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Vericiguat

VERQUVO

Pronunciation: ver-i-SIG-yoo-at (ver-KYOO-voe)

Vericiguat ballicule: receptor binding, kinetics and half-life diagram
Mechanism of action: Vericiguat ballicule

What it isSoluble guanylate cyclase stimulator; heart failure with reduced ejection fraction after a worsening event.

Why this oneUnlike foundational heart-failure drugs, it is reserved for recent decompensation despite standard therapy.

What limits itHypotension and anemia limit use. Avoid other sGC stimulators; PDE5 inhibitors are not recommended. Embryo-fetal toxicity.

Vericiguat molecular structure (skeletal formula)
Molecular structure: Vericiguat

FDA-approved for

FDA label

BOXED WARNING Embryo-fetal toxicity — exclude pregnancy before start; use effective contraception during and 1 month after treatment
FDA dosingPopulationStartTargetMax
Heart failure (reduce CV death/HF hospitalization risk)adult5 mg QD (2.5 mg QD if hypotension risk)10 mg QD10 mg QD

Titration Double dose approximately every 2 weeks to target, as tolerated

Renal Undefined

Hepatic Undefined

Instructions

Available strengths

Contraindications

Cautions

Adverse reactions

Pregnancy Contraindicated; may cause fetal harm

Lactation Breastfeeding not recommended during treatment

Cost

Vericiguat (VERQUVO)
What pharmacies pay · NADAC 9/30/26
Strength#/mogeneric $/mobrand $/moCostPlus
2.5 mgtab30 qd—$681.81not offered
5 mgtab30 qd—$681.81not offered
10 mgtab30 qd—$681.74not offered

Generic entry2032 est.

⚠ BOXED WARNING

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 risk4 / 4

Legacy pregnancy categoryNot assigned — PLLR-era drug

Defining liabilityGenerally tolerated at therapeutic doses; clinically important risks are agent-specific and increase with interactions or organ impairment.

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