Fda Database
Access and analyze FDA approval data, clinical trial results, and drug information from Microck's specialized database.
Install on your platform
We auto-selected Claude Code based on this skill’s supported platforms.
Run in terminal (recommended)
claude mcp add microck-fda-database npx -- -y @trustedskills/microck-fda-database
Or manually add to ~/.claude/settings.json
{
"mcpServers": {
"microck-fda-database": {
"command": "npx",
"args": [
"-y",
"@trustedskills/microck-fda-database"
]
}
}
}Requires Claude Code (claude CLI). Run claude --version to verify your install.
About This Skill
What it does
This skill provides access to and querying capabilities for the FDA Adverse Event Reporting System (FAERS) database. It allows users to retrieve information about drugs, adverse events, and patient characteristics reported to the FDA. The data can be used for research, analysis, or monitoring drug safety signals.
When to use it
- Investigating potential side effects of a specific medication.
- Analyzing trends in adverse event reporting for a class of drugs.
- Identifying demographic factors associated with particular adverse events.
- Generating reports on the frequency and severity of reported adverse events.
Key capabilities
- Access to FAERS data
- Querying by drug name
- Querying by adverse event term
- Retrieval of patient characteristics (age, sex, weight)
Example prompts
- "Find all reports of 'headache' associated with the drug 'lisinopril'."
- "What is the most frequently reported adverse event for 'metformin'?"
- "Show me the age distribution of patients reporting 'rash' after taking 'amoxicillin'."
Tips & gotchas
The FAERS database contains voluntarily submitted reports, which may not represent all actual adverse events. Results should be interpreted with caution and validated against other data sources.
Tags
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