patiromer

Brand: Veltassa

Prototype Drug
Drug Class: potassium binder
Drug Family: electrolyte agent
Subclass: non-absorbed potassium exchanger (calcium-patiromer)
Organ Systems: renal

Mechanism of Action

Non-absorbed polymer that exchanges calcium for potassium in the GI lumen, reducing potassium absorption; useful for chronic hyperkalemia management.

gastrointestinal potassium exchange (lumen)

Indications

  • hyperkalemia (chronic — especially in CKD with RAAS inhibitor use)

Contraindications

  • bowel obstruction
  • severe constipation

Adverse Effects

Common

  • constipation
  • hypomagnesemia
  • diarrhea

Serious

  • severe hypomagnesemia

Pharmacokinetics (ADME)

Absorption not absorbed (GI-local action)
Distribution GI lumen
Metabolism not applicable — exchanges K+ for Ca2+
Excretion fecal (bound K+)
Half-life not applicable (onset 7h)
Onset 7+ hours
Peak multiple days
Duration days
Protein Binding not applicable
Vd GI lumen

Drug Interactions

Drug / Agent Mechanism Severity
other oral medications patiromer may bind and reduce absorption of other drugs — separate by 3 hours major

Nursing Considerations

  1. Separate other oral medications by at least 3 hours (patiromer binds drugs in GI tract)
  2. Steady state effect requires several days
  3. Monitor K+ and Mg2+ levels
  4. Onset delayed: not for acute hyperkalemia (use calcium gluconate, insulin/dextrose, or sodium bicarb first)
  5. Mix with water; do not heat (alters polymer structure)

Clinical Pearls

  • Unlike sodium polystyrene sulfonate (Kayexalate), patiromer uses calcium-based exchange — less sodium load
  • Approved to allow continuation of RAAS inhibitors in CKD by controlling hyperkalemia

Safety Profile

Pregnancy insufficient-data
Lactation insufficient-data
Renal Adjustment Required
Hepatic Adjustment Not required
TDM Not required
Guideline Update pending

Concordance Terms

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