Drug Safety & FDA Brief: Approvals, Adverse Events, Recalls avatar

Drug Safety & FDA Brief: Approvals, Adverse Events, Recalls

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from $17.00 / 1,000 drug briefs

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Drug Safety & FDA Brief: Approvals, Adverse Events, Recalls

Drug Safety & FDA Brief: Approvals, Adverse Events, Recalls

Give it drug names (brand or generic). For each it fuses four openFDA sources - approvals, FAERS adverse events (total, top reactions, serious, deaths), recalls and the boxed warning - into ONE composed safety brief. Keyless, agent-callable. FAERS reports do not establish causation.

Pricing

from $17.00 / 1,000 drug briefs

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Centor Prat

Centor Prat

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Give it drug names (brand or generic) and get ONE composed safety brief per drug — not four separate scrapes. It fuses four openFDA sources into a single answer: approvals (drugsFDA), FAERS adverse events (aggregated), recalls (enforcement) and the boxed warning (label). Keyless, agent-callable, built to answer "what does the FDA safety picture for this drug look like?"

⚠️ Not causation. FAERS adverse-event reports are voluntary and do not establish that a drug caused an event — counts reflect reporting, not incidence or causation. Every brief says so. Verify against the FDA label and source before any clinical or investment decision.

⚡ Why it's different

Every other FDA actor on the Store scrapes one endpoint (events, or approvals, or labels). This one composes all four into one brief per drug, with the adverse events already aggregated server-side (top reactions, serious and death report counts) — the answer, not the raw rows.

📋 What each brief contains

FieldMeaning
approvalSponsors, application numbers, generic/brand names, dosage forms, routes, marketing status
adverseEvents.totalReportsTotal FAERS reports mentioning the drug
adverseEvents.topReactionsMost-reported reactions with counts (aggregated)
adverseEvents.seriousReports / deathReportsReport counts flagged serious / death
recallsTotal recalls + the most recent (reason, classification, status, date, firm)
label.hasBoxedWarningWhether the current label carries a boxed ("black box") warning

📥 Input

{ "drugs": ["semaglutide", "aspirin"] }

One brief per drug. Brand or generic names both work.

📤 Example output (real, trimmed — semaglutide)

{
"drug": "semaglutide", "found": true,
"approval": { "sponsors": ["NOVO"], "dosageForms": ["TABLET"], "marketingStatus": ["Prescription"] },
"adverseEvents": { "totalReports": 7580, "seriousReports": 5734, "deathReports": 232,
"topReactions": [{"reaction":"Nausea","count":1075},{"reaction":"Vomiting","count":940}] },
"recalls": { "total": 1 },
"label": { "hasBoxedWarning": true },
"note": "FAERS reports do not establish that the drug caused the event..."
}

💰 Pricing (pay-per-event)

  • Drug brief — $0.02 per drug for which openFDA returns data. No data = free.

💡 Use cases

  • Pharmacovigilance / pharma: a fast safety snapshot per drug or across a portfolio.
  • Investors / analysts: adverse-event volume, serious/death signal, recalls, boxed warnings at a glance.
  • Health researchers / journalists: a sourced FDA summary per drug.
  • Pair with Clinical Trials Intelligence: pipeline + safety for the same molecule.

🚀 Ready-made tasks (one click)

🤖 For AI agents (MCP)

{ "mcpServers": { "apify": { "url": "https://mcp.apify.com/?tools=actors,docs,centorprat/drug-safety-fda-brief" } } }

Claude Code: claude mcp add --transport http apify "https://mcp.apify.com/?tools=actors,docs,centorprat/drug-safety-fda-brief" --header "Authorization: Bearer <YOUR_APIFY_TOKEN>"

📜 Data & attribution

Source: openFDA (U.S. Food & Drug Administration): drugsFDA, FAERS (drug/event), enforcement/recalls, and labeling. Public data, no login. FAERS reports do not establish causation.