Silodosin is a selective alpha-1A adrenergic receptor antagonist used to treat the symptoms of benign prostatic hyperplasia (BPH) in adult men, such as urinary hesitancy, weak stream, frequency, and urgency, by relaxing smooth muscle in the prostate and bladder neck to improve urine flow.[1][2] It does not reduce the size of the prostate or address underlying causes of BPH but provides symptomatic relief without affecting blood pressure significantly due to its receptor selectivity.[3][4]Developed as a uroselective alpha-blocker, silodosin was first approved by the U.S. Food and Drug Administration in October 2008 under the brand name Rapaflo, with subsequent approvals in Europe (as Urorec) in 2010 and other regions.[1] It is available in oral capsule form, typically dosed at 4 mg or 8 mg once daily with food (to reduce peak plasma levels and the risk of orthostatic hypotension), which has an absolute bioavailability of approximately 32%, and has a half-life of about 13 hours, primarily metabolized via glucuronidation by UGT2B7 and partially by CYP3A4.[1][4] Clinical studies have demonstrated its efficacy, with significant improvements in the International Prostate Symptom Score (IPSS) compared to placebo, such as a 6.4-point reduction after 12 weeks versus 3.5 points for placebo.[4]Common side effects include abnormal ejaculation (often retrograde, affecting semen volume in over 10% of users), dizziness, diarrhea, and nasal congestion, while serious risks involve orthostatic hypotension and intraoperative floppy iris syndrome during cataract surgery.[2][4] Silodosin is contraindicated in severe renal or hepatic impairment and should be used cautiously with CYP3A4 inhibitors like ketoconazole, which can increase its exposure.[1][3] It is not indicated for women or hypertension and requires discontinuation before eye surgery.[2]
Clinical applications
Indications
Silodosin is indicated for the treatment of the signs and symptoms of benign prostatic hyperplasia (BPH) in adult men, including irritative symptoms such as urinary frequency, urgency, and nocturia, as well as obstructive symptoms like hesitancy, weak stream, intermittency, and incomplete emptying.[5] It is not indicated for the treatment of hypertension or for use in women.[5][1]The recommended initial dosage is 8 mg orally once daily, administered with a meal to reduce the risk of adverse effects.[5] In patients with moderate renal impairment (creatinine clearance of 30–50 mL/min), the dosage should be reduced to 4 mg once daily with a meal, while it is contraindicated in severe renal impairment (creatinine clearance <30 mL/min).[5]Clinical trials have shown that silodosin significantly improves the International Prostate Symptom Score (IPSS), with mean reductions of 6.3 to 6.5 points from baseline after 12 weeks compared to 3.4 to 3.6 points with placebo (p<0.0001), and improvements observable as early as day 1 of treatment.[5]Although not approved for this purpose, silodosin has been investigated off-label for medical expulsive therapy in patients with distal ureteral stones, where it may facilitate stone passage.[6]
Contraindications
Silodosin is contraindicated in patients with known hypersensitivity to the drug or any of its excipients, as severe allergic reactions may occur.[7] It is also absolutely contraindicated in individuals with severe renal impairment, defined as creatinine clearance (CrCl) less than 30 mL/min, due to significantly elevated plasma concentrations and increased risk of adverse effects.[7] Similarly, use is prohibited in patients with severe hepatic impairment (Child-Pugh class C, score >10), where drug metabolism is substantially compromised, leading to potential toxicity.[7] Following the approval of nirmatrelvir/ritonavir (Paxlovid) in late 2021, concomitant administration with silodosin has been contraindicated due to ritonavir's potent CYP3A4 inhibition, which can cause profound increases in silodosin exposure and severe orthostatic hypotension.[8]Relative contraindications include moderate renal impairment (CrCl 30-50 mL/min) or moderate hepatic impairment (Child-Pugh class B), where dose reduction to 4 mg daily is required to mitigate accumulation risks, with close monitoring advised.[7] Concurrent use with other alpha-1 blockers, such as doxazosin or terazosin, is relatively contraindicated owing to additive effects on blood pressure and heightened hypotension risk.[9]Precautions are necessary for elderly patients or those receiving antihypertensive therapy, as silodosin may exacerbate orthostatic hypotension, particularly upon initiation; patients should be advised to rise slowly from sitting or lying positions.[7] Additionally, men planning cataract surgery should inform their ophthalmologist of silodosin use, as it is associated with intraoperative floppy iris syndrome (IFIS), which can complicate procedures despite discontinuation weeks prior.[7] Baseline assessment of renal function via CrCl estimation is recommended before starting therapy to identify at-risk patients.[7]
