Panadolacetaminophen

According to the FDA label: Uses temporarily relieves minor aches and pains due to: colds flu headache toothache temporarily reduces fever

249,883 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 Panadol 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
Panadol adverse event reports by reporter sex
SexReports
Female136,439
Male82,296
Unknown513

By Age Group

View age group data as a table
Panadol adverse event reports by reporter age group
Age groupReports
0-1713,864
18-3421,294
35-4932,296
50-6444,087
65-7433,398
75+32,547

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 Panadol. 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
Panadol adverse event reports by reported outcome
OutcomeReports
Other Serious134,153
Hospitalization112,729
Death49,469
Non-Serious31,275
Life-Threatening21,378
Disability11,768

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 Panadol. 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
Panadol adverse event reports by year
YearReports
19981
19994
20011
20021
20034
20042,587
20052,680
20063,161
20072,599
20083,858
20092,968
20103,876
20118,089
20128,107
20133,506
20144,189
20156,279
20168,482
20177,660
20189,363
201912,805
202019,916
202120,150
202227,325
202328,089
202428,914
202528,198
2026 (partial)7,071

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 Panadol

In FDA adverse event reports that mention Panadol, 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