Pricing

Pay per event

FDA MAUDE Adverse Event Reports Scraper

Extract FDA MAUDE medical device adverse event reports by date, manufacturer, device, product code, event type, or MDR identifiers.

Pricing

Pay per event

Rating

0.0

(0)

Developer

Stas Persiianenko

Actor stats

Bookmarked

Total users

Monthly active users

7 days ago

Last modified

FDA MAUDE Adverse Event Reports Scraper API

Below, you can find a list of relevant HTTP API endpoints for calling the FDA MAUDE Adverse Event Reports Scraper Actor. For this, you’ll need an Apify account. Replace <YOUR_API_TOKEN> in the URLs with your Apify API token, which you can find under Integrations in Apify Console. For details, see the API reference.

Run Actor

POST
https://api.apify.com/v2/acts/automation-lab~fda-maude-adverse-event-reports-scraper/runs?token=<YOUR_API_TOKEN>

Note: By adding the method=POST query parameter, this API endpoint can be called using a GET request and thus used in third-party webhooks. Please refer to our Run Actor API documentation.

Run Actor synchronously and get dataset items

POST
https://api.apify.com/v2/acts/automation-lab~fda-maude-adverse-event-reports-scraper/run-sync-get-dataset-items?token=<YOUR_API_TOKEN>

Note: This endpoint supports both POST and GET request methods. However, only the POST method allows you to pass input data. For more information, please refer to our Run Actor synchronously and get dataset items API documentation.

Get Actor

GET
https://api.apify.com/v2/acts/automation-lab~fda-maude-adverse-event-reports-scraper?token=<YOUR_API_TOKEN>

For more information, please refer to our Get Actor API documentation.

Actors can be used to scrape web pages, extract data, or automate browser tasks. Use the FDA MAUDE Adverse Event Reports Scraper API programmatically via the Apify API.

You can choose from:

FDA MAUDE Adverse Event Reports Scraper API in Python

FDA MAUDE Adverse Event Reports Scraper API in JavaScript

FDA MAUDE Adverse Event Reports Scraper API through CLI

FDA MAUDE Adverse Event Reports Scraper OpenAPI definition

You can start FDA MAUDE Adverse Event Reports Scraper with the Apify API by sending an HTTP POST request to the Run Actorendpoint. An Actor’s input and its content type can be passed as a payload of the POST request, and additional options can be specified using URL query parameters. The FDA MAUDE Adverse Event Reports Scraper is identified within the API by its ID, which is the creator’s username and the name of the Actor.

When the FDA MAUDE Adverse Event Reports Scraper run finishes you can list the data from its default dataset(storage) via the API or you can preview the data directly on Apify Console.

FDA Medical Device Adverse Event Search (MAUDE)

ryanclinton/fda-device-events

Search the FDA's **MAUDE database of 24 million+ medical device adverse event reports** — including malfunctions, injuries, and deaths. Filter by device name, manufacturer, product code, event type, report number, or date range.

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FDA MAUDE Device Event Monitor

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Monitor medical device adverse events from openFDA MAUDE data.

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openFDA Medical Device Events Scraper

parseforge/openfda-device-event-scraper

Export MAUDE medical-device adverse-event reports from openFDA. Search 24M+ reports by device name, manufacturer, event type, and event-date range. Pull report ID, device, manufacturer, event narrative, patient outcome, and dates.

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US FDA Adverse Events Scraper (FAERS + MAUDE)

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Search FDA adverse-event reports for drugs (FAERS) and medical devices (MAUDE) as clean, flattened records.

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openFDA Medical Device Adverse Events & Recalls Scraper

scrapers_lat/openfda-device-events-scraper

Scrape FDA medical device adverse events (MAUDE), device recalls and 510(k) clearances from the official openFDA API. Extract report number, device brand, manufacturer, event type, product problems and dates across the United States. Export to JSON, CSV or Excel.

Scrapers Lat

5.0

Healthcare Compliance MCP — AI Agent FDA Device Intelligence

red.cars/healthcare-compliance-mcp

Query FDA MAUDE adverse events, 510(k) clearances, and device recalls. One tool call for AI agent medical device compliance research.

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FDA Adverse Events — FAERS & MAUDE Records API

nexgendata/fda-adverse-events-faers-maude

Signal-scored adverse-event feed from openFDA FAERS (drugs) + MAUDE (devices). Returns reports with seriousness flags, MedDRA Preferred Terms, and PRR disproportionality signal per drug-event pair. For pharmacovigilance, mass-tort plaintiff intake, device compliance, medical journalism.

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FDA Food Adverse Events Scraper

crawlerbros/fda-food-adverse-events-scraper

Scrape the FDA CFSAN Adverse Event Reporting System (CAERS) - search 140,000+ food, dietary supplement, and cosmetic adverse event reports by product, reaction type, or date range. No API key required.

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Fda Adverse Event Reporting Extract

jeeves_is_my_copilot/fda-adverse-event-reporting-extract

Public data actor with normalized output.

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FDA MAUDE Intelligence MCP

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Medtech peer benchmarking intelligence for AI agents. Compare device manufacturers safety profiles against product-code peers using FDA MAUDE, 510(k), and enforcement data.

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