Adverse Event Reporting (Grade A)Security-tested data-ai skill for Claude AI. Grade A. Guide veterinary adverse drug event reporting through FDA CVM and query the openFDA animal adverse event database. Use when a suspected adverse dr

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Reviewed by Daniel Nikulshyn·Updated July 2026

Overview

Guide veterinary adverse drug event reporting through FDA CVM and query the openFDA animal adverse event database. Pharmacovigilance in veterinary medicine follows different pathways than human medicine, with reporting through FDA CVM Form 1932a rather than MedWatch. When a suspected adverse drug reaction occurs in an animal, this skill guides users through the necessary steps for reporting. Users can query existing adverse event data from the openFDA database by drug name, species, or reaction type. They can also gather required information to report a new adverse event, such as the animal's signalment and the product involved. The skill notes the limitations of openFDA adverse event data, including that it represents spontaneous reports, not incidence rates, and that reporting rates are unknown. It also cautions that absence of adverse event reports does not mean a product is safe, and that adverse event reports do not establish causality.

Key features

Queries openFDA animal adverse events endpoint by drug name, species, or reaction type
Aggregates results by reaction type, species, and outcome severity
Guides users through FDA CVM reporting options
Provides required information for reporting, including animal signalment and product details

Pricing

Model: Free
Category: Skills
Rating: No reviews yet

Use cases

Reporting a Suspected Adverse Drug Reaction

Use the tool when an animal experiences a suspected adverse reaction to a drug, vaccine, or pesticide product. Gather required information and guide the user through FDA CVM reporting options.

Checking Reported Adverse Events for a Veterinary Product

Use the tool to search the openFDA animal adverse events endpoint by drug name, species, or reaction type. Aggregate results and present findings with appropriate context.

Pros & Cons

Pros

Facilitates accurate and efficient reporting of veterinary adverse drug events
Provides access to existing adverse event data from the openFDA database
Guides users through FDA CVM reporting options, including online and phone reporting

Cons

openFDA adverse event data represents spontaneous reports, not incidence rates
Reporting rates are unknown, and absence of reports does not mean a product is safe
The openFDA API has rate limits and data may lag behind real-time reporting

Reviews

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Q&A

Are there any limitations to the openFDA data accessed by the tool?

Yes, the data consists of spontaneous reports only, so it does not provide incidence rates, and reporting rates are unknown; the API also has rate limits and may lag behind real‑time reporting.

Asked by Yosef Mizrahi · Sep 12, 2025

What kinds of data can I query from openFDA using this skill?

You can search adverse event reports by drug name, species, or reaction type, then view aggregated results by reaction type, species, and outcome severity.

Asked by Amina Diallo · Aug 23, 2025

How does the tool help with filing a new veterinary adverse drug event report?

It walks users through the steps to complete FDA CVM Form 1932a, gathers essential data such as animal signalment and product details, and offers both online and phone reporting options.

Asked by Diego Fernández · Aug 3, 2025

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