finerenone

Brand: Kerendia

Prototype: spironolactone
Drug Class: mineralocorticoid receptor antagonist
Drug Family: diuretic
Subclass: non-steroidal selective MRA
Organ Systems: cardiovascularrenal

Mechanism of Action

Non-steroidal MRA with high aldosterone receptor selectivity; larger volume of distribution; reduces inflammation and fibrosis in kidneys and heart.

mineralocorticoid receptor

Indications

  • CKD with type 2 diabetes (FIDELIO-DKD, FIGARO-DKD)
  • HFrEF (FINEARTS-HF, emerging)

Contraindications

  • hyperkalemia
  • severe renal impairment
  • Addison's disease
  • strong CYP3A4 inhibitors
  • grapefruit

Adverse Effects

Common

  • hyperkalemia
  • hypotension
  • hyponatremia

Serious

  • serious hyperkalemia

Pharmacokinetics (ADME)

Absorption ~43% oral bioavailability; reduced by grapefruit
Distribution large Vd
Metabolism CYP3A4 (major), CYP2C8 (minor)
Excretion renal 80%, fecal 20%
Half-life 2-3 hours
Onset 0.5-1.25 hours
Peak ~1.5 hours
Duration 24 hours
Protein Binding 92%
Vd 52.6 L

Drug Interactions

Drug / Agent Mechanism Severity
strong CYP3A4 inhibitors increased finerenone levels — contraindicated major
ACE inhibitors/ARBs additive hyperkalemia major
grapefruit juice increases finerenone AUC — avoid moderate

Nursing Considerations

  1. FIDELIO-DKD: reduced progression to ESRD in T2DM+CKD
  2. Monitor K+ at initiation and 1 month, then periodically
  3. Avoid grapefruit; avoid strong CYP3A4 inhibitors
  4. Non-steroidal: no hormonal side effects

Clinical Pearls

  • First non-steroidal MRA approved for diabetic CKD
  • FIDELIO-DKD + FIGARO-DKD: reduced CV events and CKD progression in T2DM
  • No gynecomastia or menstrual effects unlike spironolactone

Safety Profile

Pregnancy avoid
Lactation avoid
Renal Adjustment Required
Hepatic Adjustment Required
TDM Not required
Guideline Update pending

Concordance Terms

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