Does FINERENONE Cause Product use issue? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Product use issue have been filed in association with FINERENONE (Kerendia). This represents 0.5% of all adverse event reports for FINERENONE.
10
Reports of Product use issue with FINERENONE
0.5%
of all FINERENONE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product use issue From FINERENONE?
Of the 10 reports, 3 (30.0%) required hospitalization.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FINERENONE. However, 10 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which FINERENONE Alternatives Have Lower Product use issue 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