amiloride

Brand: Midamor

Prototype: spironolactone
Drug Class: potassium-sparing diuretic
Drug Family: diuretic
Subclass: pyrazine-carbonyl guanidine ENaC blocker
Organ Systems: renalcardiovascular

Mechanism of Action

Directly blocks ENaC in collecting duct; mild natriuresis with potassium retention; also used for lithium-induced nephrogenic DI.

epithelial sodium channel (ENaC) in collecting duct

Indications

  • edema (with thiazide/loop)
  • hypokalemia prevention
  • lithium-induced nephrogenic diabetes insipidus (off-label)

Contraindications

  • hyperkalemia
  • severe renal impairment

Adverse Effects

Common

  • hyperkalemia
  • nausea
  • diarrhea
  • headache

Serious

  • severe hyperkalemia

Pharmacokinetics (ADME)

Absorption 15-25% oral
Distribution moderate
Metabolism minimal hepatic — excreted largely unchanged
Excretion renal
Half-life 6-9 hours
Onset 1-4 hours
Peak 6-10 hours
Duration 24 hours
Protein Binding <23%
Vd moderate

Drug Interactions

Drug / Agent Mechanism Severity
ACE inhibitors/ARBs additive hyperkalemia major
NSAIDs reduced efficacy moderate

Nursing Considerations

  1. K+ monitoring essential
  2. Useful in lithium-induced nephrogenic DI (blocks ENaC through which lithium enters principal cells)
  3. Low protein binding — not displaced by other drugs

Clinical Pearls

  • Blocks the channel through which lithium enters renal collecting duct cells — reduces lithium-induced nephrogenic DI
  • Minimal protein binding — few displacement interactions

Safety Profile

Pregnancy use-with-caution
Lactation use-with-caution
Renal Adjustment Required
Hepatic Adjustment Not required
TDM Not required

Concordance Terms

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