Semaglutide recalls and reported side effects
Pulls the openFDA drug enforcement records naming semaglutide with a 2026 report date — recall number, classification, status, recalling firm, product description, reason, distribution pattern and quantity — and adds the reactions most often reported to FAERS for the same drug as free ranked aggregate rows. Change the drug name for any molecule. $0.30 per 1,000 FDA records.
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Output fields
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The Clinical Trials & FDA API — ClinicalTrials.gov + openFDA Actor is ready to run with the inputs already set for "Semaglutide recalls and reported side effects". Sign up or log in and you'll land in Apify Console with a copy of this exact task.
Start the "Semaglutide recalls and reported side effects" task
The Clinical Trials & FDA API — ClinicalTrials.gov + openFDA Actor will start running based on the input automatically. You can also change all the input fields, like openfda endpoints, drug names, and more, to match your specific use case.
Receive the "Semaglutide recalls and reported side effects" 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 openfda endpoint, recall number, recall class, and more.
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The final output is delivered in JSON, CSV, or Excel format, ready to be plugged into your workflow. You can also run the "Semaglutide recalls and reported side effects" task via API.

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