Safety profile
Adverse effects
Silodosin is generally well-tolerated, but adverse effects are primarily related to its alpha-1A adrenergic antagonism. The most common adverse effect is abnormal ejaculation, manifesting as retrograde ejaculation or reduced ejaculate volume, with an incidence of up to 28.1% in placebo-controlled clinical trials; this effect is dose-dependent, occurs more frequently at higher doses, and is reversible upon discontinuation of the drug.[10]Cardiovascular adverse effects include orthostatic hypotension (2.6%), dizziness (3.2%), and syncope (<1%), which may pose risks particularly in elderly patients or those with comorbidities.[10]Other frequent adverse effects reported in 1-3% of patients include headache (2.4%), nasal congestion (2.1%), and diarrhea (2.6%).[10]
Adverse Effect
Incidence (Silodosin)
Incidence (Placebo)
Abnormal ejaculation
28.1%
0.9%
Dizziness
3.2%
1.1%
Diarrhea
2.6%
1.3%
Orthostatic hypotension
2.6%
1.5%
Headache
2.4%
0.9%
Nasal congestion
2.1%
0.2%
Serious or rare adverse effects include intraoperative floppy iris syndrome (IFIS), which increases surgical complications during cataract procedures and has been reported in isolated cases with silodosin use; priapism, a prolonged erection requiring urgent medical attention, occurring very rarely (one case in clinical trials); and allergic reactions such as rash, pruritus, or angioedema.[10][11][12]In long-term studies extending up to 52 weeks, silodosin demonstrated low hepatotoxicity potential, with no subjects having ALT ≥3-5x ULN in controlled trials and no clear causal link in post-marketing reports.[10][13]Discontinuation rates due to adverse events in Phase 3 clinical trials were 12.9% for silodosin vs. 4.3% for placebo, with abnormal ejaculation accounting for 2.7% of cases.[10]
Drug interactions
Silodosin is primarily metabolized via glucuronidation by UGT2B7, with partial metabolism by CYP3A4, and co-administration with strong CYP3A4 inhibitors such as ketoconazole or ritonavir can significantly increase silodosin exposure. For instance, concomitant use with 400 mg ketoconazole results in a 3.8-fold increase in Cmax and a 3.2-fold increase in AUC of silodosin, while 200 mg ketoconazole leads to a 3.7-fold increase in Cmax and 2.9-fold increase in AUC.[5] Strong CYP3A4 inhibitors are contraindicated with silodosin due to the risk of enhanced adverse effects.[5] Moderate CYP3A4 inhibitors, such as diltiazem, increase silodosin AUC by approximately 30%, necessitating a reduction in silodosin dose to 4 mg daily or close monitoring for adverse effects.[5]Silodosin may interact pharmacodynamically with phosphodiesterase-5 (PDE5) inhibitors like sildenafil, potentially leading to additive hypotensive effects due to combined vasodilation.[5] However, clinical studies have shown no significant orthostatic hypotension when silodosin is co-administered with sildenafil or tadalafil, though caution is advised, particularly with higher doses of PDE5 inhibitors, and no dose adjustment is typically required.[14]Combination with other alpha-blockers, such as tamsulosin or doxazosin, can produce additive effects on blood pressure lowering, increasing the risk of symptomatic hypotension.[5] Such combinations should be avoided.[5]When used with antihypertensives, silodosin does not appear to cause substantial additional hypotension, as evidenced by phase 3 clinical trials where the incidence of orthostatic hypotension was comparable to placebo in patients on concomitant antihypertensive therapy.[5] Nonetheless, blood pressure monitoring is recommended during initiation of therapy.[5]Silodosin is a substrate for P-glycoprotein (P-gp), and strong P-gp inhibitors such as cyclosporine or ritonavir may increase silodosin plasma concentrations, potentially enhancing exposure and adverse effects.[5] Co-administration with strong P-gp inhibitors is not recommended, and patients should be monitored if unavoidable.[5]No clinically significant pharmacokinetic interactions have been observed between silodosin and warfarin or digoxin.[5] Regarding food, silodosin should be taken with a meal to improve absorption and reduce variability in exposure, though high-fat meals can decrease Cmax by 18-43% and AUC by 4-49% without altering overall efficacy.[5]
