Metformin

294,215 adverse event reports submitted to the FDA (2001–2026)

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 Metformin 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
Metformin adverse event reports by reporter sex
SexReports
Female145,059
Male125,231
Unknown942

By Age Group

View age group data as a table
Metformin adverse event reports by reporter age group
Age groupReports
0-172,599
18-346,699
35-4923,031
50-6471,726
65-7460,036
75+41,177

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 Metformin. 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
Metformin adverse event reports by reported outcome
OutcomeReports
Other Serious125,029
Hospitalization103,659
Non-Serious94,299
Death23,981
Life-Threatening17,688
Disability8,112

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 Metformin. 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
Metformin adverse event reports by year
YearReports
20011
2004294
20051,281
20063,216
2007706
2008751
20091,751
20104,182
20113,169
20125,092
201311,346
201413,906
201524,012
201623,903
201723,222
201826,604
201927,563
202025,797
202121,185
202218,908
202318,837
202417,165
202517,348
2026 (partial)3,976

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 Metformin

In FDA adverse event reports that mention Metformin, 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