General Information of Drug (ID: DM5QF9V)

Drug Name
Tamsulosin
Synonyms
Flomax; Flowmax; Harnal; Tamsolusin; Tamsulon; Tamsulosina; Tamsulosine; Tamsulosinum; Flomax (TN); Flomaxtra (TN); Tamsulon (TN); Tamsulosin (INN); Tamsulosin [INN:BAN]; Tamsulosina [INN-Spanish]; Tamsulosine [INN-French]; Tamsulosinum [INN-Latin]; Urimax (TN); (R)-5-(2-((2-(2-Ethoxyphenoxy)ethyl)amino)propyl)-2-methoxybenzenesulfonamide; 5-(2-((2-(2-ethoxyphenoxy)ethyl)amino)propyl)-2-methoxybenzenesulfonamide; 5-[(2R)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]-2-methoxybenzenesulfonamide; 5-[(2R)-2-{[2-(2-ethoxyphenoxy)ethyl]amino}propyl]-2-methoxybenzenesulfonamide; 5-[2-[2-(2-ethoxyphenoxy)ethylamino]propyl]-2-methoxy-benzenesulfonamide; 5-{(2R)-2-[(2-{[2-(ethyloxy)phenyl]oxy}ethyl)amino]propyl}-2-(methyloxy)benzenesulfonamide
Indication
Disease Entry ICD 11 Status REF
Benign prostatic hyperplasia GA90 Approved [1]
Urinary retention MF50.3 Approved [2]
Therapeutic Class
Anticancer Agents
Drug Type
Small molecular drug
Structure
3D MOL 2D MOL
#Ro5 Violations (Lipinski): 1 Molecular Weight (mw) 408.5
Logarithm of the Partition Coefficient (xlogp) 2.7
Rotatable Bond Count (rotbonds) 11
Hydrogen Bond Donor Count (hbonddonor) 2
Hydrogen Bond Acceptor Count (hbondacc) 7
ADMET Property
BDDCS Class
Biopharmaceutics Drug Disposition Classification System (BDDCS) Class 1: high solubility and high permeability [3]
Bioavailability
99% of drug becomes completely available to its intended biological destination(s) [4]
Clearance
The clearance of drug is 2.88 L/h []
Elimination
97% of an orally administered does is recovered in studies, which 76% in the urine and 21% in the feces after 168 hours. 8.7% of the dose is excreted as unmetabolized tamsulosin [5]
Half-life
The concentration or amount of drug in body reduced by one-half in 14.9 +/- 3.9 hours [6]
Metabolism
The drug is metabolized via the liver [7]
MRTD
The Maximum Recommended Therapeutic Dose (MRTD) of drug that ensured maximising efficacy and moderate side effect is 0.03256 micromolar/kg/day [8]
Unbound Fraction
The unbound fraction of drug in plasma is 0.01% [6]
Vd
The volume of distribution (Vd) of drug is 16 L []
Chemical Identifiers
Formula
C20H28N2O5S
IUPAC Name
5-[(2R)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]-2-methoxybenzenesulfonamide
Canonical SMILES
CCOC1=CC=CC=C1OCCN[C@H](C)CC2=CC(=C(C=C2)OC)S(=O)(=O)N
InChI
InChI=1S/C20H28N2O5S/c1-4-26-17-7-5-6-8-18(17)27-12-11-22-15(2)13-16-9-10-19(25-3)20(14-16)28(21,23)24/h5-10,14-15,22H,4,11-13H2,1-3H3,(H2,21,23,24)/t15-/m1/s1
InChIKey
DRHKJLXJIQTDTD-OAHLLOKOSA-N
Cross-matching ID
PubChem CID
129211
ChEBI ID
CHEBI:9398
CAS Number
106133-20-4
DrugBank ID
DB00706
TTD ID
D05MBZ
INTEDE ID
DR1530
ACDINA ID
D00651
Combinatorial Drugs (CBD) Click to Jump to the Detailed CBD Information of This Drug
Repurposed Drugs (RPD) Click to Jump to the Detailed RPD Information of This Drug

Molecular Interaction Atlas of This Drug


Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Adrenergic receptor alpha-1A (ADRA1A) TTNGILX ADA1A_HUMAN Modulator [9]

Drug-Metabolizing Enzyme (DME)
DME Name DME ID UniProt ID MOA REF
Cytochrome P450 3A4 (CYP3A4)
Main DME
DE4LYSA CP3A4_HUMAN Substrate [10]
Cytochrome P450 2D6 (CYP2D6)
Main DME
DECB0K3 CP2D6_HUMAN Substrate [10]