Pharmacology
Mechanism of action
Silodosin acts as a selective antagonist at the α<sub>1A</sub>-adrenergic receptors, exhibiting a markedly higher affinity for this subtype compared to the α<sub>1B</sub> and α<sub>1D</sub> subtypes. Specifically, its affinity for the α<sub>1A</sub> receptor is approximately 583-fold greater than for the α<sub>1B</sub> receptor and 56-fold greater than for the α<sub>1D</sub> receptor, enabling targeted blockade without substantial interference with other adrenergic pathways.[15] This selectivity is a key feature distinguishing silodosin from less specific α<sub>1</sub>-blockers, as the α<sub>1A</sub> receptors are the predominant subtype in the lower urinary tract.[15]The α<sub>1A</sub>-adrenergic receptors are primarily located in the smooth muscle of the prostate stroma, bladder neck, and urethra, where they mediate contraction in response to sympathetic stimulation. By competitively antagonizing these receptors, silodosin inhibits norepinephrine-induced contraction, leading to relaxation of the smooth muscle in these regions. This relaxation reduces dynamic obstruction at the bladder outlet, facilitating improved urine flow—typically increasing maximum urinary flow rate (Q<sub>max</sub>) by 2–3 mL/s—and alleviating lower urinary tract symptoms associated with benign prostatic hyperplasia.[16][17] Unlike 5α-reductase inhibitors, silodosin exerts no direct effect on prostate size, providing symptomatic relief through functional rather than structural changes.[18]Silodosin's uroselectivity stems from its minimal interaction with α<sub>1B</sub>-adrenergic receptors, which are more abundant in vascular smooth muscle and responsible for blood pressure regulation. This profile results in negligible effects on vascular tone, with orthostatic hypotension occurring in less than 3% of patients, a rate comparable to placebo and lower than that observed with non-selective α<sub>1</sub>-blockers. Consequently, silodosin offers a favorable cardiovascular safety margin, making it suitable for patients with comorbidities involving blood pressure stability.[19][20]
Pharmacokinetics
Silodosin is administered orally and exhibits an absolute bioavailability of approximately 32%. [5] Following a single 8 mg dose taken with a meal, peak plasma concentrations (C_max) are reached at a median time (T_max) of 2.6 hours, with steady-state C_max values of about 62 ng/mL and area under the curve (AUC) of 373 ng·h/mL. [5] The pharmacokinetics are linear over the therapeutic dose range of 4-8 mg daily. [21] Administration with food, as recommended to minimize the risk of orthostatic hypotension, decreases C_max by 18-43% and AUC by 4-49% compared to the fasted state, while delaying T_max by approximately 1 hour; however, these changes do not alter the overall bioavailability. [5]The apparent volume of distribution at steady state is 49.5 L, indicating moderate tissue distribution. [22] Silodosin is highly bound to plasma proteins, primarily alpha-1 acid glycoprotein, with approximately 97% binding. [5] It demonstrates good penetration into prostatic tissue, achieving concentrations several-fold higher than in plasma, which supports its therapeutic effects in the prostate. [15]Silodosin undergoes extensive hepatic metabolism primarily through glucuronidation by UGT2B7, as well as oxidation via CYP3A4 and activity of alcohol and aldehyde dehydrogenases. [21] The major metabolite, silodosin glucuronide (KMD-3213G), is pharmacologically active with affinity for alpha-1A adrenoceptors comparable to the parent compound and exhibits plasma exposure approximately four times higher, with a half-life of about 24 hours. [22] A secondary metabolite, KMD-3293 (formed via dehydrogenation), has similar exposure to silodosin but minimal pharmacologic activity. [5]Elimination of silodosin occurs primarily via feces, with 54.9% of the dose recovered there and 33.5% in urine over 10 days