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openFDA Food Adverse Events Scraper

Pricing

Pay per usage

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openFDA Food Adverse Events Scraper

openFDA Food Adverse Events Scraper

Extract FDA CAERS food adverse event reports from openFDA for product safety monitoring, supplement research, and consumer-health risk analysis.

Pricing

Pay per usage

Rating

0.0

(0)

Developer

Ashwin Prasad

Ashwin Prasad

Maintained by Community

Actor stats

0

Bookmarked

2

Total users

1

Monthly active users

3 days ago

Last modified

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Extract FDA CAERS food adverse event reports from openFDA for food and supplement safety monitoring, consumer-health research, retail compliance, ecommerce product-risk analysis, supplier due diligence, and brand-safety workflows. This actor is useful for retailers, food brands, supplement companies, compliance teams, health researchers, and AI agents that need structured official food adverse-event rows.

What You Can Extract

  • Report number, created date, event start date, outcomes, and reactions
  • Consumer age and gender fields when available
  • Suspect products, all products, industry names, source URL, and raw FDA payload
  • Query metadata for product keywords, reaction terms, and industry filters
  • One row per FDA CAERS adverse-event report returned by openFDA

Common Use Cases

  • Monitor adverse event signals for foods, beverages, dietary supplements, and ingredients
  • Research product safety issues by brand, product keyword, reaction keyword, or industry name
  • Support retail, ecommerce, marketplace, supplier, and private-label compliance workflows
  • Build safety dashboards and risk-review queues for product teams
  • Feed AI agents that summarize recent CAERS reports and flag patterns for human review

SEO Keywords

openFDA food adverse events scraper, FDA CAERS API, food safety data scraper, supplement adverse event reports, consumer health risk data, retail compliance scraper, product safety monitoring, FDA adverse event dataset.

Example Input

{
"productKeyword": "protein",
"reactionKeyword": "nausea",
"industryName": "Dietary Supplements",
"maxResults": 100
}

Output

Rows include report number, created date, event start date, outcome fields, reactions, consumer age and gender fields, suspect products, industry names, source URL, raw FDA payload, and query metadata. Export as JSON, CSV, Excel, or connect to monitoring workflows through the Apify API.

Pricing Recommendation

Launch at $2-$3 per 1,000 adverse-event rows, then increase toward $4-$5 per 1,000 after food-safety, retail-compliance, or supplement-monitoring usage appears. The official openFDA endpoint keeps compute cost low.

Responsible Use

This actor extracts public FDA CAERS reports. Use the data for research, monitoring, and compliance support. Reports do not prove causation; verify important medical, legal, safety, or product decisions with primary FDA records and qualified professionals.