Drug Off-Target (DOT)
DOT Name DOT ID UniProt ID Interaction REF
Alpha-1A adrenergic receptor (ADRA1A) OTUIWCL5 ADA1A_HUMAN Protein Interaction/Cellular Processes [11]
Phosphatidylcholine translocator ABCB4 (ABCB4) OTE6PY83 MDR3_HUMAN Gene/Protein Processing [12]
Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This Drug

Molecular Expression Atlas of This Drug

The Studied Disease Benign prostatic hyperplasia
ICD Disease Classification GA90
Molecule Name Molecule Type Gene Name p-value Fold-Change Z-score
Adrenergic receptor alpha-1A (ADRA1A) DTT ADRA1A 9.43E-01 -0.03 -0.25
Cytochrome P450 2D6 (CYP2D6) DME CYP2D6 5.64E-01 2.36E-02 1.75E-01
Cytochrome P450 3A4 (CYP3A4) DME CYP3A4 6.06E-01 -2.42E-02 -1.64E-01
Molecular Expression Atlas (MEA) Jump to Detail Molecular Expression Atlas of This Drug

Drug-Drug Interaction (DDI) Information of This Drug

Coadministration of a Drug Treating the Same Disease as Tamsulosin
DDI Drug Name DDI Drug ID Severity Mechanism Disease REF
Terazosin DM3JCVS Moderate Additive hypotensive effects by the combination of Tamsulosin and Terazosin. Prostate hyperplasia [GA90] [13]
Silodosin DMJSBT6 Moderate Additive hypotensive effects by the combination of Tamsulosin and Silodosin. Prostate hyperplasia [GA90] [13]
Coadministration of a Drug Treating the Disease Different from Tamsulosin (Comorbidity)
DDI Drug Name DDI Drug ID Severity Mechanism Comorbidity REF
Arn-509 DMT81LZ Moderate Increased metabolism of Tamsulosin caused by Arn-509 mediated induction of CYP450 enzyme. Acute myeloid leukaemia [2A60] [14]
Dronedarone DMA8FS5 Moderate Decreased metabolism of Tamsulosin caused by Dronedarone mediated inhibition of CYP450 enzyme. Angina pectoris [BA40] [15]
Posaconazole DMUL5EW Major Decreased metabolism of Tamsulosin caused by Posaconazole mediated inhibition of CYP450 enzyme. Aspergillosis [1F20] [16]
Dalfopristin DM4LTKV Moderate Decreased metabolism of Tamsulosin caused by Dalfopristin mediated inhibition of CYP450 enzyme. Bacterial infection [1A00-1C4Z] [15]
Clarithromycin DM4M1SG Major Decreased metabolism of Tamsulosin caused by Clarithromycin mediated inhibition of CYP450 enzyme. Bacterial infection [1A00-1C4Z] [16]
Troleandomycin DMUZNIG Major Decreased metabolism of Tamsulosin caused by Troleandomycin mediated inhibition of CYP450 enzyme. Bacterial infection [1A00-1C4Z] [16]
Telithromycin DMZ4P3A Major Decreased metabolism of Tamsulosin caused by Telithromycin mediated inhibition of CYP450 enzyme. Bacterial infection [1A00-1C4Z] [16]
Cariprazine DMJYDVK Moderate Additive hypotensive effects by the combination of Tamsulosin and Cariprazine. Bipolar disorder [6A60] [17]
Pexidartinib DMS2J0Z Moderate Increased metabolism of Tamsulosin caused by Pexidartinib mediated induction of CYP450 enzyme. Bone/articular cartilage neoplasm [2F7B] [18]
Tucatinib DMBESUA Major Decreased metabolism of Tamsulosin caused by Tucatinib mediated inhibition of CYP450 enzyme. Breast cancer [2C60-2C6Y] [16]
Mifepristone DMGZQEF Moderate Decreased metabolism of Tamsulosin caused by Mifepristone mediated inhibition of CYP450 enzyme. Cushing syndrome [5A70] [16]
MK-8228 DMOB58Q Moderate Decreased metabolism of Tamsulosin caused by MK-8228 mediated inhibition of CYP450 enzyme. Cytomegaloviral disease [1D82] [15]
Sertraline DM0FB1J Moderate Decreased metabolism of Tamsulosin caused by Sertraline mediated inhibition of CYP450 enzyme. Depression [6A70-6A7Z] [15]
Nefazodone DM4ZS8M Major Decreased metabolism of Tamsulosin caused by Nefazodone mediated inhibition of CYP450 enzyme. Depression [6A70-6A7Z] [16]
