General Information of Drug (ID: DMZ7XNQ)

Drug Name
Tacrolimus
Synonyms
Advagraf; Fujimycin; Graceptor; Modigraf; Prograf; Protopic; Protopy; Tacarolimus; Tsukubaenolide; Tacrolimus anhydrous; FK 506; FK5; FK506; FR 900506; FR900506; K506; L 679934; Advagraf (TN); FR-900506; Fk-506; L-679934; LCP-Tacro; Prograf (TN); Protopic (TN); Tacrolimus (INN); Tacrolimus (Prograf); Tacrolimus (anhydrous); (-)-FK 506; 15,19-epoxy-3H-pyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21(23H)-tetrone; 8-DEETHYL-8-[BUT-3-ENYL]-ASCOMYCIN
Indication
Disease Entry ICD 11 Status REF
Graft-versus-host disease 4B24 Approved [1]
Hepatosplenic T-cell lymphoma N.A. Approved [1]
Kidney transplant rejection NE84 Approved [1]
Large granular lymphocytic leukemia 2A90.1 Approved [1]
Leukemia N.A. Approved [1]
Lupus nephritis 4A40.0Y Approved [1]
MALT lymphoma N.A. Approved [1]
Myeloproliferative neoplasm 2A20 Approved [1]
Nodal marginal zone lymphoma 2A85.0 Approved [1]
Organ transplant rejection NE84 Approved [2]
Primary cutaneous peripheral T-cell lymphoma not otherwise specified N.A. Approved [1]
Recurrent adult burkitt lymphoma 2A85.6 Approved [1]
Small intestine lymphoma N.A. Approved [1]
Splenic marginal zone lymphoma N.A. Approved [1]
Testicular lymphoma N.A. Approved [1]
Ocular allergy 4A81 Phase 3 [2]
Classic Hodgkin lymphoma N.A. Investigative [1]
⏷ Show the Full List of Indication(s)
Therapeutic Class
Immunosuppressive Agents
Drug Type
Small molecular drug
Structure
3D MOL 2D MOL
#Ro5 Violations (Lipinski): 2 Molecular Weight (mw) 804
Logarithm of the Partition Coefficient (xlogp) 2.7
Rotatable Bond Count (rotbonds) 7
Hydrogen Bond Donor Count (hbonddonor) 3
Hydrogen Bond Acceptor Count (hbondacc) 12
ADMET Property
BDDCS Class
Biopharmaceutics Drug Disposition Classification System (BDDCS) Class 2: low solubility and high permeability [3]
Clearance
The drug present in the plasma can be removed from the body at the rate of 0.7 mL/min/kg [4]
Elimination
0.5% of drug is excreted from urine in the unchanged form [3]
Half-life
The concentration or amount of drug in body reduced by one-half in 35 hours (in adult healthy volunteers), 19 hours (in kidney transplant patients), 12 hours (in liver transplants patients), and 24 hours (in heart transplant patients) [4]
Metabolism
The drug is metabolized via the CYP3A4 and secondarily by CYP3A5 [5]
MRTD
The Maximum Recommended Therapeutic Dose (MRTD) of drug that ensured maximising efficacy and moderate side effect is 0.24329 micromolar/kg/day [6]
Unbound Fraction
The unbound fraction of drug in plasma is 0.01% [4]
Vd
The volume of distribution (Vd) of drug is 2.6 +/- 2.1 L/kg []
Water Solubility
The ability of drug to dissolve in water is measured as 0.008 mg/mL [3]
Adverse Drug Reaction (ADR)
ADR Term Variation Related DOT DOT ID REF
Nephropathy toxic Not Available PPP3R1 OTGQNFJQ [7]
Chemical Identifiers
Formula
C44H69NO12
IUPAC Name
(1R,9S,12S,13R,14S,17R,18E,21S,23S,24R,25S,27R)-1,14-dihydroxy-12-[(E)-1-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]prop-1-en-2-yl]-23,25-dimethoxy-13,19,21,27-tetramethyl-17-prop-2-enyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9]octacos-18-ene-2,3,10,16-tetrone
Canonical SMILES
C[C@@H]1C[C@@H]([C@@H]2[C@H](C[C@H]([C@@](O2)(C(=O)C(=O)N3CCCC[C@H]3C(=O)O[C@@H]([C@@H]([C@H](CC(=O)[C@@H](/C=C(/C1)\\C)CC=C)O)C)/C(=C/[C@@H]4CC[C@H]([C@@H](C4)OC)O)/C)O)C)OC)OC
InChI
InChI=1S/C44H69NO12/c1-10-13-31-19-25(2)18-26(3)20-37(54-8)40-38(55-9)22-28(5)44(52,57-40)41(49)42(50)45-17-12-11-14-32(45)43(51)56-39(29(6)34(47)24-35(31)48)27(4)21-30-15-16-33(46)36(23-30)53-7/h10,19,21,26,28-34,36-40,46-47,52H,1,11-18,20,22-24H2,2-9H3/b25-19+,27-21+/t26-,28+,29+,30-,31+,32-,33+,34-,36+,37-,38-,39+,40+,44+/m0/s1
InChIKey
QJJXYPPXXYFBGM-LFZNUXCKSA-N
Cross-matching ID
PubChem CID
445643
ChEBI ID
CHEBI:61049
CAS Number
104987-11-3
DrugBank ID
DB00864
TTD ID
D06OMK
VARIDT ID
DR00406
