Does FINERENONE Cause Wrong technique in product usage process? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Wrong technique in product usage process have been filed in association with FINERENONE (Kerendia). This represents 0.5% of all adverse event reports for FINERENONE.
9
Reports of Wrong technique in product usage process with FINERENONE
0.5%
of all FINERENONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong technique in product usage process From FINERENONE?
Of the 9 reports.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FINERENONE. However, 9 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which FINERENONE Alternatives Have Lower Wrong technique in product usage process 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