Paroxetine DM5PVQE Moderate Decreased metabolism of Tamsulosin caused by Paroxetine mediated inhibition of CYP450 enzyme. Depression [6A70-6A7Z] [15]
Selegiline DM6034S Moderate Additive hypotensive effects by the combination of Tamsulosin and Selegiline. Depression [6A70-6A7Z] [19]
Isocarboxazid DMAF1NB Moderate Additive hypotensive effects by the combination of Tamsulosin and Isocarboxazid. Depression [6A70-6A7Z] [19]
Tranylcypromine DMGB5RE Moderate Additive hypotensive effects by the combination of Tamsulosin and Tranylcypromine. Depression [6A70-6A7Z] [19]
OPC-34712 DMHG57U Moderate Additive hypotensive effects by the combination of Tamsulosin and OPC-34712. Depression [6A70-6A7Z] [17]
Phenelzine DMHIDUE Moderate Additive hypotensive effects by the combination of Tamsulosin and Phenelzine. Depression [6A70-6A7Z] [19]
Cenobamate DM8KLU9 Moderate Increased metabolism of Tamsulosin caused by Cenobamate mediated induction of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [20]
Stiripentol DMMSDOY Moderate Decreased metabolism of Tamsulosin caused by Stiripentol mediated inhibition of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [15]
Mirabegron DMS1GYT Moderate Decreased metabolism of Tamsulosin caused by Mirabegron mediated inhibition of CYP450 enzyme. Functional bladder disorder [GC50] [21]
Itraconazole DMCR1MV Major Decreased metabolism of Tamsulosin caused by Itraconazole mediated inhibition of CYP450 enzyme. Fungal infection [1F29-1F2F] [16]
Terbinafine DMI6HUW Moderate Decreased metabolism of Tamsulosin caused by Terbinafine mediated inhibition of CYP450 enzyme. Fungal infection [1F29-1F2F] [15]
Miconazole DMPMYE8 Moderate Decreased metabolism of Tamsulosin caused by Miconazole mediated inhibition of CYP450 enzyme. Fungal infection [1F29-1F2F] [15]
Ketoconazole DMPZI3Q Major Decreased metabolism of Tamsulosin caused by Ketoconazole mediated inhibition of CYP450 enzyme. Fungal infection [1F29-1F2F] [16]
Boceprevir DMBSHMF Major Decreased metabolism of Tamsulosin caused by Boceprevir mediated inhibition of CYP450 enzyme. Hepatitis virus infection [1E50-1E51] [16]
Telaprevir DMMRV29 Major Decreased metabolism of Tamsulosin caused by Telaprevir mediated inhibition of CYP450 enzyme. Hepatitis virus infection [1E50-1E51] [16]
Procarbazine DMIK367 Moderate Additive hypotensive effects by the combination of Tamsulosin and Procarbazine. Hodgkin lymphoma [2B30] [19]
Fosamprenavir DM4W9B3 Major Decreased metabolism of Tamsulosin caused by Fosamprenavir mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [16]
Cobicistat DM6L4H2 Major Decreased metabolism of Tamsulosin caused by Cobicistat mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [16]
Saquinavir DMG814N Major Decreased metabolism of Tamsulosin caused by Saquinavir mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [16]
Darunavir DMN3GCH Moderate Decreased metabolism of Tamsulosin caused by Darunavir mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [15]
Atazanavir DMSYRBX Major Decreased metabolism of Tamsulosin caused by Atazanavir mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [16]
Cinacalcet DMCX0K3 Moderate Decreased metabolism of Tamsulosin caused by Cinacalcet mediated inhibition of CYP450 enzyme. Hyper-parathyroidism [5A51] [15]
Conivaptan DM1V329 Major Decreased metabolism of Tamsulosin caused by Conivaptan mediated inhibition of CYP450 enzyme. Hypo-osmolality/hyponatraemia [5C72] [16]
Givosiran DM5PFIJ Moderate Decreased metabolism of Tamsulosin caused by Givosiran mediated inhibition of CYP450 enzyme. Inborn porphyrin/heme metabolism error [5C58] [15]
