FDA Drug Adverse Events & Side Effects (openFDA) avatar

FDA Drug Adverse Events & Side Effects (openFDA)

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Pay per usage

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FDA Drug Adverse Events & Side Effects (openFDA)

FDA Drug Adverse Events & Side Effects (openFDA)

Look up reported side effects and adverse events for any drug from the FDA's FAERS database via openFDA. Get the top reported reactions for a drug, or individual adverse-event reports with reactions, seriousness and outcome. No API key needed.

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Pay per usage

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Ken M

Ken M

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3 days ago

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What side effects do people actually report for a drug? This actor answers that from the FDA's own FAERS database (the FDA Adverse Event Reporting System) via the official openFDA API. No API key, no login, no browser.

Two modes

Top reactions (summary) - the best starting point. For each drug, a ranked list of the most reported reactions with how many reports mention each and its share of the drug's reports:

{ "drugs": ["OZEMPIC"], "mode": "reactions", "topReactions": 25 }

Example output: nausea, vomiting, diarrhoea, decreased appetite... each with a report count.

Individual reports - one row per adverse-event report, with:

  • the reactions reported and their outcome (recovered, fatal, ongoing...)
  • seriousness (death, hospitalization, disability, life-threatening)
  • patient sex and age, reporter type (physician, pharmacist, consumer...)
  • country and the other drugs listed in the same report
  • the FDA report ID

Filters

  • seriousOnly - only serious events
  • country - events in one country (US, GB, CA...)
  • sinceYear - only reports from a year onward

Who uses this

  • Pharma, biotech and medical-device companies: pharmacovigilance and competitive safety monitoring - what is being reported about a drug and its competitors.
  • Researchers and universities: study real-world drug safety signals with structured data.
  • Health, legal and insurance analysts: assess reported harm and outcomes for a drug.
  • Journalists and patient advocates: see what the FDA's reporting system actually contains.

Important context

  • Source: FDA FAERS via openFDA (public US government data). Reports are voluntary and unverified - an adverse event report does not mean the drug caused the effect, and counts are influenced by how widely a drug is used and reported. This data supports signal-spotting, not conclusions about causation or safety.
  • The keyless openFDA limit is 1,000 requests/day per IP (shared here). Add your own free openFDA API key to raise it to 120,000/day; it stays private to your run.

Pricing

A small fee per row. Unknown drugs and requests blocked by the daily limit are free note rows, and the first 2 rows of every run are free.