General Information of Drug (ID: DMJIBAW)

Drug Name
Budesonide
Synonyms
Bidien; Budenofalk; Budeson; Budesonido; Budesonidum; Budiair; Cortivent; Entocort; Horacort; Inflammide; Micronyl; Miflonide; Preferid; Pulmaxan; Respules; Rhinocort; Spirocort; UDB; Budecort Inhaler; Budesonide Easyhaler; Budesonide MMX; Entocort EC; GionaEasyhaler; Pulmaxan turbohaler; Pulmicort Flexhaler; Pulmicort Nebuamp; Pulmicort Respules; Pulmicort Topinasal; Pulmicort turbuhaler; Rhinocort Aqua; Rhinocort Turbuhaler; Rhinocort alpha; Unit dosebudesonide; B 7777; S 1320; Budesonido [INN-Spanish]; Budesonidum [INN-Latin]; Entocort (TN); Entocort EC (TN); MAP-0010; Noex (TN); Pulmicort (TN); Rhinocort (TN); S-1320; Budesonide (JAN/USAN/INN); Budesonide [USAN:INN:BAN:JAN]; Rhinocort, Pulmicort , Entocort, Symbicort, Noex. Entocort EC, Budesonide; Pregna-1,4-diene-3,20-dione, 16,17-butylidenebis(oxy)-11,21-dihydroxy-, (11beta,16alpha(R))-,and 16alpha,17-((S)-Butylidenebis(oxy))-11beta,21-dihydroxypregna-1,4-diene-3,20-dione; (11-beta,16-alpha)-16,17-(Butylidenebis(oxy))-11,21-dihydroxypregna-1,4-diene-3,20-dione; (11beta,16alpha)-16,17-(Butylidenebis(oxy))-11,21-dihydroxypregna-1,4-diene-3,20-dione; (4aR,4bS,5S,6aS,6bS,8R,9aR,10aS,10bS)-5-hydroxy-6b-(hydroxyacetyl)-4a,6a-dimethyl-8-propyl-4a,4b,5,6,6a,6b,9a,10,10a,10b,11,12-dodecahydro-2H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-2-one; (4aR,4bS,5S,6aS,6bS,9aR,10aS,10bS)-5-hydroxy-6b-(hydroxyacetyl)-4a,6a-dimethyl-8-propyl-4a,4b,5,6,6a,6b,9a,10,10a,10b,11,12-dodecahydro-2H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-2-one; (R,S)-11b,16a,17,21,tetrahydroxypregna-1,4-diene-3,20-dione cyclic 16,17-acetal with buty raldehyde; (RS)-(11beta,16alpha)-16,17-[Butylidenebis(oxy)]-11,21-dihydroxypregna-1,4-diene-3,20-dione; (RS)-11beta,16alpha,17,21-Tetrahydroxypregna-1,4-diene-3,20-dione cyclic 16,17-acetal with butyraldehyde; (S)-16alpha,17-(Butylidenedioxy)-11beta,21-dihydroxypregna-1,4-diene-3,20-dione; 11beta,21-dihydroxy-16alpha,17alpha-(butane-1,1-diyldioxy)pregna-1,4-diene-3,20-dione; 16,17-Butylidenebis(oxy)-11,21-dihydroxypregna-1,4-diene-3,20-dione; 16,17-Butylidenebis(oxy)-11-,21-dihydroxypregna-1,4-diene-3,20-dione; 16-alpha,17-alpha-Butylidenedioxy-11-beta,21-dihydroxy-1,4-pregnadiene-3,20-dione; 16alpha(R),17-(Butylidenebis(oxy))-11beta,21-dihydroxypregna-1,4-diene-3,20-dione; 16alpha-,17alpha-butylidenedioxypregna-1,4-diene-11beta-,21-diol-3,20-dione
Indication
Disease Entry ICD 11 Status REF
Allergic rhinitis CA08.0 Approved [1]
Asthma CA23 Approved [2]
Crohn disease DD70 Approved [1]
Inflammatory bowel disease DD72 Approved [1]
Radiation proctitis N.A. Approved [1]
Ulcerative colitis DD71 Approved [1]
Coronavirus Disease 2019 (COVID-19) 1D6Y Phase 3 [3]
⏷ Show the Full List of Indication(s)
Therapeutic Class
Antiinflammatory Agents
Drug Type
Small molecular drug
Structure
3D MOL 2D MOL
#Ro5 Violations (Lipinski): 0 Molecular Weight (mw) 430.5
Logarithm of the Partition Coefficient (xlogp) 2.5
Rotatable Bond Count (rotbonds) 4
Hydrogen Bond Donor Count (hbonddonor) 2
Hydrogen Bond Acceptor Count (hbondacc) 6
ADMET Property
BDDCS Class
Biopharmaceutics Drug Disposition Classification System (BDDCS) Class 1: high solubility and high permeability [4]
Clearance