Berotralstat DMWA2DZ Moderate Decreased metabolism of Tamsulosin caused by Berotralstat mediated inhibition of CYP450 enzyme. Innate/adaptive immunodeficiency [4A00] [22]
Propiomazine DMKY8V1 Moderate Additive hypotensive effects by the combination of Tamsulosin and Propiomazine. Insomnia [7A00-7A0Z] [17]
ITI-007 DMUQ1DO Moderate Additive hypotensive effects by the combination of Tamsulosin and ITI-007. Insomnia [7A00-7A0Z] [17]
Glycerol phenylbutyrate DMDGRQO Moderate Decreased metabolism of Tamsulosin caused by Glycerol phenylbutyrate mediated inhibition of CYP450 enzyme. Liver disease [DB90-DB9Z] [14]
Crizotinib DM4F29C Moderate Decreased metabolism of Tamsulosin caused by Crizotinib mediated inhibition of CYP450 enzyme. Lung cancer [2C25] [15]
Ceritinib DMB920Z Major Decreased metabolism of Tamsulosin caused by Ceritinib mediated inhibition of CYP450 enzyme. Lung cancer [2C25] [16]
PF-06463922 DMKM7EW Moderate Increased metabolism of Tamsulosin caused by PF-06463922 mediated induction of CYP450 enzyme. Lung cancer [2C25] [23]
Dacomitinib DMOH8VY Moderate Decreased metabolism of Tamsulosin caused by Dacomitinib mediated inhibition of CYP450 enzyme. Lung cancer [2C25] [15]
Selpercatinib DMZR15V Moderate Decreased metabolism of Tamsulosin caused by Selpercatinib mediated inhibition of CYP450 enzyme. Lung cancer [2C25] [14]
Idelalisib DM602WT Major Decreased metabolism of Tamsulosin caused by Idelalisib mediated inhibition of CYP450 enzyme. Mature B-cell leukaemia [2A82] [16]
IPI-145 DMWA24P Moderate Decreased metabolism of Tamsulosin caused by IPI-145 mediated inhibition of CYP450 enzyme. Mature B-cell leukaemia [2A82] [15]
Dabrafenib DMX6OE3 Moderate Increased metabolism of Tamsulosin caused by Dabrafenib mediated induction of CYP450 enzyme. Melanoma [2C30] [14]
Panobinostat DM58WKG Moderate Decreased metabolism of Tamsulosin caused by Panobinostat mediated inhibition of CYP450 enzyme. Multiple myeloma [2A83] [15]
Ozanimod DMT6AM2 Moderate Additive hypotensive effects by the combination of Tamsulosin and Ozanimod. Multiple sclerosis [8A40] [19]
Fedratinib DM4ZBK6 Moderate Decreased metabolism of Tamsulosin caused by Fedratinib mediated inhibition of CYP450 enzyme. Myeloproliferative neoplasm [2A20] [15]
Promethazine DM6I5GR Moderate Additive hypotensive effects by the combination of Tamsulosin and Promethazine. Nausea/vomiting [MD90] [17]
Rolapitant DM8XP26 Moderate Decreased metabolism of Tamsulosin caused by Rolapitant mediated inhibition of CYP450 enzyme. Nausea/vomiting [MD90] [15]
Netupitant DMEKAYI Moderate Decreased metabolism of Tamsulosin caused by Netupitant mediated inhibition of CYP450 enzyme. Nausea/vomiting [MD90] [15]
Bupropion DM5PCS7 Moderate Decreased metabolism of Tamsulosin caused by Bupropion mediated inhibition of CYP450 enzyme. Nicotine use disorder [6C4A] [15]
Lorcaserin DMG6OYJ Moderate Decreased metabolism of Tamsulosin caused by Lorcaserin mediated inhibition of CYP450 enzyme. Obesity [5B80-5B81] [15]
Dexfenfluramine DMJ7YDS Moderate Decreased metabolism of Tamsulosin caused by Dexfenfluramine mediated inhibition of CYP450 enzyme. Obesity [5B80-5B81] [15]
Rucaparib DM9PVX8 Moderate Decreased metabolism of Tamsulosin caused by Rucaparib mediated inhibition of CYP450 enzyme. Ovarian cancer [2C73] [24]
Safinamide DM0YWJC Moderate Additive hypotensive effects by the combination of Tamsulosin and Safinamide. Parkinsonism [8A00] [19]
