Aspirin

According to the FDA label: Uses temporarily relieves: headache muscle pain toothache menstrual pain pain and fever of colds minor pain of arthritis

500,584 adverse event reports submitted to the FDA (2001–2026)

This data reflects voluntary reports submitted to the FDA's Adverse Event Monitoring System (AEMS), formerly the FDA 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 AEMS. New to this data? Read our guide on how to interpret FDA adverse event reports →
New to FDA adverse event data? Here's how to read these reports →

Top Reported Adverse Events

The most frequently reported events in association with Aspirin in the FAERS database. These are events reported by patients taking this medication, not necessarily caused by it. A single report may include multiple events.

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Ranked by frequency of reports, not severity. The most-reported event is not necessarily the most dangerous or the most common in patients taking this drug.

Who Is Reporting

Demographics of patients in FAERS reports that included this information. Not all reports include patient demographics.

By Sex

View reporter sex data as a table
Aspirin adverse event reports by reporter sex
SexReports
Male239,284
Female229,559
Unknown1,279

By Age Group

View age group data as a table
Aspirin adverse event reports by reporter age group
Age groupReports
0-174,399
18-347,216
35-4923,802
50-6493,811
65-74103,446
75+104,377

This shows who filed reports, reflecting who takes this drug and who tends to report, not who is at greatest risk.

Reported Outcomes

Outcomes recorded in FAERS reports that included Aspirin. A single report may involve multiple reactions, each with a different outcome. These categories are defined by FDA reporting guidelines, not by PillSignal.

View outcome data as a table
Aspirin adverse event reports by reported outcome
OutcomeReports
Other Serious213,097
Hospitalization196,737
Non-Serious141,097
Death45,965
Life-Threatening24,315
Disability15,045

Serious outcomes are far more likely to be reported than mild ones, so this overstates how often outcomes are serious. A recorded death does not mean the drug caused it.

Number of FAERS reports received per quarter for Aspirin. Changes in volume may reflect shifts in prescribing rates, media attention, or reporting behavior, not changes in the medication's safety profile.

View report trend as a table
Aspirin adverse event reports by year
YearReports
20012
20021
20036
20048,881
200511,013
200612,174
20079,984
200811,361
200917,352
201019,426
201122,910
201224,537
201315,904
201428,424
201528,844
201629,279
201728,107
201828,137
201924,818
202020,866
202126,678
202234,732
202330,385
202429,592
202530,501
2026 (partial)6,670

The steep increase around 2004 reflects the FDA's move to electronic submission, not a change in this drug's safety. Trends track reporting volume, not risk.

Medications commonly reported with Aspirin

In FDA adverse event reports that mention Aspirin, these medications appeared most often in the same report.

This reflects co-occurrence in submitted reports, not evidence of drug interaction or combined risk. People often report several medications taken for the same condition or for unrelated reasons. Talk to a doctor or pharmacist about your specific medications.

Other medications with similar adverse event profiles in FDA FAERS reports.

Data Source

This data is sourced from the FDA's Adverse Event Monitoring System (AEMS), formerly FAERS, via the OpenFDA API. PillSignal is not affiliated with the FDA.

View this data on the FDA website →

Data last updated: June 2026