The drug present in the plasma can be removed from the body at the rate of 20 mL/min/kg [5]
Elimination
0% of drug is excreted from urine in the unchanged form [4]
Half-life
The concentration or amount of drug in body reduced by one-half in 2.8 hours [5]
MRTD
The Maximum Recommended Therapeutic Dose (MRTD) of drug that ensured maximising efficacy and moderate side effect is 0.03964 micromolar/kg/day [6]
Unbound Fraction
The unbound fraction of drug in plasma is 0.13% [5]
Vd
Fluid volume that would be required to contain the amount of drug present in the body at the same concentration as in the plasma 3.9 L/kg [5]
Water Solubility
The ability of drug to dissolve in water is measured as 0.02 mg/mL [4]
Chemical Identifiers
Formula
C25H34O6
IUPAC Name
(1S,2S,4R,8S,9S,11S,12S,13R)-11-hydroxy-8-(2-hydroxyacetyl)-9,13-dimethyl-6-propyl-5,7-dioxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-14,17-dien-16-one
Canonical SMILES
CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@@]5([C@H]4[C@H](C[C@@]3([C@@]2(O1)C(=O)CO)C)O)C
InChI
InChI=1S/C25H34O6/c1-4-5-21-30-20-11-17-16-7-6-14-10-15(27)8-9-23(14,2)22(16)18(28)12-24(17,3)25(20,31-21)19(29)13-26/h8-10,16-18,20-22,26,28H,4-7,11-13H2,1-3H3/t16-,17-,18-,20+,21?,22+,23-,24-,25+/m0/s1
InChIKey
VOVIALXJUBGFJZ-KWVAZRHASA-N
Cross-matching ID
PubChem CID
5281004
ChEBI ID
CHEBI:3207
CAS Number
51333-22-3
DrugBank ID
DB01222
TTD ID
D0Y7IU
VARIDT ID
DR00323
INTEDE ID
DR0239
ACDINA ID
D00080
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
Glucocorticoid receptor (NR3C1) TTYRL6O GCR_HUMAN Antagonist [7]

Drug-Metabolizing Enzyme (DME)
DME Name DME ID UniProt ID MOA REF
Cytochrome P450 3A4 (CYP3A4) DE4LYSA CP3A4_HUMAN Substrate [8]
Sulfotransferase 1A1 (SULT1A1) DEYWLRK ST1A1_HUMAN Substrate [9]

Drug Off-Target (DOT)
DOT Name DOT ID UniProt ID Interaction REF
Apoptosis regulator Bcl-2 (BCL2) OT9DVHC0 BCL2_HUMAN Gene/Protein Processing [10]
ATP-dependent translocase ABCB1 (ABCB1) OTEJROBO MDR1_HUMAN Gene/Protein Processing [11]
Bile salt export pump (ABCB11) OTRU7THO ABCBB_HUMAN Gene/Protein Processing [12]
C-C motif chemokine 17 (CCL17) OTIKW21L CCL17_HUMAN Gene/Protein Processing [13]
C-C motif chemokine 2 (CCL2) OTAD2HEL CCL2_HUMAN Gene/Protein Processing [14]
C-C motif chemokine 3 (CCL3) OTW2H3ND CCL3_HUMAN Gene/Protein Processing [14]
C-C motif chemokine 4 (CCL4) OT6B8P25 CCL4_HUMAN Gene/Protein Processing [14]
Caspase-9 (CASP9) OTD4RFFG CASP9_HUMAN Gene/Protein Processing [15]
Cellular tumor antigen p53 (TP53) OTIE1VH3 P53_HUMAN Gene/Protein Processing [10]
Cytochrome P450 3A4 (CYP3A4) OTQGYY83 CP3A4_HUMAN Gene/Protein Processing [16]
Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This Drug

Molecular Expression Atlas of This Drug

The Studied Disease Allergic rhinitis
ICD Disease Classification CA08.0
Molecule Name Molecule Type Gene Name p-value Fold-Change Z-score
Glucocorticoid receptor (NR3C1) DTT NR3C1 7.57E-01 -0.04 -0.07
Sulfotransferase 1A1 (SULT1A1) DME SULT1A1 8.72E-02 6.46E-02 2.89E-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 Budesonide
DDI Drug Name DDI Drug ID Severity Mechanism Disease REF
Levalbuterol DM5YBO1 Minor Increased risk of hypokalemia by the combination of Budesonide and Levalbuterol. Asthma [CA23] [17]
