Under maintenance

Pricing

from $20.00 / 1,000 ae-matcheds

Try for free

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FDA Adverse Event Monitor

Under maintenance

Try for free

One event per new FDA adverse event report for the drugs or devices you watch: FAERS reports where your drug is the suspect drug, or MAUDE reports for your device, re-checked for precision. Public openFDA source.

Pricing

from $20.00 / 1,000 ae-matcheds

Rating

0.0

(0)

Developer

Chase Mariano

Actor stats

Bookmarked

Total users

Monthly active users

4 days ago

Last modified

Categories

You can access the FDA Adverse Event Monitor programmatically from your own applications by using the Apify API. You can also choose the language preference from below. To use the Apify API, you’ll need an Apify account and your API token, found in API & Integrations in Apify Console.

Python

JavaScript

CLI

OpenAPI

HTTP

MCP

1from apify_client import ApifyClient
2
3# Initialize the ApifyClient with your Apify API token
4# Replace '<YOUR_API_TOKEN>' with your token.
5client = ApifyClient("<YOUR_API_TOKEN>")
6
7# Prepare the Actor input
8run_input = {}
9
10# Run the Actor and wait for it to finish
11run = client.actor("sovereign_workspace/fda-adverse-event-monitor").call(run_input=run_input)
12
13# Fetch and print Actor results from the run's dataset (if there are any)
14print(f"💾 Check your data here: https://console.apify.com/storage/datasets/{run.default_dataset_id}")
15for item in client.dataset(run.default_dataset_id).iterate_items():
16    print(item)
17
18# 📚 Want to learn more 📖? Go to → https://docs.apify.com/api/client/python/docs/quick-start

FDA Adverse Event Monitor API in Python

The Apify API client for Python is the official library that allows you to use FDA Adverse Event Monitor API in Python, providing convenience functions and automatic retries on errors.

Install the apify-client

$pip install apify-client

Other API clients include:

FDA Adverse Event Monitor API in JavaScript

FDA Adverse Event Monitor API through CLI

FDA Adverse Event Monitor OpenAPI definition

FDA Adverse Event Monitor API

FDA Adverse Event Scraper - FAERS Reports

antishock/fda-adverse-events-faers-scraper

Extract drug adverse event reports from the FDA FAERS database via openFDA. Filter by drug, ingredient, manufacturer, MedDRA reaction, country, seriousness and date. Returns reactions, suspect drugs, patient demographics and outcome flags for pharmacovigilance research.

Ryan Zinburg

Fda Adverse Events Scraper

velvety_bedbug/fda-adverse-events-scraper

Scrape FDA drug adverse event reports (FAERS) and drug labels from the openFDA API. Filter by drug name, reaction, seriousness, and date. No API key required.

Peters Bugs

openFDA Drug Adverse Events Scraper

neuton/openfda-drug-adverse-events-scraper

Search FDA FAERS drug adverse event reports through openFDA by drug name, reaction, country, seriousness, or report date. Export safety report IDs, drugs, reactions, outcomes, dates, and demographics.

Neuton Scripts

OpenFDA Drug Adverse Events Search

scrupulous_waterbird_m4w/openfda-drug-events

Search public FDA FAERS drug adverse-event reports by drug name, raw query, and received-date range. Export normalized safety reports with patient, drug, reaction, and serious-event fields.

Mori

Openfda Drug Events Scraper

velvety_bedbug/openfda-drug-events-scraper

Scrapes FDA drug adverse event reports from the OpenFDA API. Search by drug name, reaction, seriousness, and date range. Access 20M+ adverse event reports. No API key required.

Peters Bugs

FDA Recalls & Adverse Events Monitor (openFDA)

webdatatools/openfda-recall-monitor

FDA Recalls & Adverse Events Monitor returns food, drug and device recalls, drug and device adverse-event reports, and drug labels from openFDA — one flat, scored row per record for a date range you choose.

Murat Uzun

FDA MAUDE — Medical Device Adverse Event & Malfunction Reports

samwise.agency/fda-device-maude

Search FDA MAUDE (Manufacturer and User Facility Device Experience) adverse event reports for medical devices. Report numbers, device names, manufacturer names, event types, dates, patient outcomes, and product problems. Official openFDA data, no API key.

samwise.agency

FDA Intel: Adverse Event Summaries

iceni-data/fda-adverse-event-summaries

Aggregates FDA MAUDE device adverse event reports (openFDA /device/event) into summary rows by product code, manufacturer, or brand -- event-type counts, top device/patient problems, monthly trend, and report-source breakdown. No individual report rows or narratives.

Martyn Gross

FDA Adverse Events Scraper - FAERS + MAUDE Export

maydit/us-fda-adverse-events-scraper

Scrape FDA adverse events from FAERS (drugs) and MAUDE (devices) via openFDA. Deeply nested reports flattened to one clean row each. Export to CSV, JSON, or Excel.