End-to-end drug safety review integrating FDA labels, FAERS adverse event reports, PRR/ROR disproportionality, pharmacogenomic biomarkers, clinical trial data, and published literature. Use for regulatory drug safety reviews, comprehensive pharmacovigilance reports, label-vs-real-world AE comparison, and clinical decision support for drug safety.
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Low
Low-risk findings worth noting
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tessl review fix ./plugin/skills/tooluniverse-clinical-data-integration/SKILL.mdLow
Low-risk findings.
1 low severity finding. Worth noting, but not necessarily harmful.
The skill exposes the agent to untrusted, user-generated content from public third-party sources, creating a risk of indirect prompt injection. This includes browsing arbitrary URLs, reading social media posts or forum comments, and analyzing content from unknown websites.
Outsider-authored free text is ingested via the user-provided “drug [and event]” parameters that the skill uses to perform database searches at runtime (e.g., DailyMed_show/parse, FAERS counting/disproportionality, ClinicalTrials.gov search, and PubMed search), meaning attacker-controlled text can influence what fetched records are summarized.
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