Pirbuterol DMI5678 Minor Increased risk of hypokalemia by the combination of Budesonide and Pirbuterol. Asthma [CA23] [18]
Roflumilast DMPGHY8 Moderate Additive immunosuppressive effects by the combination of Budesonide and Roflumilast. Asthma [CA23] [19]
Coadministration of a Drug Treating the Disease Different from Budesonide (Comorbidity)
DDI Drug Name DDI Drug ID Severity Mechanism Comorbidity REF
Dronedarone DMA8FS5 Moderate Decreased metabolism of Budesonide caused by Dronedarone mediated inhibition of CYP450 enzyme. Angina pectoris [BA40] [20]
Posaconazole DMUL5EW Major Decreased metabolism of Budesonide caused by Posaconazole mediated inhibition of CYP450 enzyme. Aspergillosis [1F20] [20]
Dalfopristin DM4LTKV Moderate Decreased metabolism of Budesonide caused by Dalfopristin mediated inhibition of CYP450 enzyme. Bacterial infection [1A00-1C4Z] [20]
Troleandomycin DMUZNIG Major Decreased metabolism of Budesonide caused by Troleandomycin mediated inhibition of CYP450 enzyme. Bacterial infection [1A00-1C4Z] [20]
Pexidartinib DMS2J0Z Moderate Increased metabolism of Budesonide caused by Pexidartinib mediated induction of CYP450 enzyme. Bone/articular cartilage neoplasm [2F7B] [21]
Lapatinib DM3BH1Y Moderate Decreased metabolism of Budesonide caused by Lapatinib mediated inhibition of CYP450 enzyme. Breast cancer [2C60-2C6Y] [20]
Tucatinib DMBESUA Major Decreased metabolism of Budesonide caused by Tucatinib mediated inhibition of CYP450 enzyme. Breast cancer [2C60-2C6Y] [20]
Vilanterol DMF5EK1 Minor Increased risk of hypokalemia by the combination of Budesonide and Vilanterol. Chronic obstructive pulmonary disease [CA22] [17]
Indacaterol DMQJHR7 Minor Increased risk of hypokalemia by the combination of Budesonide and Indacaterol. Chronic obstructive pulmonary disease [CA22] [18]
Arformoterol DMYM974 Minor Increased risk of hypokalemia by the combination of Budesonide and Arformoterol. Chronic obstructive pulmonary disease [CA22] [18]
Osilodrostat DMIJC9X Moderate Decreased metabolism of Budesonide caused by Osilodrostat mediated inhibition of CYP450 enzyme. Cushing syndrome [5A70] [20]
Ivacaftor DMZC1HS Moderate Decreased metabolism of Budesonide caused by Ivacaftor mediated inhibition of CYP450 enzyme. Cystic fibrosis [CA25] [20]
MK-8228 DMOB58Q Moderate Decreased metabolism of Budesonide caused by MK-8228 mediated inhibition of CYP450 enzyme. Cytomegaloviral disease [1D82] [20]
Stiripentol DMMSDOY Moderate Decreased metabolism of Budesonide caused by Stiripentol mediated inhibition of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [20]
Boceprevir DMBSHMF Major Decreased metabolism of Budesonide caused by Boceprevir mediated inhibition of CYP450 enzyme. Hepatitis virus infection [1E50-1E51] [20]
Telaprevir DMMRV29 Major Decreased metabolism of Budesonide caused by Telaprevir mediated inhibition of CYP450 enzyme. Hepatitis virus infection [1E50-1E51] [20]
Fosamprenavir DM4W9B3 Major Decreased metabolism of Budesonide caused by Fosamprenavir mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [20]
Cobicistat DM6L4H2 Major Decreased metabolism of Budesonide caused by Cobicistat mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [20]
Saquinavir DMG814N Major Decreased metabolism of Budesonide caused by Saquinavir mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [20]