Rasagiline DM3WKQ4 Moderate Additive hypotensive effects by the combination of Tamsulosin and Rasagiline. Parkinsonism [8A00] [19]
Abametapir DM2RX0I Moderate Decreased metabolism of Tamsulosin caused by Abametapir mediated inhibition of CYP450 enzyme. Pediculosis [1G00] [25]
Lefamulin DME6G97 Moderate Decreased metabolism of Tamsulosin caused by Lefamulin mediated inhibition of CYP450 enzyme. Pneumonia [CA40] [26]
Lonafarnib DMGM2Z6 Major Decreased metabolism of Tamsulosin caused by Lonafarnib mediated inhibition of CYP450 enzyme. Premature ageing appearance [LD2B] [16]
ABIRATERONE DM8V75C Moderate Decreased metabolism of Tamsulosin caused by ABIRATERONE mediated inhibition of CYP450 enzyme. Prostate cancer [2C82] [15]
Enzalutamide DMGL19D Moderate Increased metabolism of Tamsulosin caused by Enzalutamide mediated induction of CYP450 enzyme. Prostate cancer [2C82] [27]
Tolazoline DMI40NL Moderate Additive hypotensive effects by the combination of Tamsulosin and Tolazoline. Pulmonary hypertension [BB01] [13]
Mesoridazine DM2ZGAN Moderate Additive hypotensive effects by the combination of Tamsulosin and Mesoridazine. Schizophrenia [6A20] [17]
Aripiprazole DM3NUMH Moderate Additive hypotensive effects by the combination of Tamsulosin and Aripiprazole. Schizophrenia [6A20] [17]
Iloperidone DM6AUFY Moderate Additive hypotensive effects by the combination of Tamsulosin and Iloperidone. Schizophrenia [6A20] [17]
Perphenazine DMA4MRX Moderate Additive hypotensive effects by the combination of Tamsulosin and Perphenazine. Schizophrenia [6A20] [17]
Molindone DMAH70G Moderate Additive hypotensive effects by the combination of Tamsulosin and Molindone. Schizophrenia [6A20] [17]
Thiothixene DMDINC4 Moderate Additive hypotensive effects by the combination of Tamsulosin and Thiothixene. Schizophrenia [6A20] [17]
Trifluoperazine DMKBYWI Moderate Additive hypotensive effects by the combination of Tamsulosin and Trifluoperazine. Schizophrenia [6A20] [17]
Amisulpride DMSJVAM Moderate Additive hypotensive effects by the combination of Tamsulosin and Amisulpride. Schizophrenia [6A20] [17]
Voxelotor DMCS6M5 Moderate Decreased metabolism of Tamsulosin caused by Voxelotor mediated inhibition of CYP450 enzyme. Sickle-cell disorder [3A51] [15]
Telotristat ethyl DMDIYFZ Moderate Increased metabolism of Tamsulosin caused by Telotristat ethyl mediated induction of CYP450 enzyme. Small intestine developmental anomaly [DA90] [14]
Larotrectinib DM26CQR Moderate Decreased metabolism of Tamsulosin caused by Larotrectinib mediated inhibition of CYP450 enzyme. Solid tumour/cancer [2A00-2F9Z] [16]
LEE011 DMMX75K Moderate Decreased metabolism of Tamsulosin caused by LEE011 mediated inhibition of CYP450 enzyme. Solid tumour/cancer [2A00-2F9Z] [15]
Fostamatinib DM6AUHV Moderate Decreased metabolism of Tamsulosin caused by Fostamatinib mediated inhibition of CYP450 enzyme. Thrombocytopenia [3B64] [28]
Methdilazine DMAUHQX Moderate Additive hypotensive effects by the combination of Tamsulosin and Methdilazine. Vasomotor/allergic rhinitis [CA08] [17]
Trimeprazine DMEMV9D Moderate Additive hypotensive effects by the combination of Tamsulosin and Trimeprazine. Vasomotor/allergic rhinitis [CA08] [29]
Propafenone DMPIBJK Moderate Decreased metabolism of Tamsulosin caused by Propafenone mediated inhibition of CYP450 enzyme. Ventricular tachyarrhythmia [BC71] [15]
Amiodarone DMUTEX3 Moderate Decreased metabolism of Tamsulosin caused by Amiodarone mediated inhibition of CYP450 enzyme. Ventricular tachyarrhythmia [BC71] [15]
⏷ Show the Full List of 85 DDI Information of This Drug

