Brand name · Finerenone
Kerendia: adverse event reports filed with FDA
2,062 reports list it as a suspect or interacting product, 2021–2026.
- 2,062
- reports as suspect product
- 0% of all reports · about 420 a year
- 511
- reports, 12 months to June 2026
- 504 in the 12 months before
- 65.4%
- marked serious by the reporter
- 57.4% across all reports
- 7.8%
- record death among outcomes, as reported
- 160 reports · not verified by FDA
2,062 adverse event reports received by FDA list the brand name Kerendia (finerenone) as a suspect or interacting product, from August 2021 to June 2026. A further 397 reports list it only as a concomitant medication, and those are not counted in the figures on this page.
In the 12 months to June 2026, 511 reports listed it, close to the 504 of the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Over its reporting history that is about 420 reports a year and 0% of the 20,646,523 reports in the database. How many people take it is not in the data, so a count is not a rate of occurrence.
The reactions recorded most often are glomerular filtration rate decreased (13%), hyperkalaemia (11.1%) and blood creatinine increased (8%). A report can list several reactions, so shares add to more than 100%; 225 different terms appear across these reports. Glomerular filtration rate decreased is recorded in 13% of these reports, against 0.1% of all reports in the database.
65.4% of the reports are marked serious by the reporter; 7.8% record death among the outcomes and 14.6% record hospitalisation, as reported. 34.7% of the reports came from physicians, and the largest patient age group is 75 and over (20.7%). FDA states that "a causal relationship cannot be established between product and reactions listed in a report" and that for any given report "there is no certainty that a suspected drug caused the event."
Reports by month, five years
Reports by the month FDA received them. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases.
By year received
2026 covers reports received through June 2026 only.
Reactions recorded in the reports
share of Kerendia reports recording the termall reports in the database
- Glomerular filtration rate decreasedreduced kidney filtering13%269
- Hyperkalaemiahigh blood potassium11.1%228
- Blood creatinine increasedraised creatinine, a kidney test8%165
- Blood potassium increased7.3%150
- Deaththe patient died; cause not stated by this term6.6%137
- Renal impairmentreduced kidney function5.5%114
- Dizzinesslight-headedness or unsteadiness4%83
- Acute kidney injurysudden loss of kidney function3.3%68
- Nauseafeeling sick3.1%63
- Hypotensionlow blood pressure2.8%57
- Urine albumin/creatinine ratio increased2.7%56
- Diarrhoealoose or frequent stools2.3%48
- Astheniaweakness or lack of energy2%42
- Fatiguetiredness2%41
- Off label useused for a purpose or in a way not on the label1.8%37
- Vomitingbeing sick1.8%37
- Hyponatraemialow blood sodium1.7%36
- Malaisegeneral feeling of being unwell1.6%34
- Rashskin rash1.6%32
- Dyspnoeashortness of breath1.5%31
- Blood glucose increasedraised blood sugar reading1.4%29
- Headachehead pain1.3%27
- Renal failurekidney failure1.3%27
- Blood pressure increaseda raised blood pressure reading1.1%23
- Product use in unapproved indicationused for a purpose not on the label1.1%23
- Pruritusitching1.1%23
- Dehydrationdehydration1%21
- Blood pressure decreaseda low blood pressure reading0.9%19
- Oedema peripheralswelling of the legs, ankles or hands0.9%19
Top 30 of 225 MedDRA preferred terms recorded across these reports, with a plain-language gloss where one is available. One report can record several terms. The hollow bar is the share of all reports in the database; it describes the reports, not the patients. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic."
Outcomes recorded
Outcome flags as the reporter set them; a report can carry several, and "other serious" is FDA's own category for serious reports outside the named outcomes. Grey bar: all 20,646,523 reports. FDA has not verified any outcome and states that the reports "cannot be used to estimate the incidence of these events."
Patients and reporters
Patient age
Patient sex
Who reported
Age and sex as stated in the report; the reporter's qualification is the primary source recorded by FDA. 71.4% of reports give the United States as the country of the event or reporter.
Reason for use recorded
| Indication as recorded (MedDRA) | Reports | Share |
|---|---|---|
| Chronic kidney disease | 296 | 14.4% |
| Type 2 diabetes mellitus | 155 | 7.5% |
| Diabetic nephropathy | 124 | 6% |
| Cardiac failure | 22 | 1.1% |
| Diabetes mellitus | 21 | 1% |
| Proteinuria | 19 | 0.9% |
The indication field is filled in by the reporter and is often blank; shares are of all 2,062 reports.
In context
| Measure | Kerendia | All reports |
|---|---|---|
| Reports as suspect product | 2,062 | 20,646,523 |
| Share of that pool | — | 0% |
| Reports, latest 12 months | 511 | 1,332,454 |
| Marked serious | 65.4% | 57.4% |
| Death recorded among outcomes, per 1,000 reports | 78 | 91 |
| Hospitalisation recorded, per 1,000 reports | 146 | 213 |
| Consumer-filed share | 27.5% | 45.8% |
| Top term, share of reports | Glomerular filtration rate decreased 13% | 0.1% |
Shares are of reports, not of patients treated. The number of people taking a product is not in the data, so none of these figures is a rate, and differences between columns reflect who takes a product, who reports and how long it has been sold. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic."
Questions about Kerendia reports
How many adverse event reports has FDA received for Kerendia?
2,062 reports list Kerendia as a suspect or interacting product in the openFDA FAERS release of 28 Sep 2026, covering reports received through June 2026. 511 of them arrived in the latest 12 months. Another 397 list it only as a concomitant medication.
What reactions are recorded in Kerendia reports?
glomerular filtration rate decreased (13%), hyperkalaemia (11.1%), blood creatinine increased (8%), blood potassium increased (7.3%) and death (6.6%). These are MedDRA preferred terms coded from what the reporter described; a report can list several, and a term's presence is not a finding that Kerendia was responsible.
How serious are the reports?
65.4% are marked serious by the reporter. Among the outcomes recorded, 7.8% of reports include death and 14.6% include hospitalisation. FDA has not verified these outcomes and states that the reports "cannot be used to estimate the incidence" of the events.
Who files these reports?
physician (34.7%), other health professional (33.3%) and consumer or non-health professional (27.5%). Most reports reach FDA through the manufacturer, which must forward reports it receives.
Are reports for Kerendia rising?
511 reports in the 12 months to June 2026, close to the 504 of the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Counts also move with how many people take a product, its time on the market and publicity.
Do these reports show that Kerendia was responsible for these reactions?
No. FDA states that "a causal relationship cannot be established between product and reactions listed in a report" and that for any given report "there is no certainty that a suspected drug caused the event." The reaction may relate to the condition being treated, to other medicines, or to something else.
Is this a list of the side effects of Kerendia?
No. It is a count of what was reported to FDA. The adverse reactions observed in clinical studies are printed on the FDA-approved label, which a pharmacist or clinician can go through with you.
How do I report an adverse event?
Consumers and health professionals can report to FDA through MedWatch (Form FDA 3500 online, or 1-800-FDA-1088), or to the manufacturer, which must pass reports on. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Drug Adverse Event (FAERS) bulk export released 28 Sep 2026, which holds reports FDA received through 30 Jun 2026. Drug names are as reported, resolved to the brand or generic name on the FDA label where openFDA's harmonisation matched them; classes are the pharmacologic class (EPC) from the label and the National Drug Code Directory of 17 Sep 2026. A report counts here when it lists Kerendia as a suspect or interacting product; reports listing it only as a concomitant medication (397) are excluded. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.