FDA Adverse Drug Event Report Monitor
Logiover
Monitor adverse drug event reports from the FDA. Receive up to 200 records of valuable safety data for effective analysis.
Input
Output fields
Sign up on Apify or log in
The FDA Data Scraper - openFDA Recalls & Events Actor is ready to run with the inputs already set for "FDA Adverse Drug Event Report Monitor". Sign up or log in and you'll land in Apify Console with a copy of this exact task.
Start the "FDA Adverse Drug Event Report Monitor" task
The FDA Data Scraper - openFDA Recalls & Events Actor will start running based on the input automatically. You can also change all the input fields, like dataset and max records, to match your specific use case.
Receive the "FDA Adverse Drug Event Report Monitor" 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 dataset, product recall number, recalling firm, 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 Adverse Drug Event Report Monitor" task via API.
