Farxigadapagliflozin
According to the FDA label: FARXIGA (dapagliflozin) is indicated: • To reduce the risk of sustained eGFR decline, end-stage kidney disease, cardiovascular death, and hospitalization for heart failure in adults with chronic kidney disease at risk of progression. • To reduce the risk of cardiovascular death, hospitalization for heart failure, and urgent heart failure visit in adults with heart failure.
53,579 adverse event reports submitted to the FDA (2008–2026)
Top Reported Adverse Events
The most frequently reported events in association with Farxiga 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.
Show these terms with plain-language definitions
Tap any term below for a plain-language definition.
Death 7,496 reports
A report that the person died. A death appearing in reports for a drug does not mean the drug caused it. Reports record that a death occurred while the medication was being used, which can happen for many unrelated reasons.
Full definition in the glossary →Fatigue 2,383 reports
Extreme tiredness or lack of energy that does not improve with rest.
Full definition in the glossary → See all drugs reporting this event →Nausea 2,344 reports
The feeling of sickness in your stomach that often comes before vomiting.
Full definition in the glossary → See all drugs reporting this event →Dizziness 2,206 reports
A feeling of being lightheaded, unsteady, or like the room is spinning.
Full definition in the glossary → See all drugs reporting this event →Diarrhoea 2,191 reports
Loose or watery bowel movements, often frequent. Also spelled diarrhea in American English.
Full definition in the glossary → See all drugs reporting this event →Dyspnoea 2,066 reports
Shortness of breath or difficulty breathing. Also spelled dyspnea in American English.
Full definition in the glossary → See all drugs reporting this event →Weight Decreased 1,903 reports
Blood Glucose Increased 1,902 reports
A blood test result showing a higher than normal blood sugar level.
Full definition in the glossary →Off Label Use 1,862 reports
Using a medication for a condition or in a way that the FDA has not officially approved. This is common and often legal, and a report of it does not mean something went wrong. Doctors sometimes prescribe drugs off label based on their judgment.
Full definition in the glossary →Acute Kidney Injury 1,787 reports
A sudden drop in how well the kidneys are working. It is often temporary and can have many causes.
Full definition in the glossary →Vomiting 1,727 reports
Throwing up the contents of the stomach.
Full definition in the glossary → See all drugs reporting this event →Headache 1,572 reports
Pain in the head or upper neck.
Full definition in the glossary → See all drugs reporting this event →Diabetic Ketoacidosis 1,543 reports
A serious complication of diabetes where the blood becomes too acidic, needing urgent medical care.
Full definition in the glossary →Pain 1,422 reports
A general report of physical discomfort, used when no more specific location is given.
Full definition in the glossary →Malaise 1,415 reports
A general feeling of being unwell or uncomfortable, without a specific symptom.
Full definition in the glossary →
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
| Sex | Reports |
|---|---|
| Male | 25,733 |
| Female | 21,555 |
| Unknown | 54 |
By Age Group
View age group data as a table
| Age group | Reports |
|---|---|
| 0-17 | 298 |
| 18-34 | 745 |
| 35-49 | 2,563 |
| 50-64 | 8,314 |
| 65-74 | 7,261 |
| 75+ | 7,672 |
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 Farxiga. 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
| Outcome | Reports |
|---|---|
| Other Serious | 25,773 |
| Hospitalization | 15,185 |
| Non-Serious | 12,828 |
| Death | 9,181 |
| Life-Threatening | 3,052 |
| Disability | 1,241 |
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.
Report Volume Over Time
Number of FAERS reports received per quarter for Farxiga. 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
| Year | Reports |
|---|---|
| 2008 | 1 |
| 2009 | 10 |
| 2010 | 9 |
| 2011 | 7 |
| 2012 | 11 |
| 2013 | 9 |
| 2014 | 860 |
| 2015 | 1,530 |
| 2016 | 1,254 |
| 2017 | 1,288 |
| 2018 | 1,574 |
| 2019 | 1,467 |
| 2020 | 1,725 |
| 2021 | 2,889 |
| 2022 | 5,130 |
| 2023 | 8,705 |
| 2024 | 11,377 |
| 2025 | 12,877 |
| 2026 (partial) | 2,856 |
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 Farxiga
In FDA adverse event reports that mention Farxiga, these medications appeared most often in the same report.
- Metformin (10,391 reports)
- Furosemide (5,537 reports)
- Aspirin (5,262 reports)
- Bisoprolol (4,818 reports)
- Spironolactone (4,123 reports)
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.
Related Drugs
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