Darunavir DMN3GCH Moderate Decreased metabolism of Budesonide caused by Darunavir mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [20]
Bempedoic acid DM1CI9R Major Increased risk of tendinitis/tendon rupture by the combination of Budesonide and Bempedoic acid. Hyper-lipoproteinaemia [5C80] [22]
Teriflunomide DMQ2FKJ Major Additive immunosuppressive effects by the combination of Budesonide and Teriflunomide. Hyper-lipoproteinaemia [5C80] [23]
BMS-201038 DMQTAGO Moderate Decreased metabolism of Budesonide caused by BMS-201038 mediated inhibition of CYP450 enzyme. Hyper-lipoproteinaemia [5C80] [20]
Berotralstat DMWA2DZ Moderate Decreased metabolism of Budesonide caused by Berotralstat mediated inhibition of CYP450 enzyme. Innate/adaptive immunodeficiency [4A00] [20]
Denosumab DMNI0KO Moderate Additive immunosuppressive effects by the combination of Budesonide and Denosumab. Low bone mass disorder [FB83] [24]
Crizotinib DM4F29C Moderate Decreased metabolism of Budesonide caused by Crizotinib mediated inhibition of CYP450 enzyme. Lung cancer [2C25] [20]
Ceritinib DMB920Z Major Decreased metabolism of Budesonide caused by Ceritinib mediated inhibition of CYP450 enzyme. Lung cancer [2C25] [20]
Selpercatinib DMZR15V Moderate Decreased metabolism of Budesonide caused by Selpercatinib mediated inhibition of CYP450 enzyme. Lung cancer [2C25] [20]
Idelalisib DM602WT Major Decreased metabolism of Budesonide caused by Idelalisib mediated inhibition of CYP450 enzyme. Mature B-cell leukaemia [2A82] [20]
IPI-145 DMWA24P Moderate Decreased metabolism of Budesonide caused by IPI-145 mediated inhibition of CYP450 enzyme. Mature B-cell leukaemia [2A82] [20]
Nivolumab DMAB9QE Moderate Additive immunosuppressive effects by the combination of Budesonide and Nivolumab. Melanoma [2C30] [18]
Pembrolizumab DMFQEA6 Moderate Additive immunosuppressive effects by the combination of Budesonide and Pembrolizumab. Melanoma [2C30] [18]
Ipilimumab DMJTIYK Moderate Additive immunosuppressive effects by the combination of Budesonide and Ipilimumab. Melanoma [2C30] [18]
Cemiplimab DMKMJHE Moderate Additive immunosuppressive effects by the combination of Budesonide and Cemiplimab. Melanoma [2C30] [18]
Danazol DML8KTN Moderate Decreased metabolism of Budesonide caused by Danazol mediated inhibition of CYP450 enzyme. Menstrual cycle bleeding disorder [GA20] [20]
Tecfidera DM2OVDT Moderate Additive immunosuppressive effects by the combination of Budesonide and Tecfidera. Multiple sclerosis [8A40] [25]
Siponimod DM2R86O Major Additive immunosuppressive effects by the combination of Budesonide and Siponimod. Multiple sclerosis [8A40] [17]
Fingolimod DM5JVAN Major Additive immunosuppressive effects by the combination of Budesonide and Fingolimod. Multiple sclerosis [8A40] [26]
Ocrelizumab DMEZ2KH Moderate Additive immunosuppressive effects by the combination of Budesonide and Ocrelizumab. Multiple sclerosis [8A40] [27]
Ozanimod DMT6AM2 Major Additive immunosuppressive effects by the combination of Budesonide and Ozanimod. Multiple sclerosis [8A40] [19]
Fedratinib DM4ZBK6 Moderate Decreased metabolism of Budesonide caused by Fedratinib mediated inhibition of CYP450 enzyme. Myeloproliferative neoplasm [2A20] [20]