INTEDE ID
DR1524
ACDINA ID
D00648
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
Calcineurin (PPP3CA) TTA4LDE PP2BA_HUMAN Inhibitor [8]

Drug Transporter (DTP)
DTP Name DTP ID UniProt ID MOA REF
P-glycoprotein 1 (ABCB1) DTUGYRD MDR1_HUMAN Substrate [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 3A5 (CYP3A5) DEIBDNY CP3A5_HUMAN Substrate [11]
NADPH-cytochrome P450 reductase (CPR) DE3N2FM NCPR_HUMAN Substrate [12]
Ribosomal 23S RNA methyltransferase Erm (erm) DEW6V07 A0A5N1AHF6_CORAY Substrate [13]
Ribosomal 23S RNA methyltransferase Erm (erm) DEA65D8 A0A381KDL2_CORJE Substrate [13]

Drug Off-Target (DOT)
DOT Name DOT ID UniProt ID Interaction REF
Actin-related protein 2/3 complex subunit 5 (ARPC5) OTFNMMDL ARPC5_HUMAN Gene/Protein Processing [14]
Apoptosis regulator BAX (BAX) OTAW0V4V BAX_HUMAN Gene/Protein Processing [15]
ATP-dependent translocase ABCB1 (ABCB1) OTEJROBO MDR1_HUMAN Drug Response [16]
Baculoviral IAP repeat-containing protein 5 (BIRC5) OTILXZYL BIRC5_HUMAN Gene/Protein Processing [17]
Bile salt export pump (ABCB11) OTRU7THO ABCBB_HUMAN Gene/Protein Processing [18]
C-C chemokine receptor type 3 (CCR3) OT6GBUFA CCR3_HUMAN Gene/Protein Processing [19]
C-C motif chemokine 5 (CCL5) OTSCA5CK CCL5_HUMAN Gene/Protein Processing [19]
Cadherin-1 (CDH1) OTFJMXPM CADH1_HUMAN Gene/Protein Processing [20]
Calcineurin subunit B type 1 (PPP3R1) OTGQNFJQ CANB1_HUMAN Drug Response [7]
Caspase-3 (CASP3) OTIJRBE7 CASP3_HUMAN Protein Interaction/Cellular Processes [15]
Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This Drug

Molecular Expression Atlas of This Drug

The Studied Disease Graft-versus-host disease
ICD Disease Classification 4B24
Molecule Name Molecule Type Gene Name p-value Fold-Change Z-score
Calcineurin (PPP3CA) DTT PPP3CA 5.29E-01 1.74E-03 9.99E-03
P-glycoprotein 1 (ABCB1) DTP P-GP 2.00E-01 2.57E-02 6.18E-02
Cytochrome P450 3A5 (CYP3A5) DME CYP3A5 5.05E-02 4.52E-01 5.39E-01
Cytochrome P450 3A4 (CYP3A4) DME CYP3A4 8.67E-01 -3.83E-03 -1.24E-02
NADPH-cytochrome P450 reductase (CPR) DME POR 8.69E-02 -1.76E-01 -3.46E-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 Tacrolimus
DDI Drug Name DDI Drug ID Severity Mechanism Disease REF
Azathioprine DMMZSXQ Moderate Additive immunosuppressive effects by the combination of Tacrolimus and Azathioprine. Transplant rejection [NE84] [21]
Coadministration of a Drug Treating the Disease Different from Tacrolimus (Comorbidity)
DDI Drug Name DDI Drug ID Severity Mechanism Comorbidity REF
Remdesivir DMBFZ6L Moderate Decreased renal excretion of Tacrolimus caused by Remdesivir mediated nephrotoxicity. 1D6YCoronavirus Disease 2019 [1D6YCoronavirus Disease 2019] [21]
Sodium bicarbonate DMMU6BJ Moderate Decreased absorption of Tacrolimus due to altered gastric pH caused by Sodium bicarbonate. Acidosis [5C73] [22]
Repaglinide DM5SXUV Moderate Increased plasma concentrations of Tacrolimus and Repaglinide due to competitive inhibition of the same metabolic pathway. Acute diabete complication [5A2Y] [22]
Pioglitazone DMKJ485 Moderate Increased plasma concentrations of Tacrolimus and Pioglitazone due to competitive inhibition of the same metabolic pathway. Acute diabete complication [5A2Y] [22]
Ivosidenib DM8S6T7 Major Increased risk of prolong QT interval by the combination of Tacrolimus and Ivosidenib. Acute myeloid leukaemia [2A60] [23]
Midostaurin DMI6E0R Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Midostaurin. Acute myeloid leukaemia [2A60] [24]
Idarubicin DMM0XGL Moderate Decreased clearance of Tacrolimus due to the transporter inhibition by Idarubicin. Acute myeloid leukaemia [2A60] [25]
Arn-509 DMT81LZ Major Increased metabolism of Tacrolimus caused by Arn-509 mediated induction of CYP450 enzyme. Acute myeloid leukaemia [2A60] [26]
Gilteritinib DMTI0ZO Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Gilteritinib. Acute myeloid leukaemia [2A60] [27]
