pipeworx-fdaUS FDA open data — adverse drug event reports, drug labeling/package inserts, and food recall enforcement actions
Install via ClawdBot CLI:
clawdbot install b-gutman/pipeworx-fdaGrade Fair — based on market validation, documentation quality, package completeness, maintenance status, and authenticity signals.
Sends data to undocumented external endpoint (potential exfiltration)
POST → https://gateway.pipeworx.io/fda/mcpCalls external URL not in known-safe list
https://pipeworx.io/packs/fdaAI Analysis
The skill's external API calls are consistent with its stated purpose of accessing FDA open data, and no hidden instructions or credential harvesting patterns are present. However, the endpoint is not in a known-safe list and data transmission occurs to a third-party service (pipeworx.io), creating a low-risk privacy consideration.
Audited Apr 16, 2026 · audit v1.0
Generated May 20, 2026
Pharmaceutical companies and regulatory bodies can use the tool to search adverse drug event reports for a specific medication, enabling early detection of safety signals and informed risk-benefit assessments.
Healthcare providers can quickly retrieve official prescribing information, including contraindications and dosage guidelines, to inform treatment decisions and reduce medication errors.
Retailers and food distributors can monitor enforcement actions to identify recalled products, remove them from shelves promptly, and maintain regulatory compliance.
Research analysts can analyze FAERS data to identify adverse event patterns for competitor drugs, uncovering potential market opportunities or risks for their own pipeline.
Patient advocacy groups can search drug labels and adverse events to provide evidence-based information to patients about medication risks and proper use.
Offer a limited number of free API calls per month for basic searches, then charge for higher volume, advanced analytics, or real-time alerts on recalls and adverse events.
License the tool as an integrated module within electronic health records (EHR) or clinical decision support systems, providing contextual drug safety information to clinicians.
Use the FDA data to generate custom reports and trend analyses for pharmaceutical companies, helping them monitor post-market safety or conduct due diligence for acquisitions.
💬 Integration Tip
No API key is required; simply use the provided MCP config with npx to set up the server. Start with a simple curl command to test the endpoint before integrating into your application.
Scored May 20, 2026
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