following oral administration of radiolabeled drug; unchanged silodosin accounts for less than 0.5% of the urinary excretion. [5] The terminal elimination half-life of the parent compound is 13.3 hours at steady state, with plasma clearance of approximately 10 L/h. [22]Steady-state concentrations are achieved within four days of daily dosing. [15]In special populations, exposure is slightly higher in elderly men, with AUC increased by about 15% and half-life prolonged by 20% compared to younger adults, though no dose adjustment is required. [5] Renal impairment significantly affects pharmacokinetics: in moderate impairment (creatinine clearance 30-50 mL/min), AUC and C_max increase approximately 3-fold, necessitating a reduced starting dose of 4 mg; the drug is contraindicated in severe impairment (creatinine clearance <30 mL/min). [21] For hepatic impairment, no clinically significant changes occur in mild to moderate cases (Child-Pugh A or B), and dose adjustment is unnecessary; it is contraindicated in severe impairment (Child-Pugh C). [22]
History and regulation
Development and approvals
Silodosin was developed by Kissei Pharmaceutical Co., Ltd. in Japan starting in the early 1990s as a highly selective uroselective α1A-adrenoceptor antagonist aimed at treating lower urinary tract symptoms associated with benign prostatic hyperplasia (BPH).[16] The compound was designed to minimize cardiovascular side effects common with less selective alpha-blockers by targeting prostate-specific receptors.[23]Clinical development progressed through phase III trials in the 2000s, including studies in Japan and multinational efforts. In a Japanese phase III trial involving 354 patients, silodosin at 4 mg or 8 mg daily demonstrated significant superiority over placebo in reducing International Prostate Symptom Score (IPSS) by approximately 6-7 points after 12 weeks, alongside improvements in quality of life scores and uroflowmetry parameters.[24] Similar results were observed in two U.S.-based phase III trials with 923 patients, where silodosin 8 mg once daily reduced total IPSS by 6.4 points versus 3.8 points for placebo at 12 weeks, confirming its efficacy and tolerability.[16]Regulatory approvals began in Japan on January 23, 2006, where silodosin was launched as Urief by Kissei in collaboration with Daiichi Sankyo Co., Ltd. in May 2006.[25][23] The U.S. Food and Drug Administration (FDA) approved it in October 2008 under the brand name Rapaflo, marketed by Watson Pharmaceuticals (later Allergan and AbbVie).[26] In the European Union, marketing authorization was granted by the European Medicines Agency on January 29, 2010, as Urorec by Recordati, valid across member states (with Silodyx used for some national authorizations).[27][21]Health Canada issued the Notice of Compliance on January 28, 2011, also as Rapaflo.[28]Post-approval developments included updates to labeling for use in patients with renal impairment; the FDA revised recommendations in subsequent years to allow a reduced 4 mg daily dose for moderate renal impairment (creatinine clearance 30-50 mL/min), based on pharmacokinetic data showing increased exposure in such patients.[5] The original U.S. patent (No. 5,387,603) expired on December 1, 2018, paving the way for generic entry.[29] The first generic silodosin capsules (4 mg and 8 mg) were launched in the U.S. by Lupin Ltd. in December 2018, followed by approvals for other manufacturers like Alembic Pharmaceuticals in 2019.[30]
Legal status
Silodosin is classified as a prescription-only medication worldwide and is not designated as a controlled substance in any major regulatory jurisdiction.[31][32][4]In the United States, silodosin received FDA approval in October 2008 for the treatment of benign prostatic hyperplasia symptoms, with generic versions first approved in 2017 and first made available (launched) in December 2018; it has no history of Class 1 recalls.[26][33][30][34]Within the European Union, silodosin is authorized by the European Medicines Agency since January 29, 2010, under the brand Urorec, with prescription requirements enforced across member states and reimbursement status varying by national health systems.[27][35]In Japan, silodosin was approved on January 23, 2006, for benign prostatic hyperplasia under the brand Urief and remains available exclusively by prescription, with no over-the-counter status.[36][25]Silodosin is approved for use in over 50 countries globally, including Canada, Australia, and several in Asia and Latin America, though access may be restricted in some regions due to high costs or limited market authorization.[37][38]As of November 2025, there have been no changes to silodosin's regulatory classification or approval status worldwide, though its prescribing information continues to be monitored for updates related to interactions with nirmatrelvir-ritonavir (Paxlovid), which is contraindicated due to increased silodosin exposure risks; intermittent drug shortages have been reported in the US.[39][40][41]