Oliceridine DM6MDCF Moderate Increased plasma concentrations of Tacrolimus and Oliceridine due to competitive inhibition of the same metabolic pathway. Acute pain [MG31] [22]
Framycetin DMF8DNE Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Framycetin. Alcoholic liver disease [DB94] [22]
Metronidazole DMTIVEN Moderate Decreased metabolism of Tacrolimus caused by Metronidazole mediated inhibition of CYP450 enzyme. Amoebiasis [1A36] [28]
Inotersen DMJ93CT Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Inotersen. Amyloidosis [5D00] [29]
Siltuximab DMGEATB Moderate Additive immunosuppressive effects by the combination of Tacrolimus and Siltuximab. Anemia [3A00-3A9Z] [29]
Ivabradine DM0L594 Major Increased risk of ventricular arrhythmias by the combination of Tacrolimus and Ivabradine. Angina pectoris [BA40] [29]
Bepridil DM0RKS4 Major Increased risk of prolong QT interval by the combination of Tacrolimus and Bepridil. Angina pectoris [BA40] [24]
Dronedarone DMA8FS5 Major Increased risk of prolong QT interval by the combination of Tacrolimus and Dronedarone. Angina pectoris [BA40] [24]
Nifedipine DMSVOZT Moderate Decreased metabolism of Tacrolimus caused by Nifedipine mediated inhibition of CYP450 enzyme. Angina pectoris [BA40] [30]
Bedaquiline DM3906J Major Increased risk of prolong QT interval by the combination of Tacrolimus and Bedaquiline. Antimicrobial drug resistance [MG50-MG52] [31]
Cilostazol DMZMSCT Moderate Increased plasma concentrations of Tacrolimus and Cilostazol due to competitive inhibition of the same metabolic pathway. Arterial occlusive disease [BD40] [22]
Posaconazole DMUL5EW Major Decreased metabolism of Tacrolimus caused by Posaconazole mediated inhibition of CYP450 enzyme. Aspergillosis [1F20] [32]
Levalbuterol DM5YBO1 Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Levalbuterol. Asthma [CA23] [33]
Terbutaline DMD4381 Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Terbutaline. Asthma [CA23] [34]
Pirbuterol DMI5678 Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Pirbuterol. Asthma [CA23] [34]
Budesonide DMJIBAW Moderate Increased plasma concentrations of Tacrolimus and Budesonide due to competitive inhibition of the same metabolic pathway. Asthma [CA23] [22]
Salbutamol DMN9CWF Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Salbutamol. Asthma [CA23] [33]
Roflumilast DMPGHY8 Moderate Additive immunosuppressive effects by the combination of Tacrolimus and Roflumilast. Asthma [CA23] [29]
Formoterol DMSOURV Moderate Increased risk of ventricular arrhythmias by the combination of Tacrolimus and Formoterol. Asthma [CA23] [34]
Lisdexamfetamine DM6W8V5 Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Lisdexamfetamine. Attention deficit hyperactivity disorder [6A05] [29]
Desipramine DMT2FDC Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Desipramine. Attention deficit hyperactivity disorder [6A05] [24]
Ofloxacin DM0VQN3 Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Ofloxacin. Bacterial infection [1A00-1C4Z] [35]
Kanamycin DM2DMPO Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Kanamycin. Bacterial infection [1A00-1C4Z] [22]
Tindamax DM3OWT4 Moderate Decreased metabolism of Tacrolimus caused by Tindamax mediated inhibition of CYP450 enzyme. Bacterial infection [1A00-1C4Z] [28]
Dalfopristin DM4LTKV Major Decreased metabolism of Tacrolimus caused by Dalfopristin mediated inhibition of CYP450 enzyme. Bacterial infection [1A00-1C4Z] [36]
Sulfamethoxazole DMB08GE Moderate Increased risk of nephrotoxicity by the combination of Tacrolimus and Sulfamethoxazole. Bacterial infection [1A00-1C4Z] [21]
Sparfloxacin DMB4HCT Major Increased risk of prolong QT interval by the combination of Tacrolimus and Sparfloxacin. Bacterial infection [1A00-1C4Z] [35]
Streptomycin DME1LQN Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Streptomycin. Bacterial infection [1A00-1C4Z] [22]