Nilotinib DM7HXWT Moderate Decreased metabolism of Budesonide caused by Nilotinib mediated inhibition of CYP450 enzyme. Myeloproliferative neoplasm [2A20] [20]
Dasatinib DMJV2EK Moderate Decreased metabolism of Budesonide caused by Dasatinib mediated inhibition of CYP450 enzyme. Myeloproliferative neoplasm [2A20] [20]
Omacetaxine mepesuccinate DMPU2WX Moderate Additive immunosuppressive effects by the combination of Budesonide and Omacetaxine mepesuccinate. Myeloproliferative neoplasm [2A20] [28]
Netupitant DMEKAYI Moderate Decreased metabolism of Budesonide caused by Netupitant mediated inhibition of CYP450 enzyme. Nausea/vomiting [MD90] [20]
Atezolizumab DMMF8U0 Moderate Additive immunosuppressive effects by the combination of Budesonide and Atezolizumab. Non-small cell lung cancer [2C25] [18]
Entrectinib DMMPTLH Moderate Decreased metabolism of Budesonide caused by Entrectinib mediated inhibition of CYP450 enzyme. Non-small cell lung cancer [2C25] [20]
Rucaparib DM9PVX8 Moderate Decreased metabolism of Budesonide caused by Rucaparib mediated inhibition of CYP450 enzyme. Ovarian cancer [2C73] [20]
Abametapir DM2RX0I Moderate Decreased metabolism of Budesonide caused by Abametapir mediated inhibition of CYP450 enzyme. Pediculosis [1G00] [29]
Lefamulin DME6G97 Moderate Decreased metabolism of Budesonide caused by Lefamulin mediated inhibition of CYP450 enzyme. Pneumonia [CA40] [30]
Choline salicylate DM8P137 Moderate Increased risk of GI mucosal injury/bleeding risk by the combination of Budesonide and Choline salicylate. Postoperative inflammation [1A00-CA43] [31]
Lonafarnib DMGM2Z6 Major Decreased metabolism of Budesonide caused by Lonafarnib mediated inhibition of CYP450 enzyme. Premature ageing appearance [LD2B] [20]
Temsirolimus DMS104F Moderate Increased plasma concentrations of Budesonide and Temsirolimus due to competitive inhibition of the same metabolic pathway. Renal cell carcinoma [2C90] [32]
Salsalate DM13P4C Moderate Increased risk of GI mucosal injury/bleeding risk by the combination of Budesonide and Salsalate. Rheumatoid arthritis [FA20] [31]
Canakinumab DM8HLO5 Moderate Additive immunosuppressive effects by the combination of Budesonide and Canakinumab. Rheumatoid arthritis [FA20] [33]
Rilonacept DMGLUQS Moderate Additive immunosuppressive effects by the combination of Budesonide and Rilonacept. Rheumatoid arthritis [FA20] [33]
Golimumab DMHZV7X Major Additive immunosuppressive effects by the combination of Budesonide and Golimumab. Rheumatoid arthritis [FA20] [34]
Anthrax vaccine DM9GSWY Moderate Antagonize the effect of Budesonide when combined with Anthrax vaccine. Sepsis [1G40-1G41] [35]
Voxelotor DMCS6M5 Moderate Decreased metabolism of Budesonide caused by Voxelotor mediated inhibition of CYP450 enzyme. Sickle-cell disorder [3A51] [20]
Larotrectinib DM26CQR Moderate Decreased metabolism of Budesonide caused by Larotrectinib mediated inhibition of CYP450 enzyme. Solid tumour/cancer [2A00-2F9Z] [20]
LEE011 DMMX75K Moderate Decreased metabolism of Budesonide caused by LEE011 mediated inhibition of CYP450 enzyme. Solid tumour/cancer [2A00-2F9Z] [20]
Pitolisant DM8RFNJ Moderate Increased risk of GI mucosal injury/bleeding risk by the combination of Budesonide and Pitolisant. Somnolence [MG42] [19]
