FDA Insulin Pump Adverse Event Reports
Pull FDA MAUDE reports on insulin pumps for device safety review: mdrReportKey, eventType, deviceNames, patientAgeYears, dateReceived. Serious events only.
FDA Scraper - Recalls, Adverse Events & Device Datascrapesage/fda-scraper
Type
FAERS ID
MAUDE key
Report #
+14 fieldsTextNumberBooleanListObject
Input
What to scrape:deviceAdverseEvents
Keyword:insulin pump
Serious adverse events only:true
Date from:2025-01-01
Output fields
Type
FAERS ID
MAUDE key
Report #
Serious
Seriousness
Event type
Reactions
Outcomes
Suspect drugs
Devices
Suspect products
Sex
Age
Received (drug)
Received (device)
Created (food)
Country
Sign up on Apify01
Create your Apify account to access the FDA Scraper - Recalls, Adverse Events & Device Data.
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.
