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Patiromer

VELTASSA

Pronunciation: pa-TIR-oe-mer

Patiromer ballicule: receptor binding, kinetics and half-life diagram
Mechanism of action: Patiromer ballicule
Patiromer VELTASSA mascot mnemonic cartoon
Visual mnemonic: Patiromer mascot
“Trades calcium for K+”

What it isNon-absorbed potassium binder exchanging calcium for potassium; hyperkalemia.

Why this oneIt allows RAAS inhibitors to be continued in heart failure and CKD, which is usually the point of using it.

What limits itOnset takes about seven hours, so it is not for emergencies. It binds other drugs — separate by three hours; hypomagnesemia.

Patiromer molecular structure (skeletal formula)
Molecular structure: Patiromer

FDA label

FDA dosingPopulationStartTargetMax
HyperkalemiaAdults8.4 g QDtitrate by 8.4 g at ≥1-wk intervals25.2 g QD
HyperkalemiaChildren 12–17 yr4 g QDtitrate by 4 g at ≥1-wk intervals25.2 g QD

Titration Adjust at 1-week or longer intervals

Renal No adjustment needed

Hepatic Undefined

Separate from other oral medications by at least 3 hours

Instructions

Available strengths

Cautions

Adverse reactions

Pregnancy Not absorbed systemically; maternal use not expected to result in fetal risk.

Lactation Not absorbed systemically; not expected to result in risk to the infant.

Cost

Patiromer (VELTASSA)
Strength#/mogeneric $/unitCostPlus
1 g/packetpowderper unitnot offered
8.4 g/packetpowderper unitnot offered
16.8 g/packetpowderper unitnot offered
NADAC is a voluntary CMS survey of what retail community pharmacies pay for the drugs they stock. Patiromer is dispensed outside retail pharmacies, so it rarely appears on surveyed invoices.

Generic entry2033 est.

NO BOXED WARNINGS

Principal riskSlow onset; binds other drugs, separate by three hours

Classes and tags

Clinical profile

Therapeutic safety burden1 / 4
Overdose danger1 / 4
Weight-gain liability0 / 4
Sedation liability0 / 4
QT / Torsades0 / 4
Direct muscarinic antagonism0 / 4
Embryofetal risk0 / 4

Legacy pregnancy categoryUnknown / historical label unavailable

Defining liabilityLocal irritation, sensitization or administration-site injury; negligible systemic toxicity at usual use.

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