Advil Liqui-gelsibuprofen

According to the FDA label: Uses temporarily relieves minor aches and pains due to: headache toothache backache menstrual cramps the common cold muscular aches minor pain of arthritis temporarily reduces fever

198,863 adverse event reports submitted to the FDA (1998–2026)

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 Advil Liqui-gels 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
Advil Liqui-gels adverse event reports by reporter sex
SexReports
Female115,919
Male63,151
Unknown601

By Age Group

View age group data as a table
Advil Liqui-gels adverse event reports by reporter age group
Age groupReports
0-1712,759
18-3421,974
35-4932,347
50-6437,539
65-7418,858
75+12,616

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 Advil Liqui-gels. 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
Advil Liqui-gels adverse event reports by reported outcome
OutcomeReports
Other Serious94,287
Hospitalization69,852
Non-Serious55,275
Death15,997
Life-Threatening12,831
Disability9,006

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 Advil Liqui-gels. 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
Advil Liqui-gels adverse event reports by year
YearReports
19981
20012
20021
20035
20041,610
20052,145
20062,049
20072,278
20081,885
20092,861
20104,874
20116,821
20127,092
20136,756
20146,570
20159,098
201612,495
201711,337
201815,770
201916,898
202015,626
202115,363
202214,934
202313,854
202412,744
202512,790
2026 (partial)3,004

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 Advil Liqui-gels

In FDA adverse event reports that mention Advil Liqui-gels, 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