered by AlgoVigilance Station — 2,023 pharmacovigilance tools at mcp.nexvigilant.com. Every query hits live FDA, NIH, and NLM databases in real time.