Pricing

$3.00 / 1,000 results

openFDA Drug Adverse Events Scraper

Search FDA FAERS drug adverse event reports through openFDA by drug name, reaction, country, seriousness, or report date. Export safety report IDs, drugs, reactions, outcomes, dates, and demographics.

Pricing

$3.00 / 1,000 results

Rating

0.0

(0)

Developer

Ashwin Prasad

Actor stats

Bookmarked

Total users

Monthly active users

a day ago

Last modified

Why this actor

Drug adverse-event data is valuable to pharmacovigilance teams, health-tech companies, researchers, consultants, investors, and regulatory intelligence workflows. This actor uses the public openFDA FAERS endpoint and supports optional openFDA API keys for heavier production runs, making it suitable for both exploratory safety checks and scheduled monitoring.

SEO keywords covered by this Store page include openFDA adverse events scraper, FAERS drug safety data, FDA adverse event reports API, pharmacovigilance scraper, drug reaction dataset, medication safety monitoring, and regulatory intelligence data.

Output

Safety report ID, received date, country, seriousness flag
Patient age and sex when published
Medicinal products, reactions, and outcomes
Primary-source qualification and raw official FAERS record

Use cases

Monitor public adverse-event reports for watched drugs or active ingredients.
Build pharmacovigilance, market-safety, or regulatory research workflows.
Compare reactions, outcomes, seriousness, country, and report dates across searches.
Feed AI agents with source-linked FAERS rows for safety summaries.
Enrich internal dashboards with official public adverse-event records.

Example input

{
  "drugNames": [
    "aspirin"
  ],
  "maxResultsPerSearch": 5
}

Agent and automation workflows

Schedule this actor for monitored products, push rows to a warehouse or Airtable, and let agents summarize new reactions, seriousness patterns, geographic changes, or emerging safety themes. It pairs well with openFDA drug recalls, drug labels, NDC directory, and drug shortage actors.

Responsible use

This actor extracts public FDA/openFDA data for research and monitoring. FAERS reports are not proof of causation and may be incomplete, duplicated, or unverified. Do not use the output as medical advice; verify clinical, regulatory, or safety decisions against authoritative FDA materials and expert review.

Pricing

Launch around $3 per 1,000 adverse-event rows. Keep a small free allowance for testing, then raise pricing if recurring pharmacovigilance or regulated-data usage appears.

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