Pull serious Ozempic adverse event reports (FAERS)
Brandt May
Returns the 50 FDA FAERS reports most recently received by the FDA that name Ozempic and are flagged serious (for example death, hospitalization or a life-threatening event), from openFDA. Each row lists the drugs on the report, their generic names and manufacturers, the MedDRA reactions and outcomes, and the country where the event occurred. For pharmacovigilance, GLP-1 research and legal teams.
Input
Output fields
Sign up on Apify or log in
The FDA Adverse Events Scraper - FAERS + MAUDE Export Actor is ready to run with the inputs already set for "Pull serious Ozempic adverse event reports (FAERS)". Sign up or log in and you'll land in Apify Console with a copy of this exact task.
Start the "Pull serious Ozempic adverse event reports (FAERS)" task
The FDA Adverse Events Scraper - FAERS + MAUDE Export Actor will start running based on the input automatically. You can also change all the input fields, like choose drug or device reports, product or generic name, and more, to match your specific use case.
Receive the "Pull serious Ozempic adverse event reports (FAERS)" 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 report source, FDA report ID, FDA received date, 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 "Pull serious Ozempic adverse event reports (FAERS)" task via API.

Integrate "Pull serious Ozempic adverse event reports (FAERS)" into your workflow
Connect "Pull serious Ozempic adverse event reports (FAERS)" with 100+ integrations, or run it via API or MCP.
Webhook
n8n
Make
Zapier
Airbyte
Keboola
IFTTT
Hubspot
GDrive
Gmail
Apify MCP
GitHub
Slack
LangChain
LlamaIndex
Flowise
Pinecone
OpenAI
Mastra
Clay