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Fda Adverse Events

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Public data actor with normalized output.

Pricing

Pay per usage

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Developer

Alexander Abernathy

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3 days ago

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FDA MAUDE Adverse Events

Ideal for medical device researchers, patient safety advocates, legal teams, and compliance professionals who need to monitor FDA MAUDE adverse event data at scale. This actor queries the OpenFDA MAUDE API to return structured adverse event records for any device type or manufacturer.

Who uses this: Medical device manufacturers tracking post-market safety, law firms researching device liability, health researchers studying adverse event patterns.

Limitations: Data reflects reports submitted to FDA MAUDE; not all adverse events are reported. PII is redacted in MAUDE records. Search results depend on OpenFDA rate limits (~15 requests/minute per IP).

Fetch medical device adverse event reports from FDA MAUDE database.

Best for

Retrieves adverse event and product problem reports from the MAUDE (Manufacturer and User Facility Device Experience) database.

Input

Field	Type	Required	Default	Description
`queries`	string[]	Yes	-	Medical device or event queries
`maxItemsPerQuery`	integer	No	100	Max records per query (1-1000)
`includeRaw`	boolean	No	false	Include raw payload in output

Example Queries

"pacemaker" - Medical device
"infusion pump" - Device type
"adverse event" - Event type

Output

Field	Type	Description
`source`	string	Always "openfda_maude"
`query`	string	Original search query
`recordType`	string	"adverse_event" or "error"
`title`	string	Medical device name
`identifier`	string	FDA report number
`date`	string	Report received date
`url`	string	Link to FDA MAUDE database
`summary`	string	Event description, outcome

Example input

{
  "queries": ["pacemaker", "infusion pump"],
  "maxItemsPerQuery": 50,
  "includeRaw": false
}

Example output

[
  {
    "source": "openfda_maude",
    "query": "pacemaker",
    "recordType": "adverse_event",
    "title": "Cardiac Pacemaker",
    "identifier": "FDA-MAUDE-2024-001234",
    "date": "2024-02-15",
    "url": "https://www.fda.gov/medical-devices/medical-device-safety/maude-database",
    "summary": "Device malfunction reported | Patient injury: Minor | Outcome: Recovered"
  }
]

Notes

Data sourced from OpenFDA MAUDE API
Adverse event reports are confidential
Check FDA MAUDE for official information

Pricing

This actor uses the Apify Pay-Per-Event model at $0.002 per dataset item.

Example cost: 1,000 items ≈ $2 in actor charges (plus standard Apify platform compute).

Version: 0.1.0
Author: OpenClaw/Apify

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