triamterene

Brand: Dyrenium

Prototype: spironolactone
Drug Class: potassium-sparing diuretic
Drug Family: diuretic
Subclass: pteridine-derivative ENaC blocker
Organ Systems: renalcardiovascular

Mechanism of Action

Directly blocks ENaC in the collecting duct reducing sodium reabsorption without requiring aldosterone binding; mild diuresis, K+ sparing.

epithelial sodium channel (ENaC) in collecting duct

Indications

  • edema
  • hypokalemia prevention (combination with thiazides)

Contraindications

  • hyperkalemia
  • severe renal impairment
  • liver disease

Adverse Effects

Common

  • hyperkalemia
  • crystalluria (triamterene stones)
  • nausea
  • GI upset

Serious

  • severe hyperkalemia
  • renal stones (triamterene)
  • megaloblastic anemia (folate antagonism)

Pharmacokinetics (ADME)

Absorption 30-70% oral (variable)
Distribution moderate
Metabolism hepatic
Excretion renal
Half-life 1.5-2.5 hours
Onset 2-3 hours
Peak 6 hours
Duration 12-16 hours
Protein Binding 67%
Vd moderate

Drug Interactions

Drug / Agent Mechanism Severity
ACE inhibitors/ARBs additive hyperkalemia major
NSAIDs AKI risk (especially indomethacin) major
cimetidine inhibits renal secretion of triamterene — increases levels moderate

Nursing Considerations

  1. Monitor K+ and renal function
  2. Triamterene can crystallize in urine — maintain hydration
  3. Often combined with HCTZ (Dyazide, Maxzide) to prevent hypokalemia
  4. Folate antagonist — megaloblastic anemia in folate-deficient patients

Clinical Pearls

  • ENaC blocker: potassium-sparing without aldosterone antagonism — works when spironolactone does not
  • Triamterene kidney stones: unique among diuretics
  • Weak diuretic alone — used primarily for K+ protection

Safety Profile

Pregnancy avoid
Lactation avoid
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.