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Silodosin

RAPAFLO

Pronunciation: sye-lo-DOE-sin

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

What it isHighly alpha-1A-selective antagonist; benign prostatic hyperplasia.

Why this oneIts exceptional uroselectivity relieves outlet symptoms with less blood-pressure effect than nonselective alpha blockers.

What limits itEjaculatory dysfunction commonly ends treatment; renal impairment requires adjustment, and cataract surgery risks floppy iris.

Silodosin molecular structure (skeletal formula)
Molecular structure: Silodosin

FDA-approved for

FDA label

FDA dosingPopulationStartTargetMax
Benign prostatic hyperplasiaAdult males8 mg QD with a meal8 mg QD8 mg QD

Renal Mild (CCr 50-80): no adjustment; moderate (CCr 30-50): 4 mg QD; severe (<30): contraindicated

Hepatic Mild-moderate: no adjustment; severe (Child-Pugh ≥10): contraindicated

Moderate renal impairment (CCr 30-50 mL/min): reduce to 4 mg QD

Instructions

Available strengths

Contraindications

Cautions

Adverse reactions

Pregnancy Not indicated for use in females

Lactation Not indicated for use in females

Cost

Silodosin (RAPAFLO)
What pharmacies pay · NADAC 9/30/26
Strength#/mogeneric $/moCostPlus
4 mgcap30 qd$7.95offered
8 mgcap30 qd$9.56offered

Generic entry2017

NO BOXED WARNINGS

Principal riskRetrograde ejaculation; intraoperative floppy iris

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 risk1 / 4

Legacy pregnancy categoryC

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

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