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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.
Clinical Trials & FDA API — ClinicalTrials.gov + openFDAinsight.solutions/clinical-trials-fda-api
openFDA endpoint
Recall number
Recall class
Recall status
+10 fieldsTextNumberBooleanListObject
Input
openFDA endpoints:drug/enforcement+1
Drug names:semaglutide
FDA records dated on or after:2026-01-01
Count fields (free aggregates):patient.reaction.reactionmeddrapt.exact
Maximum FDA records per endpoint:50
Output fields
openFDA endpoint
Recall number
Recall class
Recall status
Recalling firm
Product description
Reason for recall
Record date
Distribution pattern
Quantity
Voluntary or mandated
Firm city
Firm state
Firm country
Sign up on Apify01
Create your Apify account to access the Clinical Trials & FDA API — ClinicalTrials.gov + openFDA.
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.