Gemifloxacin DMHT34O Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Gemifloxacin. Bacterial infection [1A00-1C4Z] [35]
Norfloxacin DMIZ6W2 Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Norfloxacin. Bacterial infection [1A00-1C4Z] [35]
Rabeprazole DMMZXIW Moderate Increased risk of hypomagnesemia by the combination of Tacrolimus and Rabeprazole. Bacterial infection [1A00-1C4Z] [37]
Netilmicin DMRD1QK Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Netilmicin. Bacterial infection [1A00-1C4Z] [22]
Levofloxacin DMS60RB Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Levofloxacin. Bacterial infection [1A00-1C4Z] [35]
Troleandomycin DMUZNIG Major Increased risk of prolong QT interval by the combination of Tacrolimus and Troleandomycin. Bacterial infection [1A00-1C4Z] [38]
Lomefloxacin DMVRH9C Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Lomefloxacin. Bacterial infection [1A00-1C4Z] [24]
Retigabine DMGNYIH Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Retigabine. Behcet disease [4A62] [24]
Erdafitinib DMI782S Moderate Increased metabolism of Tacrolimus caused by Erdafitinib mediated induction of CYP450 enzyme. Bladder cancer [2C94] [39]
Etidronic acid DM1XHYJ Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Etidronic acid. Bone paget disease [FB85] [22]
Pexidartinib DMS2J0Z Moderate Increased metabolism of Tacrolimus caused by Pexidartinib mediated induction of CYP450 enzyme. Bone/articular cartilage neoplasm [2F7B] [21]
Eribulin DM1DX4Q Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Eribulin. Breast cancer [2C60-2C6Y] [24]
Talazoparib DM1KS78 Moderate Decreased clearance of Tacrolimus due to the transporter inhibition by Talazoparib. Breast cancer [2C60-2C6Y] [40]
Lapatinib DM3BH1Y Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Lapatinib. Breast cancer [2C60-2C6Y] [24]
Exemestane DM9HPW3 Moderate Increased plasma concentrations of Tacrolimus and Exemestane due to competitive inhibition of the same metabolic pathway. Breast cancer [2C60-2C6Y] [22]
Tucatinib DMBESUA Major Decreased metabolism of Tacrolimus caused by Tucatinib mediated inhibition of CYP450 enzyme. Breast cancer [2C60-2C6Y] [32]
Palbociclib DMD7L94 Moderate Decreased metabolism of Tacrolimus caused by Palbociclib mediated inhibition of CYP450 enzyme. Breast cancer [2C60-2C6Y] [21]
Letrozole DMH07Y3 Moderate Increased plasma concentrations of Tacrolimus and Letrozole due to competitive inhibition of the same metabolic pathway. Breast cancer [2C60-2C6Y] [22]
Quinestrol DMJ6H1Z Moderate Increased plasma concentrations of Tacrolimus and Quinestrol due to competitive inhibition of the same metabolic pathway. Breast cancer [2C60-2C6Y] [22]
Cabazitaxel DMPAZHC Moderate Increased plasma concentrations of Tacrolimus and Cabazitaxel due to competitive inhibition of the same metabolic pathway. Breast cancer [2C60-2C6Y] [22]
Bosutinib DMTI8YE Moderate Decreased clearance of Tacrolimus due to the transporter inhibition by Bosutinib. Breast cancer [2C60-2C6Y] [29]
Atorvastatin DMF28YC Moderate Increased plasma concentrations of Tacrolimus and Atorvastatin due to competitive inhibition of the same metabolic pathway. Cardiovascular disease [BA00-BE2Z] [41]
Iodipamide DMXIQYS Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Iodipamide. Cholelithiasis [DC11] [42]
PF-04449913 DMSB068 Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and PF-04449913. Chronic myelomonocytic leukaemia [2A40] [43]
Olodaterol DM62B78 Moderate Increased risk of ventricular arrhythmias by the combination of Tacrolimus and Olodaterol. Chronic obstructive pulmonary disease [CA22] [34]
Vilanterol DMF5EK1 Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Vilanterol. Chronic obstructive pulmonary disease [CA22] [33]
Salmeterol DMIEU69 Moderate Increased risk of ventricular arrhythmias by the combination of Tacrolimus and Salmeterol. Chronic obstructive pulmonary disease [CA22] [34]
