Binostoalendronate

31,529 adverse event reports submitted to the FDA (2004–2026)

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 Binosto 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
Binosto adverse event reports by reporter sex
SexReports
Female24,655
Male3,494
Unknown73

By Age Group

View age group data as a table
Binosto adverse event reports by reporter age group
Age groupReports
0-1790
18-34199
35-493,909
50-644,725
65-744,270
75+4,178

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 Binosto. 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
Binosto adverse event reports by reported outcome
OutcomeReports
Other Serious20,366
Hospitalization13,797
Disability7,200
Non-Serious5,367
Death4,991
Life-Threatening4,405

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 Binosto. 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
Binosto adverse event reports by year
YearReports
2004716
2005691
2006372
2007412
2008678
2009830
20101,052
20111,549
20123,079
20131,575
20141,029
2015871
2016814
2017880
20181,081
20191,134
20201,567
20212,362
20222,639
20231,969
20242,954
20252,819
2026 (partial)456

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 Binosto

In FDA adverse event reports that mention Binosto, 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