FDA MAUDE manufacturer monitor task
Created by
Stas Persiianenko
Monitor FDA MAUDE adverse event reports for one device manufacturer with clean export fields and optional raw JSON.
FDA MAUDE Adverse Event Reports Scraperautomation-lab/fda-maude-adverse-event-reports-scraper
Date received
Event type
Manufacturer
Brand
+8 fieldsTextNumberBooleanListObject
Input
Start date(required):2024-01-01
End date(required):2024-03-31
Manufacturer name:MEDTRONIC PUERTO RICO OPERATIONS CO.
Maximum reports(required):250
Include raw openFDA JSON:true
Output fields
Date received
Event type
Manufacturer
Brand
Device name
Product code
Report number
MDR key
Patient problems
Event description
Source URL
Scraped at
Sign up on Apify01
Create your Apify account to access the FDA MAUDE Adverse Event Reports Scraper.
Start the run02
The Actor will start running based on the input automatically.
Receive the output03
Monitor the progress in real-time. You will be notified as soon as your dataset is complete and ready for review.
Integrate into your workflow04
The final output is delivered in JSON, CSV, or Excel format, ready to be plugged into your workflow.