Indacaterol DMQJHR7 Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Indacaterol. Chronic obstructive pulmonary disease [CA22] [34]
Arformoterol DMYM974 Moderate Increased risk of ventricular arrhythmias by the combination of Tacrolimus and Arformoterol. Chronic obstructive pulmonary disease [CA22] [34]
Dihydrocodeine DMB0FWL Moderate Increased plasma concentrations of Tacrolimus and Dihydrocodeine due to competitive inhibition of the same metabolic pathway. Chronic pain [MG30] [22]
Ketoprofen DMRKXPT Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Ketoprofen. Chronic pain [MG30] [22]
Fidaxomicin DMFP6MV Minor Decreased clearance of Tacrolimus due to the transporter inhibition by Fidaxomicin. Clostridium difficile enterocolitis [1A04] [44]
Isoproterenol DMK7MEY Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Isoproterenol. Conduction disorder [BC63] [33]
Drospirenone DM1A9W3 Moderate Increased risk of hyperkalemia by the combination of Tacrolimus and Drospirenone. Contraceptive management [QA21] [45]
Levonorgestrel DM1DP7T Moderate Increased plasma concentrations of Tacrolimus and Levonorgestrel due to competitive inhibition of the same metabolic pathway. Contraceptive management [QA21] [22]
Levobupivacaine DM783CH Moderate Increased plasma concentrations of Tacrolimus and Levobupivacaine due to competitive inhibition of the same metabolic pathway. Corneal disease [9A76-9A78] [22]
Sevoflurane DMC9O43 Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Sevoflurane. Corneal disease [9A76-9A78] [24]
Methoxyflurane DML0RAE Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Methoxyflurane. Corneal disease [9A76-9A78] [22]
Cocaine DMSOX7I Moderate Increased plasma concentrations of Tacrolimus and Cocaine due to competitive inhibition of the same metabolic pathway. Corneal disease [9A76-9A78] [22]
Probucol DMVZQ2M Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Probucol. Coronary atherosclerosis [BA80] [24]
Pasireotide DMHM7JS Major Increased risk of prolong QT interval by the combination of Tacrolimus and Pasireotide. Cushing syndrome [5A70] [24]
Osilodrostat DMIJC9X Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Osilodrostat. Cushing syndrome [5A70] [29]
Lumacaftor DMCLWDJ Major Increased metabolism of Tacrolimus caused by Lumacaftor mediated induction of CYP450 enzyme. Cystic fibrosis [CA25] [21]
Ivacaftor DMZC1HS Moderate Decreased clearance of Tacrolimus due to the transporter inhibition by Ivacaftor. Cystic fibrosis [CA25] [46]
MK-8228 DMOB58Q Major Decreased metabolism of Tacrolimus caused by MK-8228 mediated inhibition of CYP450 enzyme. Cytomegaloviral disease [1D82] [47]
Rivaroxaban DMQMBZ1 Moderate Decreased metabolism of Tacrolimus caused by Rivaroxaban mediated inhibition of CYP450 enzyme. Deep vein thrombosis [BD71] [48]
Sertraline DM0FB1J Moderate Increased plasma concentrations of Tacrolimus and Sertraline due to competitive inhibition of the same metabolic pathway. Depression [6A70-6A7Z] [22]
Cyclobenzaprine DM1YBRM Moderate Increased plasma concentrations of Tacrolimus and Cyclobenzaprine due to competitive inhibition of the same metabolic pathway. Depression [6A70-6A7Z] [22]
Nefazodone DM4ZS8M Major Decreased metabolism of Tacrolimus caused by Nefazodone mediated inhibition of CYP450 enzyme. Depression [6A70-6A7Z] [32]
Escitalopram DMFK9HG Major Increased risk of prolong QT interval by the combination of Tacrolimus and Escitalopram. Depression [6A70-6A7Z] [24]
OPC-34712 DMHG57U Moderate Increased plasma concentrations of Tacrolimus and OPC-34712 due to competitive inhibition of the same metabolic pathway. Depression [6A70-6A7Z] [22]
Clomipramine DMINRKW Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Clomipramine. Depression [6A70-6A7Z] [24]
Doxepin DMPI98T Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Doxepin. Depression [6A70-6A7Z] [24]