Drug Inactive Ingredient(s) (DIG) and Formulation(s) of This Drug

DIG
DIG Name DIG ID PubChem CID Functional Classification
Allura red AC dye E00338 33258 Colorant
D&C red no. 28 E00491 6097185 Colorant
FD&C blue no. 1 E00263 19700 Colorant
FD&C blue no. 2 E00446 2723854 Colorant
Glyceryl monostearate E00310 24699 Emollient; Emulsifying agent; Emulsion stabilizing agent; Solubilizing agent; Surfactant; Viscosity-controlling agent
Isopropyl alcohol E00070 3776 Antimicrobial preservative; Solvent
Quinoline yellow WS E00309 24671 Colorant
Sodium lauryl sulfate E00464 3423265 Emulsifying agent; Modified-release agent; Penetration agent; Solubilizing agent; Surfactant; lubricant
Sunset yellow FCF E00255 17730 Colorant
Ammonia E00007 222 Alkalizing agent
Butyl alcohol E00011 263 Flavoring agent; Solvent
Calcium stearate E00244 15324 lubricant
Dibutyl sebacate E00160 7986 Plasticizing agent
Eisenoxyd E00585 56841934 Colorant
Ferric hydroxide oxide yellow E00539 23320441 Colorant
Ferrosoferric oxide E00231 14789 Colorant
Gelatin E00630 Not Available Other agent
Magnesium stearate E00208 11177 lubricant
Polyethylene glycol 6000 E00655 Not Available Coating agent; Diluent; Ointment base; Plasticizing agent; Solvent; Suppository base; lubricant
Polysorbate 80 E00665 Not Available Dispersing agent; Emollient; Emulsifying agent; Plasticizing agent; Solubilizing agent; Surfactant; Suspending agent
Potassium hydroxide E00233 14797 Alkalizing agent
Propylene glycol E00040 1030 Antimicrobial preservative; Humectant; Plasticizing agent; Solvent
Propylene glycol distearate E00395 110800 Emollient; Opacifying agent; Surfactant
Saccharose E00091 5988 Binding agent; Coating agent; Cryoprotectant; Diluent; Flavoring agent; Suspending agent; Viscosity-controlling agent
Silicon dioxide E00670 Not Available Anticaking agent; Opacifying agent; Viscosity-controlling agent
Sodium hydroxide E00234 14798 Alkalizing agent
Talc E00520 16211421 Anticaking agent; Diluent; Glidant; lubricant
Titanium dioxide E00322 26042 Coating agent; Colorant; Opacifying agent
Triacetin E00080 5541 Humectant; Plasticizing agent; Solvent
Triethyl citrate E00128 6506 Plasticizing agent; Solvent
Water E00035 962 Solvent
⏷ Show the Full List of 31 Pharmaceutical Excipients of This Drug
Pharmaceutical Formulation
Formulation Name Drug Dosage Dosage Form Route
Tamsulosin 0.4 mg capsule 0.4 mg Oral Capsule Oral
Jump to Detail Pharmaceutical Formulation Page of This Drug

References

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4 Critical Evaluation of Human Oral Bioavailability for Pharmaceutical Drugs by Using Various Cheminformatics Approaches
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6 Trend Analysis of a Database of Intravenous Pharmacokinetic Parameters in Humans for 1352 Drug Compounds
7 Greenblatt DJ, Wright CE: Clinical pharmacokinetics of alprazolam. Therapeutic implications. Clin Pharmacokinet. 1993 Jun;24(6):453-71. doi: 10.2165/00003088-199324060-00003.
8 Estimating the safe starting dose in phase I clinical trials and no observed effect level based on QSAR modeling of the human maximum recommended daily dose
9 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services.
10 Identification of cytochrome P450 isozymes involved in metabolism of the alpha1-adrenoceptor blocker tamsulosin in human liver microsomes. Xenobiotica. 1998 Oct;28(10):909-22.
11 Cell membrane chromatography competitive binding analysis for characterization of 1A adrenoreceptor binding interactions. Anal Bioanal Chem. 2011 Jul;400(10):3625-33. doi: 10.1007/s00216-011-5026-z. Epub 2011 May 5.
12 Evaluating the Role of Multidrug Resistance Protein 3 (MDR3) Inhibition in Predicting Drug-Induced Liver Injury Using 125 Pharmaceuticals. Chem Res Toxicol. 2017 May 15;30(5):1219-1229. doi: 10.1021/acs.chemrestox.7b00048. Epub 2017 May 4.
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