How current is the FDA safety data provided by OpenFDA?

FDA data is typically updated quarterly with a 3-6 month reporting lag. However, medical device events and recalls may appear more quickly after publication.

Can I search for drug adverse events using a generic drug name?

Yes. The `drug_name` parameter for searching drug adverse events (FAERS) is designed to search both brand and generic drug names, leveraging OpenFDA's comprehensive drug terminology.

Do I need an FDA API key to use OpenFDA?

No. The OpenFDA API is free and open, and the OpenFDA server automatically handles rate limiting (240 requests/min), so you do not need your own API key.

Does OpenFDA support advanced filtering and custom query syntax?

Yes. Each tool within OpenFDA includes a `search` parameter that accepts raw OpenFDA query syntax, allowing advanced users to implement highly specific and custom data filtering.

OpenFDA

Name: OpenFDA
Author: Taru0208

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Provides AI agents with direct access to comprehensive FDA safety data, including drug adverse events, recalls, and medical device incidents.

The OpenFDA tool serves as an MCP (Model Context Protocol) server, enabling AI agents and compatible clients like Claude Desktop or Cursor to tap into vast FDA safety datasets. It offers direct search capabilities across over 20 million drug adverse event reports (FAERS), 23 million medical device incidents (MAUDE), and tens of thousands of drug and food recall enforcement reports. Built on the Apify platform, it streamlines access to critical public health information, handling API interactions and rate limiting, making it a powerful resource for safety analysis and monitoring without requiring an OpenFDA API key.

主な機能

01Supports custom OpenFDA query syntax for advanced filtering

020 GitHub stars

03Automatic handling of OpenFDA API rate limiting

04Search medical device adverse event reports (MAUDE)

05Search drug adverse event reports (FAERS) by drug name, date, severity

06Search FDA drug and food recall enforcement reports

ユースケース

01Monitor recent Class I drug recalls or food recalls involving specific contaminants.

02Analyze common adverse reactions reported for specific medications like Ozempic.

03Investigate adverse events and incidents related to medical devices such as insulin pumps.