Maprotiline DMPWB7T Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Maprotiline. Depression [6A70-6A7Z] [24]
Tetrabenazine DMYWQ0O Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Tetrabenazine. Dissociative neurological symptom disorder [6B60] [24]
Deutetrabenazine DMUPFLI Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Deutetrabenazine. Dystonic disorder [8A02] [49]
Ingrezza DMVPLNC Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Ingrezza. Dystonic disorder [8A02] [50]
Zonisamide DM0DTF7 Moderate Increased plasma concentrations of Tacrolimus and Zonisamide due to competitive inhibition of the same metabolic pathway. Epilepsy/seizure [8A61-8A6Z] [22]
Felbamate DM1V5ZS Moderate Increased metabolism of Tacrolimus caused by Felbamate mediated induction of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [21]
Cenobamate DM8KLU9 Moderate Increased metabolism of Tacrolimus caused by Cenobamate mediated induction of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [21]
Tiagabine DMKSQG0 Moderate Increased plasma concentrations of Tacrolimus and Tiagabine due to competitive inhibition of the same metabolic pathway. Epilepsy/seizure [8A61-8A6Z] [22]
Stiripentol DMMSDOY Moderate Decreased metabolism of Tacrolimus caused by Stiripentol mediated inhibition of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [51]
Fosphenytoin DMOX3LB Major Accelerated clearance of Tacrolimus due to the transporter induction by Fosphenytoin. Epilepsy/seizure [8A61-8A6Z] [26]
Phenobarbital DMXZOCG Major Increased metabolism of Tacrolimus caused by Phenobarbital mediated induction of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [26]
Tazemetostat DMWP1BH Moderate Increased metabolism of Tacrolimus caused by Tazemetostat mediated induction of CYP450 enzyme. Follicular lymphoma [2A80] [21]
Solifenacin DMG592Q Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Solifenacin. Functional bladder disorder [GC50] [24]
Tolterodine DMSHPW8 Moderate Increased plasma concentrations of Tacrolimus and Tolterodine due to competitive inhibition of the same metabolic pathway. Functional bladder disorder [GC50] [22]
Itraconazole DMCR1MV Major Decreased metabolism of Tacrolimus caused by Itraconazole mediated inhibition of CYP450 enzyme. Fungal infection [1F29-1F2F] [32]
Miconazole DMPMYE8 Moderate Decreased metabolism of Tacrolimus caused by Miconazole mediated inhibition of CYP450 enzyme. Fungal infection [1F29-1F2F] [52]
Ketoconazole DMPZI3Q Major Decreased metabolism of Tacrolimus caused by Ketoconazole mediated inhibition of CYP450 enzyme. Fungal infection [1F29-1F2F] [32]
Ripretinib DM958QB Moderate Decreased clearance of Tacrolimus due to the transporter inhibition by Ripretinib. Gastrointestinal stromal tumour [2B5B] [21]
Sunitinib DMCBJSR Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Sunitinib. Gastrointestinal stromal tumour [2B5B] [24]
Sulfinpyrazone DMEV954 Moderate Increased metabolism of Tacrolimus caused by Sulfinpyrazone mediated induction of CYP450 enzyme. Gout [FA25] [21]
Digitoxin DMWVIGP Moderate Increased plasma concentrations of Tacrolimus and Digitoxin due to competitive inhibition of the same metabolic pathway. Heart failure [BD10-BD1Z] [22]
Boceprevir DMBSHMF Major Decreased metabolism of Tacrolimus caused by Boceprevir mediated inhibition of CYP450 enzyme. Hepatitis virus infection [1E50-1E51] [21]
Simeprevir DMLUA9D Moderate Decreased metabolism of Tacrolimus caused by Simeprevir mediated inhibition of CYP450 enzyme. Hepatitis virus infection [1E50-1E51] [21]
Telaprevir DMMRV29 Major Decreased clearance of Tacrolimus due to the transporter inhibition by Telaprevir. Hepatitis virus infection [1E50-1E51] [21]
177Lu-DOTATATE DMT8GVU Major Increased risk of nephrotoxicity by the combination of Tacrolimus and 177Lu-DOTATATE. Hepatitis virus infection [1E50-1E51] [22]
Rifampin DMA8J1G Major Accelerated clearance of Tacrolimus due to the transporter induction by Rifampin. HIV-infected patients with tuberculosis [1B10-1B14] [26]
