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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does FINERENONE Cause Hyponatraemia? 37 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 37 reports of Hyponatraemia have been filed in association with FINERENONE (Kerendia). This represents 1.9% of all adverse event reports for FINERENONE.

37
Reports of Hyponatraemia with FINERENONE
1.9%
of all FINERENONE reports
0
Deaths
12
Hospitalizations

How Dangerous Is Hyponatraemia From FINERENONE?

Of the 37 reports, 12 (32.4%) required hospitalization, and 1 (2.7%) were considered life-threatening.

Is Hyponatraemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for FINERENONE. However, 37 reports have been filed with the FAERS database.

What Other Side Effects Does FINERENONE Cause?

Glomerular filtration rate decreased (250) Hyperkalaemia (209) Blood creatinine increased (181) Death (136) Blood potassium increased (132) Renal impairment (102) Dizziness (77) Acute kidney injury (71) Nausea (63) Urine albumin/creatinine ratio increased (60)

What Other Drugs Cause Hyponatraemia?

FUROSEMIDE (3,127) HYDROCHLOROTHIAZIDE (2,138) OMEPRAZOLE (1,635) LANSOPRAZOLE (1,416) SERTRALINE (1,332) RAMIPRIL (1,178) SPIRONOLACTONE (1,166) PANTOPRAZOLE (1,134) INDAPAMIDE (976) AMLODIPINE (879)

Which FINERENONE Alternatives Have Lower Hyponatraemia Risk?

FINERENONE vs FINGOLIMOD FINERENONE vs FINGOLIMOD LAURYL FINERENONE vs FISH OIL FINERENONE vs FISH OIL\MEDIUM-CHAIN TRIGLYCERIDES\OLIVE OIL\SOYBEAN OIL FINERENONE vs FLAGYL

Related Pages

FINERENONE Full Profile All Hyponatraemia Reports All Drugs Causing Hyponatraemia FINERENONE Demographics