Related Experiment Video
Updated: May 10, 2026

Porous Silicon Microparticles for Delivery of siRNA Therapeutics
Published on: January 15, 2015
Silodosin effectively treats benign prostatic hyperplasia symptoms, offering uroselectivity and convenient once-daily dosing. Clinical trials confirm its efficacy and safety, with minimal cardiovascular effects and manageable side effects like retrograde ejaculation.
Area of Science:
- Pharmacology
- Urology
Context:
- Benign prostatic hyperplasia (BPH) affects a significant number of aging men.
- Alpha1A-adrenoceptor antagonists are a cornerstone of BPH pharmacotherapy.
- Existing treatments may have limitations in efficacy or side effect profiles.
Purpose:
- To evaluate the efficacy and safety of silodosin for treating lower urinary tract symptoms (LUTS) associated with BPH.
- To compare silodosin's effectiveness against placebo and tamsulosin.
Summary:
- Silodosin, a selective alpha1A-adrenoceptor antagonist, demonstrated significant improvement in International Prostate Symptom Score (IPSS) total, storage, and voiding subscores compared to placebo (p < 0.001).
- It was found to be at least as effective as tamsulosin (0.4 mg QD) and superior in simultaneously improving specific bothersome LUTS like incomplete emptying, frequency, and nocturia (p = 0.03).
- Phase 3 trials involving over 800 patients showed silodosin (8 mg QD) is well-tolerated, with minimal cardiovascular effects and a manageable rate of retrograde ejaculation (3.9% discontinuation).
Impact:
- Silodosin offers a valuable therapeutic option for BPH management with advantages in uroselectivity and dosing convenience.
- Its favorable safety profile, including minimal cardiovascular impact, allows for concomitant use with other medications.
- Patient education regarding potential side effects like intraocular floppy iris syndrome is crucial for safe and effective treatment.
Related Concept Videos
Antihypertensive Drugs: Vasodilators
Antihypertensive Drugs: Direct Renin Inhibitors
Antihypertensive Drugs: Thiazide-Class Diuretics
Antihypertensive Drugs: Potassium-Sparing Diuretics
Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment
Antihypertensive Drugs: Angiotensin-Converting Enzyme Inhibitors