Rifapentine DMCHV4I Major Increased metabolism of Tacrolimus caused by Rifapentine mediated induction of CYP450 enzyme. HIV-infected patients with tuberculosis [1B10-1B14] [26]
Brentuximab vedotin DMWLC57 Moderate Decreased clearance of Tacrolimus due to the transporter inhibition by Brentuximab vedotin. Hodgkin lymphoma [2B30] [53]
MK-1439 DM215WE Minor Increased metabolism of Tacrolimus caused by MK-1439 mediated induction of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [29]
Fosamprenavir DM4W9B3 Major Decreased metabolism of Tacrolimus caused by Fosamprenavir mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [54]
Fostemsavir DM50ILT Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Fostemsavir. Human immunodeficiency virus disease [1C60-1C62] [55]
Cobicistat DM6L4H2 Major Decreased metabolism of Tacrolimus caused by Cobicistat mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [32]
Tipranavir DM8HJX6 Moderate Accelerated clearance of Tacrolimus due to the transporter induction by Tipranavir. Human immunodeficiency virus disease [1C60-1C62] [56]
Etravirine DMGV8QU Moderate Increased metabolism of Tacrolimus caused by Etravirine mediated induction of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [21]
Rilpivirine DMJ0QOW Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Rilpivirine. Human immunodeficiency virus disease [1C60-1C62] [24]
Darunavir DMN3GCH Major Decreased metabolism of Tacrolimus caused by Darunavir mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [54]
Atazanavir DMSYRBX Major Decreased metabolism of Tacrolimus caused by Atazanavir mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [54]
Teriflunomide DMQ2FKJ Major Additive immunosuppressive effects by the combination of Tacrolimus and Teriflunomide. Hyper-lipoproteinaemia [5C80] [57]
Eprosartan DM07K2I Moderate Increased risk of hyperkalemia by the combination of Tacrolimus and Eprosartan. Hypertension [BA00-BA04] [58]
Aliskiren DM1BV7W Moderate Decreased clearance of Tacrolimus due to the transporter inhibition by Aliskiren. Hypertension [BA00-BA04] [24]
Captopril DM458UM Moderate Increased risk of hyperkalemia by the combination of Tacrolimus and Captopril. Hypertension [BA00-BA04] [58]
TAK-491 DMCF6SX Moderate Increased risk of hyperkalemia by the combination of Tacrolimus and TAK-491. Hypertension [BA00-BA04] [58]
Felodipine DMOSW35 Moderate Increased plasma concentrations of Tacrolimus and Felodipine due to competitive inhibition of the same metabolic pathway. Hypertension [BA00-BA04] [22]
Quinapril DMR8H31 Moderate Decreased absorption of Tacrolimus due to formation of complexes caused by Quinapril. Hypertension [BA00-BA04] [29]
Telmisartan DMS3GX2 Moderate Increased risk of hyperkalemia by the combination of Tacrolimus and Telmisartan. Hypertension [BA00-BA04] [58]
Irbesartan DMTP1DC Moderate Increased risk of hyperkalemia by the combination of Tacrolimus and Irbesartan. Hypertension [BA00-BA04] [58]
Conivaptan DM1V329 Major Decreased metabolism of Tacrolimus caused by Conivaptan mediated inhibition of CYP450 enzyme. Hypo-osmolality/hyponatraemia [5C72] [32]
Givosiran DM5PFIJ Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Givosiran. Inborn porphyrin/heme metabolism error [5C58] [22]
Lesinurad DMUR64T Moderate Increased metabolism of Tacrolimus caused by Lesinurad mediated induction of CYP450 enzyme. Inborn purine/pyrimidine/nucleotide metabolism error [5C55] [59]
Balsalazide DM7I1T9 Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Balsalazide. Indeterminate colitis [DD72] [22]
Meclofenamic acid DM05FXR Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Meclofenamic acid. Inflammatory spondyloarthritis [FA92] [22]
Berotralstat DMWA2DZ Moderate Decreased metabolism of Tacrolimus caused by Berotralstat mediated inhibition of CYP450 enzyme. Innate/adaptive immunodeficiency [4A00] [21]