Society and culture
Brand names
Silodosin is marketed under several brand names worldwide, with variations depending on the region. In the United States, it was previously available as Rapaflo (discontinued around 2022), developed by Kissei Pharmaceutical and marketed by Allergan (now part of AbbVie). In Japan, the brand name is Urief, marketed by Kissei Pharmaceutical. In the European Union, it is sold as Urorec or Silodyx by Recordati.[21][27]Generic versions of silodosin are available in capsule form at strengths of 4 mg and 8 mg. In the United States, generics are produced by manufacturers such as Lupin Pharmaceuticals and Alembic Pharmaceuticals.[30] In India, examples include Silofast, manufactured by Cipla.[42]No fixed-dose combination products containing silodosin have been approved; it is available only as a standalone medication.[1]Brand names for silodosin often emphasize its uroselective properties as an alpha-1A adrenergic receptor antagonist, targeting lower urinary tract symptoms associated with benign prostatic hyperplasia.
Availability
Silodosin is widely available in North America, Europe, and Asia due to regulatory approvals from key agencies, including the U.S. Food and Drug Administration (FDA) in 2008 for the brand Rapaflo (now discontinued), the European Medicines Agency (EMA) for Silodosin Recordati, and Japan's Pharmaceuticals and Medical Devices Agency (PMDA) in 2006 for Urief.[4][43] Market reports indicate strong penetration in these regions, driven by aging populations and increasing benign prostatic hyperplasia (BPH) diagnoses, with North America holding about 35% of the global market share, Europe 30%, and Asia-Pacific 25%.[44]Availability remains limited in Africa and Latin America, where market shares are smaller at around 5% combined, reflecting slower healthcare infrastructuredevelopment and fewer regulatory approvals, though gradual expansion is occurring through imports and emerging local manufacturing.[44][45]In the United States, generic competition began following patent expiry on December 1, 2018, with the first generics launched in December 2018, significantly reducing costs to around $15-25 for a 30-day supply of 8 mg capsules (as of 2025), or an annual cost of $200-500 depending on dosage and pharmacy.[46][47][48][49]In Japan and the European Union, silodosin is primarily available as branded formulations, with monthly costs around $50 for standard dosing; insurance coverage varies but often offsets a portion in national health systems, such as Japan's National Health Insurance or EU public payers.[50]Affordable generic versions dominate in India and China, where monthly costs are approximately $10 or less for 8 mg capsules, supported by robust local production and compulsory licensing provisions that enhance access in these high-volume emerging markets.[51][52]No significant supply disruptions for silodosin have been reported since the COVID-19 pandemic, with global supply chains stabilizing by 2023 due to diversified manufacturing and steady API production.[45]
Research
Ongoing clinical studies
A 2025 comprehensive review of clinical evidence confirmed silodosin's efficacy in treating benign prostatic hyperplasia (BPH), including in patients with cardiovascular comorbidities, with significant improvements in the International Prostate Symptom Score (IPSS) ranging from 7 to 12 points across studies and a favorable tolerability profile characterized by mild adverse events.[53]As of late 2025, ongoing clinical trials for silodosin remain primarily adult-focused, with no active studies identified in pediatric or adolescent populations. A phase III trial (NCT07146386) is evaluating the efficacy and safety of silodosin compared to a sustained-release alternative for BPH symptom relief, building on established short-term data. Long-term safety extensions, such as prior 9-month open-label studies demonstrating sustained IPSS reductions and low discontinuation rates due to adverse events (under 5%), inform current protocols, though no new 3-year extensions are actively recruiting.