PillSignal — FDA Adverse Event Reports

Explore FDA adverse event reports for prescription medications

What is PillSignal?

PillSignal makes FDA adverse event data easy to explore. When people experience unexpected reactions while taking a medication, they — or their doctors — can report it to the FDA through the Adverse Event Reporting System (FAERS). These reports are publicly available, but buried in a database most people have never heard of.

PillSignal surfaces that data in plain language: how many reports exist for a drug, what events were reported, who reported them, and how the numbers have changed over time.

This is real-world data from real patients — different from drug label information, and often more reflective of everyday experience.


What you'll find on each drug page

Reported events

The most frequently reported adverse events for the drug, ranked by how often they appear in FDA reports.

Demographics

Breakdown of who is filing reports — by age group and sex — giving context to the reporting population.

Outcome severity

How serious the reported outcomes were: hospitalization, life-threatening events, disability, and more.

Trends over time

Quarterly report volume going back years, showing whether reporting has increased, decreased, or stayed steady.


About this data: This data reflects voluntary reports submitted to the FDA's Adverse Event Reporting System (FAERS). A report does not mean the medication caused the event. Data may be incomplete or contain errors. Learn more about FAERS.