Bisoprolol

132,273 adverse event reports submitted to the FDA (2003–2026)

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 Bisoprolol 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
Bisoprolol adverse event reports by reporter sex
SexReports
Male62,473
Female58,270
Unknown188

By Age Group

View age group data as a table
Bisoprolol adverse event reports by reporter age group
Age groupReports
0-171,002
18-341,955
35-496,156
50-6423,657
65-7431,274
75+43,607

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 Bisoprolol. 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
Bisoprolol adverse event reports by reported outcome
OutcomeReports
Other Serious75,455
Hospitalization73,473
Death14,616
Life-Threatening13,439
Disability6,249
Non-Serious4,286

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 Bisoprolol. 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
Bisoprolol adverse event reports by year
YearReports
20031
2004517
2005587
2006665
2007737
20081,099
20091,394
20101,735
20112,603
20123,635
20133,373
20143,981
20155,368
20166,427
20176,757
201810,787
201911,579
202012,132
202111,240
202212,251
202311,395
202411,199
202510,445
2026 (partial)2,366

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 Bisoprolol

In FDA adverse event reports that mention Bisoprolol, 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