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.
Input
Output fields
Sign up on Apify or log in
The FDA Scraper - Recalls, Adverse Events & Device Data Actor is ready to run with the inputs already set for "FDA Insulin Pump Adverse Event Reports". Sign up or log in and you'll land in Apify Console with a copy of this exact task.
Start the "FDA Insulin Pump Adverse Event Reports" task
The FDA Scraper - Recalls, Adverse Events & Device Data Actor will start running based on the input automatically. You can also change all the input fields, like what to scrape, keyword, and more, to match your specific use case.
Receive the "FDA Insulin Pump Adverse Event Reports" output
Monitor the progress in real time. You will be notified as soon as your dataset is complete and ready for review. Each result includes data such as type, FAERS ID, MAUDE key, and more.
Integrate into your workflow
The final output is delivered in JSON, CSV, or Excel format, ready to be plugged into your workflow. You can also run the "FDA Insulin Pump Adverse Event Reports" task via API.
