Fast OpenFDA Scraper — Drug Recalls & FAERS avatar

Fast OpenFDA Scraper — Drug Recalls & FAERS

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from $0.90 / 1,000 fda adverse event / drug recall extracteds

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Fast OpenFDA Scraper — Drug Recalls & FAERS

Fast OpenFDA Scraper — Drug Recalls & FAERS

Ultra-fast FDA pharmaceutical and drug safety intelligence scraper. Extract FDA drug recalls (Class I, II, III), adverse event safety signals (FAERS), NDC drug approvals, and manufacturer details without browser bloat.

Pricing

from $0.90 / 1,000 fda adverse event / drug recall extracteds

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Developer

Hector

Hector

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2 days ago

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💊 Fast OpenFDA Scraper — Drug Recalls, Adverse Events & Approvals

🎁 Free Tier: Extract up to 1,000 items 100% FREE!

No credit card required • Powered by Apify Free Plan

Every Apify user receives $5.00 in free starter credits every month! You can test and extract up to 1,000 records 100% free with this scraper before paying anything.

Free Trial Monthly Free Credits No Credit Card

👉 Click here to Launch a Free Test Run with 1 Click (Pre-filled)

An enterprise-grade, ultra-fast FDA Pharmaceutical & Drug Safety Scraper powered by the official openFDA regulatory databases. Extract high-ticket Drug Recalls (Class I, II, III), FAERS Adverse Events, and NDC Prescription Approvals with zero browser overhead on 256MB RAM.


🚀 Key Advantages Over Competitors

FeatureLegacy Competitors (scrapers_lat, benthepythondev)Fast OpenFDA Scraper (Ours)
Data ScopeFood recalls only OR limited drug text3-in-1: Drug Recalls, FAERS Events & NDC Approvals
Recall ClassificationFlat textClass I (Fatal/Life-Threatening), Class II & III filtering
Safety Signals (FAERS)UnstructuredStructured MedDRA terms, hospitalization & fatality flags
PerformanceSlow / frequent timeoutsSub-second REST execution on 256MB RAM
ResilienceBreaks on API maintenance100% Guaranteed Non-Empty Output (Verified Baseline)
Proxy OverheadOften requires heavy residential proxiesZero proxy required (openFDA compliant) with optional Apify Proxy

💼 High-Value Use Cases

  • Pharmacovigilance & Safety Monitoring: Track real-time post-market drug reactions and adverse event trends.
  • Pharma Due Diligence & Investment: Hedge funds and biotech analysts monitor FDA enforcement actions and recall velocity.
  • Mass Tort & Legal Research: Class-action legal firms identify Class I drug defects and injury reports.
  • Supply Chain & Generic Drug Clearance: Validate NDC registration status, active pharmaceutical ingredients (API), and manufacturer details.

📥 Input Parameters

ParameterTypeDefaultDescription
modeString"recalls"Choose from: "recalls", "adverse_events", or "ndc_directory".
searchQueryString"Ozempic"Drug brand name, active substance, or recalling firm.
classificationString"all"Filter by hazard class ("Class I", "Class II", "Class III").
seriousnessString"all"Filter adverse events ("all", "serious_only", "fatalities_only").
maxItemsNumber30Maximum number of records to return.

📤 Sample Output (JSON)

{
"recordType": "drug_recall",
"identifier": "D-1178-2024",
"title": "Metformin Hydrochloride Extended-Release Tablets, USP 500 mg",
"firm": "Marksans Pharma Limited / Time-Cap Labs, Inc.",
"classification": "Class I",
"status": "Ongoing",
"details": {
"reasonForRecall": "Presence of N-Nitrosodimethylamine (NDMA) impurity detected above acceptable limits.",
"productDescription": "Metformin Hydrochloride Extended-Release Tablets, USP 500 mg.",
"distributionPattern": "Nationwide in the USA to wholesalers and distributors.",
"reportDate": "2024-06-12",
"voluntaryMandated": "Voluntary Firm Initiated"
},
"fdaUrl": "https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts"
}

🛡️ Integration & Automation

Compatible with Zapier, Make.com, n8n, Airtable, and Google Sheets via Apify Webhooks and REST API.