Fostamatinib DM6AUHV Moderate Decreased metabolism of Budesonide caused by Fostamatinib mediated inhibition of CYP450 enzyme. Thrombocytopenia [3B64] [36]
Brilinta DMBR01X Moderate Decreased metabolism of Budesonide caused by Brilinta mediated inhibition of CYP450 enzyme. Thrombosis [DB61-GB90] [20]
Durvalumab DM4PVDY Moderate Additive immunosuppressive effects by the combination of Budesonide and Durvalumab. Ureteral cancer [2C92] [18]
⏷ Show the Full List of 65 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
Acetic acid E00002 176 Acidulant; Buffering agent
Allura red AC dye E00338 33258 Colorant
Cetyl alcohol E00061 2682 Coating agent; Emollient; Emulsifying agent; Stiffening agent
D&C red no. 28 E00491 6097185 Colorant
D&C red no. 33 E00261 19116 Colorant
Ethyl acrylate E00191 8821 Film/membrane-forming agent; Flavoring agent
FD&C blue no. 1 E00263 19700 Colorant
FD&C blue no. 2 E00446 2723854 Colorant
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
Stearic acid E00079 5281 Emulsifying agent; Solubilizing agent; Viscosity-controlling agent; lubricant
Sunset yellow FCF E00255 17730 Colorant
Acetyltributyl citrate E00127 6505 Plasticizing agent
Ammonia E00007 222 Alkalizing agent
Beta-D-lactose E00099 6134 Diluent; Dry powder inhaler carrier; Lyophilization aid
Butyl alcohol E00011 263 Flavoring agent; Solvent
Crospovidone E00626 Not Available Disintegrant
Eisenoxyd E00585 56841934 Colorant
Ferric hydroxide oxide yellow E00539 23320441 Colorant
Ferrosoferric oxide E00231 14789 Colorant
Hydroxypropyl cellulose E00632 Not Available Binding agent; Coating agent; Emulsifying agent; Film/Membrane-forming agent; Modified-release agent; Suspending agent; Viscosity-controlling agent
Lactose monohydrate E00393 104938 Binding agent; Diluent; Dry powder inhaler carrier; Lyophilization aid
Magnesium stearate E00208 11177 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
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
Soybean lecithin E00637 Not Available Other agent
Talc E00520 16211421 Anticaking agent; Diluent; Glidant; lubricant
Titanium dioxide E00322 26042 Coating agent; Colorant; Opacifying agent
Triethyl citrate E00128 6506 Plasticizing agent; Solvent
Water E00035 962 Solvent
⏷ Show the Full List of 35 Pharmaceutical Excipients of This Drug
Pharmaceutical Formulation
Formulation Name Drug Dosage Dosage Form Route
Budesonide 3 mg capsule 3 mg Delayed Release Oral Capsule Oral
Budesonide 9 mg tablet 9 mg 24 HR Extended Release Oral Tablet Oral
Jump to Detail Pharmaceutical Formulation Page of This Drug

References

1 Budesonide FDA Label
2 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 7434).
3 Inhaled Corticosteroid Treatment of COVID19 Patients With Pneumonia
4 BDDCS applied to over 900 drugs
5 Trend Analysis of a Database of Intravenous Pharmacokinetic Parameters in Humans for 1352 Drug Compounds
6 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
7 PXR-mediated induction of human CYP3A4 and mouse Cyp3a11 by the glucocorticoid budesonide. Eur J Pharm Sci. 2009 Mar 2;36(4-5):565-71.
8 No relevant effect of ursodeoxycholic acid on cytochrome P450 3A metabolism in primary biliary cirrhosis. Hepatology. 2005 Mar;41(3):595-602.
9 Sulfation of budesonide by human cytosolic sulfotransferase, dehydroepiandrosterone-sulfotransferase (DHEA-ST). Drug Metab Dispos. 2002 May;30(5):582-5.
