Bactrimsulfamethoxazole + trimethoprim

68,099 adverse event reports submitted to the FDA (1997–2026)

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 →
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Top Reported Adverse Events

The most frequently reported events in association with Bactrim 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
Bactrim adverse event reports by reporter sex
SexReports
Male31,492
Female30,541
Unknown114

By Age Group

View age group data as a table
Bactrim adverse event reports by reporter age group
Age groupReports
0-174,797
18-344,519
35-497,919
50-6413,165
65-7410,864
75+7,379

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 Bactrim. 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
Bactrim adverse event reports by reported outcome
OutcomeReports
Hospitalization35,554
Other Serious32,522
Non-Serious10,559
Death8,524
Life-Threatening5,887
Disability2,683

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 Bactrim. 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
Bactrim adverse event reports by year
YearReports
19971
19981
20021
20032
2004794
2005846
2006908
20071,078
20081,367
20091,511
20101,573
20112,063
20122,090
20131,567
20142,023
20153,263
20163,944
20174,059
20185,403
20196,015
20205,693
20215,120
20224,485
20234,438
20244,842
20254,051
2026 (partial)961

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 Bactrim

In FDA adverse event reports that mention Bactrim, 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