Can this skill help with pharmacovigilance?

Yes, it provides access to the Adverse Event Reporting System (FAERS), allowing for safety signal detection and reaction frequency analysis.

Do I need an API key to use the FDA Database skill?

While not strictly required for low-volume queries, a free API key from openFDA is recommended to increase rate limits from 1,000 to 120,000 requests per day.

Does the skill support data visualization?

While the skill focuses on data retrieval and analysis, the returned structured data can be easily processed by Claude to generate reports, tables, or trend summaries.

What types of products can I research with this skill?

You can research human drugs, medical devices, food products, dietary supplements, animal/veterinary drugs, and chemical substances.

FDA Regulatory Database Access

Name: FDA Regulatory Database Access
Author: Microck

byMicrock

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数据科学与机器学习

Accesses and analyzes comprehensive FDA regulatory data for drugs, medical devices, food safety, and substances through the openFDA API.

关于

This skill enables Claude to query the openFDA initiative's vast public datasets, providing real-time access to information on pharmaceuticals, medical devices, and food safety. It streamlines the process of monitoring adverse events, tracking product recalls, identifying substances via UNII or CAS numbers, and researching regulatory submissions like 510(k) clearances or PMA approvals. Ideal for researchers, regulatory affairs professionals, and healthcare developers, it provides standardized Python interfaces to perform complex pharmacovigilance, safety signal detection, and market surveillance directly within the coding workflow.

主要功能

Monitor product recalls and enforcement actions across FDA categories
Analyze temporal trends and safety profiles for comparative research
Research regulatory submissions, including 510(k) and PMA approvals
81 GitHub stars
Query adverse event reports for drugs, devices, and food products
Perform substance identification using UNII, CAS numbers, and names

使用场景

Post-market surveillance and pharmacovigilance for drug safety signal detection
Tracking food allergen recalls and dietary supplement adverse events
Competitive analysis of medical device clearances and classifications

关于

主要功能

Monitor product recalls and enforcement actions across FDA categories
Analyze temporal trends and safety profiles for comparative research
Research regulatory submissions, including 510(k) and PMA approvals
81 GitHub stars
Query adverse event reports for drugs, devices, and food products
Perform substance identification using UNII, CAS numbers, and names

使用场景

Post-market surveillance and pharmacovigilance for drug safety signal detection
Tracking food allergen recalls and dietary supplement adverse events
Competitive analysis of medical device clearances and classifications