fosinopril

Brand: Monopril

⚠ BBW Prototype: lisinopril
Drug Class: ACE inhibitor
Drug Family: antihypertensive
Subclass: phosphonate prodrug ACE inhibitor
Organ Systems: cardiovascularrenal

Mechanism of Action

Phosphonate-containing prodrug; converted to fosinoprilat; inhibits ACE.

ACE (angiotensin-converting enzyme)

Indications

  • hypertension
  • heart failure

Contraindications

  • pregnancy
  • ACE-inhibitor angioedema

Adverse Effects

Common

  • cough
  • hyperkalemia
  • dizziness

Serious

  • angioedema
  • AKI
  • teratogenicity

Pharmacokinetics (ADME)

Absorption 36% bioavailability
Distribution moderate
Metabolism hepatic and GI mucosa to fosinoprilat
Excretion 50% renal, 50% fecal (balanced dual excretion)
Half-life 12 hours
Onset 1 hour
Peak 3-6 hours
Duration 24 hours
Protein Binding >97%
Vd moderate

Drug Interactions

Drug / Agent Mechanism Severity
antacids impaired absorption (separate by 2 hours) minor
potassium-sparing diuretics additive hyperkalemia major

Nursing Considerations

  1. Balanced dual excretion makes it preferred in ESRD
  2. Separate dosing from antacids by 2 hours
  3. Monitor BP and electrolytes

Clinical Pearls

  • Only ACE inhibitor with phosphonate binding to ACE active site
  • Balanced 50/50 renal-hepatic clearance preferred in severe CKD/ESRD

Safety Profile

Pregnancy contraindicated
Lactation avoid
Renal Adjustment Not required
Hepatic Adjustment Not required
TDM Not required

Concordance Terms

Cross-referenced clinical concepts — click any term to see all content where it appears.