tooluniverse-pharmacovigilance - Analyze drug safety signals and pharmacogenomic risks
Analyzes drug safety using FDA adverse event reports, labeling, pharmacogenomic data, clinical trials, pathways, and literature, including PRR and ROR signals.
Tags
Updated: 2026-10-16Capabilities
Typical Inputs
Typical Outputs
What this skill does
- Resolve standardized drug identifiers
- Query adverse event reports
- Calculate PRR and ROR
- Stratify serious adverse events
- Extract label safety warnings
- Assess pharmacogenomic risk variants
- Summarize clinical trial safety
- Analyze safety-related pathways
- Review safety literature
- Prioritize actionable safety signals
- Synthesize risk-benefit findings
Inputs
- Drug name or safety question
- FAERS adverse event data
- FDA drug labeling data
- PharmGKB annotations
- Clinical trial safety data
- Pathway data
- Published safety literature
Outputs
- Markdown safety report
- Ranked adverse event CSV
- Pharmacogenomic risk CSV
- Label safety summary
- Clinical trial safety summary
- Prioritized signal list
- Risk-benefit assessment
Requirements
- ToolUniverse data-source access
- File creation and write permission
- Access to FAERS tools
- Access to DailyMed tools
- Access to PharmGKB tools
- Access to clinical trial tools
- Access to pathway and literature tools