Pricing

from $100.00 / 1,000 adverse events

FDA Adverse Events — FAERS & MAUDE Records API

Signal-scored adverse-event feed from openFDA FAERS (drugs) + MAUDE (devices). Returns reports with seriousness flags, MedDRA Preferred Terms, and PRR disproportionality signal per drug-event pair. For pharmacovigilance, mass-tort plaintiff intake, device compliance, medical journalism.

Pricing

from $100.00 / 1,000 adverse events

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NexGenData

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19 hours ago

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FDA Adverse Events

FDA adverse-event records from FAERS (drugs) and MAUDE (devices) — for pharmacovigilance signal detection.

Public regulatory/health data — not medical advice.

📊 What you get

Clean JSON, one record per report (full output has 21 fields):

source — Source
report_id — Report id
report_type — Report type
received_date — Received date
occur_country — Occur country
reporter_country — Reporter country
serious — Serious
seriousness_flags — Seriousness flags
patient_age — Patient age
patient_age_unit — Patient age unit

Pricing: $0.100 per report (Pay-Per-Event) — about 10 reports per $1.

🤖 Use with AI agents

Point Claude, the OpenAI Agents SDK, an n8n flow or any MCP-aware client at it and pull official records on demand.

Agentic payments (x402): Supports agentic payment via x402 — agents can call this actor with USDC, no API key required.

FDA & public-health records family:

OpenFDA Drug · Drug Approvals · Drug Shortages · Purple Book · Warning Letters/483 · Pharma Pipeline · Medical Devices

Product-safety recalls: NHTSA Recalls · NHTSA Defects · NHTSA Safety · CPSC Recalls

Agent front door — Healthcare & FDA MCP: Healthcare & FDA MCP

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Healthcare & Medical Data MCP Server

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