Does FINERENONE Cause Product prescribing issue? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Product prescribing issue have been filed in association with FINERENONE (Kerendia). This represents 1.5% of all adverse event reports for FINERENONE.
28
Reports of Product prescribing issue with FINERENONE
1.5%
of all FINERENONE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Product prescribing issue From FINERENONE?
Of the 28 reports, 4 (14.3%) required hospitalization, and 1 (3.6%) were considered life-threatening.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FINERENONE. However, 28 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 prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)
Which FINERENONE Alternatives Have Lower Product prescribing 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