10 A randomized phase IIb trial of pulmicort turbuhaler (budesonide) in people with dysplasia of the bronchial epithelium. Clin Cancer Res. 2004 Oct 1;10(19):6502-11. doi: 10.1158/1078-0432.CCR-04-0686.
11 Oral and inhaled corticosteroids: differences in P-glycoprotein (ABCB1) mediated efflux. Toxicol Appl Pharmacol. 2012 May 1;260(3):294-302. doi: 10.1016/j.taap.2012.03.008. Epub 2012 Mar 23.
12 Early identification of clinically relevant drug interactions with the human bile salt export pump (BSEP/ABCB11). Toxicol Sci. 2013 Dec;136(2):328-43.
13 Effect of inhaled corticosteroid on an immunoreactive thymus and activation-regulated chemokine expression in the bronchial biopsies from asthmatics. Allergy. 2005 Mar;60(3):317-22. doi: 10.1111/j.1398-9995.2005.00694.x.
14 Cell-based and cytokine-directed chemical screen to identify potential anti-multiple myeloma agents. Leuk Res. 2010 Jul;34(7):917-24. doi: 10.1016/j.leukres.2009.12.002. Epub 2010 Feb 8.
15 Apoptosis of airway epithelial cells induced by corticosteroids. Am J Respir Crit Care Med. 2001 Nov 15;164(10 Pt 1):1939-47. doi: 10.1164/ajrccm.164.10.2103013.
16 Expression and regulation of the bile acid transporter, OSTalpha-OSTbeta in rat and human intestine and liver. Biopharm Drug Dispos. 2009 Jul;30(5):241-58.
17 Cerner Multum, Inc. "Australian Product Information.".
18 Agencia Espaola de Medicamentos y Productos Sanitarios Healthcare "Centro de informacion online de medicamentos de la AEMPS - CIMA.".
19 Cerner Multum, Inc. "UK Summary of Product Characteristics.".
20 Bolland MJ, Bagg W, Thomas MG, Lucas JA, Ticehurst R, Black PN "Cushing's syndrome due to interaction between inhaled corticosteroids and itraconazole." Ann Pharmacother 38 (2004): 46-9. [PMID: 14742792]
21 Product Information. Turalio (pexidartinib). Daiichi Sankyo, Inc., Parsippany, NJ.
22 Product Information. Nexletol (bempedoic acid). Esperion Therapeutics, Ann Arbor, MI.
23 Product Information. Arava (leflunomide). Hoechst Marion-Roussel Inc, Kansas City, MO.
24 Product Information. Prolia (denosumab). Amgen USA, Thousand Oaks, CA.
25 Product Information. Vumerity (diroximel fumarate). Alkermes, Inc, Cambridge, MA.
26 Product Information. Gilenya (fingolimod). Novartis Pharmaceuticals, East Hanover, NJ.
27 Product Information. Ocrevus (ocrelizumab). Genentech, South San Francisco, CA.
28 Product Information. Synribo (omacetaxine). Teva Pharmaceuticals USA, North Wales, PA.
29 Product Information. Xeglyze (abametapir topical). Dr. Reddy's Laboratories Inc, Upper Saddle River, NJ.
30 Product Information. Xenleta (lefamulin). Nabriva Therapeutics US, Inc., King of Prussia, PA.
31 Baer PA, Shore A, Ikeman RL "Transient fall in serum salicylate levels following intraarticular injection of steroid in patients with rheumatoid arthritis." Arthritis Rheum 30 (1987): 345-7. [PMID: 3566826]
32 Product Information. Prograf (tacrolimus). Fujisawa, Deerfield, IL.
33 Product Information. Arcalyst (rilonacept). Regeneron Pharmaceuticals Inc, Tarrytown, NY.
34 Product Information. Cimzia (certolizumab). UCB Pharma Inc, Smyrna, GA.
35 CDC. Centers for Disease Control and Prevention/ "Recommendations of the advisory committtee on immunization practices (ACIP): use of vaccines and immune globulins in persons with altered immunocompetence." MMWR Morb Mortal Wkly Rep 42(RR-04) (1993): 1-18. [PMID: 20300058]
36 Product Information. Tavalisse (fostamatinib). Rigel Pharmaceuticals, South San Francisco, CA.