[54][53]Combination therapy investigations continue for severe BPH, including observational assessments of silodosin paired with 5-alpha-reductase inhibitors (5-ARIs), which show enhanced symptom control and prostate volume reduction without increased cardiovascular risks. Post-marketing surveillance data from regulatory bodies like the FDA and EMA, including a large Japanesecohort, report real-world adverse events at an overall rate of 8.1%, with serious events below 0.1% and no new safety signals beyond known ejaculatory disorders.[55][56]
Emerging indications
Silodosin has been investigated for its potential as a non-hormonal male contraceptive due to its ability to induce anejaculation or retrograde ejaculation, which prevents sperm delivery during intercourse.[57] Studies between 2009 and 2023, including a 2019 prospective double-blind, randomized, placebo-controlled trial, demonstrated that silodosin at 8 mg achieved reversible azoospermia in participants, preventing unintended pregnancies in their partners without altering semen parameters or hormone levels.[58] However, retrograde ejaculation occurred in approximately 28% of users, often accompanied by discomfort such as pelvic pain or reduced sexual satisfaction, which has limited its clinical viability.[59] Despite promising small-scale trials showing no pregnancies when taken 3 hours prior to intercourse, no Phase III studies have advanced this application to approval as of 2025; however, an ongoing randomized trial (NCT07195097, initiated September 2025) is assessing silodosin versus placebo in 200 healthy, sexually active men for on-demand contraception via anejaculation.[57][60]In the management of ureteral stones, silodosin serves as an adjunctive medical expulsive therapy (MET) by relaxing ureteral smooth muscle through alpha-1A receptor blockade, facilitating stone passage.[61] Meta-analyses of randomized controlled trials indicate that silodosin significantly increases stone expulsion rates by 20-30% compared to placebo, with odds ratios ranging from 3.0 to 3.3 for distal stones smaller than 10 mm, while also reducing expulsion time and analgesic requirements.[62] Compared to other alpha-blockers like tamsulosin, silodosin shows superior efficacy for stones under 1 cm, though overall complication rates remain similar.[63] As of 2025, ongoing studies in Asia, particularly in India and Japan, continue to evaluate its role in lithiasis management post-extracorporeal shock wave lithotripsy, but no new regulatory approvals for this indication have been granted globally.[64][65]Pilot studies have explored silodosin for chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS), leveraging its selective alpha-1A blockade to alleviate pain and voiding symptoms by reducing prostate and pelvic smooth muscle tension.[6] A 2011 Phase II multicenter, double-blind, placebo-controlled trial involving men with moderate to severe abacterial CP/CPPS found that silodosin at 4 mg daily significantly improved National Institutes of Health Chronic Prostatitis Symptom Index (NIH-CPSI) scores and quality of life at 4 weeks compared to placebo.[66] However, benefits waned by 12 weeks, and the 8 mg dose showed no significant advantage over placebo, leading to mixed results across studies that highlight short-term relief but inconsistent long-term efficacy.[67]Exploratory investigations into silodosin for female lower urinary tract symptoms (LUTS) are limited by its prostate-specific mechanism, yet off-label use has been assessed for voiding dysfunction and overactive bladder symptoms.[68] A 2023 observational study reported that silodosin improved failure-to-void symptoms in females with LUTS, with side effects occurring in only 11.76% of patients, suggesting tolerability despite the lack of prostate targets.[68] Small trials, including a 2022 single-arm study in bladderpainsyndrome/interstitial cystitis, indicated reductions in pain and urinary frequency, but evidence remains preliminary and not supported by large-scale randomized data.[69] As of November 2025, no approvals extend to female indications, and research continues to be investigational.[70]