Amobarbital DM0GQ8N Moderate Increased metabolism of Tacrolimus caused by Amobarbital mediated induction of CYP450 enzyme. Insomnia [7A00-7A0Z] [21]
Triazolam DMETYK5 Moderate Increased plasma concentrations of Tacrolimus and Triazolam due to competitive inhibition of the same metabolic pathway. Insomnia [7A00-7A0Z] [22]
Zaleplon DMGFWSM Moderate Increased plasma concentrations of Tacrolimus and Zaleplon due to competitive inhibition of the same metabolic pathway. Insomnia [7A00-7A0Z] [22]
ITI-007 DMUQ1DO Moderate Increased plasma concentrations of Tacrolimus and ITI-007 due to competitive inhibition of the same metabolic pathway. Insomnia [7A00-7A0Z] [22]
Quazepam DMY4D87 Moderate Increased plasma concentrations of Tacrolimus and Quazepam due to competitive inhibition of the same metabolic pathway. Insomnia [7A00-7A0Z] [22]
Estazolam DMZGXUM Moderate Increased plasma concentrations of Tacrolimus and Estazolam due to competitive inhibition of the same metabolic pathway. Insomnia [7A00-7A0Z] [22]
Polyethylene glycol DM4I1JP Moderate Increased risk of ventricular arrhythmias by the combination of Tacrolimus and Polyethylene glycol. Irritable bowel syndrome [DD91] [29]
Naloxegol DML0B41 Minor Decreased clearance of Tacrolimus due to the transporter inhibition by Naloxegol. Large intestine motility disorder [DB32] [60]
Glycerol phenylbutyrate DMDGRQO Moderate Increased metabolism of Tacrolimus caused by Glycerol phenylbutyrate mediated induction of CYP450 enzyme. Liver disease [DB90-DB9Z] [29]
Denosumab DMNI0KO Moderate Additive immunosuppressive effects by the combination of Tacrolimus and Denosumab. Low bone mass disorder [FB83] [61]
Crizotinib DM4F29C Major Increased risk of prolong QT interval by the combination of Tacrolimus and Crizotinib. Lung cancer [2C25] [62]
Brigatinib DM7W94S Moderate Increased metabolism of Tacrolimus caused by Brigatinib mediated induction of CYP450 enzyme. Lung cancer [2C25] [21]
Ceritinib DMB920Z Major Decreased metabolism of Tacrolimus caused by Ceritinib mediated inhibition of CYP450 enzyme. Lung cancer [2C25] [32]
PF-06463922 DMKM7EW Moderate Increased metabolism of Tacrolimus caused by PF-06463922 mediated induction of CYP450 enzyme. Lung cancer [2C25] [63]
Osimertinib DMRJLAT Moderate Decreased metabolism of Tacrolimus caused by Osimertinib mediated inhibition of CYP450 enzyme. Lung cancer [2C25] [29]
Capmatinib DMYCXKL Moderate Decreased clearance of Tacrolimus due to the transporter inhibition by Capmatinib. Lung cancer [2C25] [64]
Selpercatinib DMZR15V Major Increased risk of prolong QT interval by the combination of Tacrolimus and Selpercatinib. Lung cancer [2C25] [29]
Lumefantrine DM29GAD Major Increased risk of prolong QT interval by the combination of Tacrolimus and Lumefantrine. Malaria [1F40-1F45] [21]
Halofantrine DMOMK1V Major Increased risk of prolong QT interval by the combination of Tacrolimus and Halofantrine. Malaria [1F40-1F45] [65]
Primaquine DMWQ16I Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Primaquine. Malaria [1F40-1F45] [24]
Inotuzumab ozogamicin DMAC130 Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Inotuzumab ozogamicin. Malignant haematopoietic neoplasm [2B33] [29]
Idelalisib DM602WT Major Decreased metabolism of Tacrolimus caused by Idelalisib mediated inhibition of CYP450 enzyme. Mature B-cell leukaemia [2A82] [32]
GDC-0199 DMH0QKA Major Decreased clearance of Tacrolimus due to the transporter inhibition by GDC-0199. Mature B-cell leukaemia [2A82] [21]
Moxetumomab pasudotox DMN63DZ Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Moxetumomab pasudotox. Mature B-cell leukaemia [2A82] [22]
IPI-145 DMWA24P Moderate Decreased metabolism of Tacrolimus caused by IPI-145 mediated inhibition of CYP450 enzyme. Mature B-cell leukaemia [2A82] [21]
Arsenic trioxide DM61TA4 Major Increased risk of ventricular arrhythmias by the combination of Tacrolimus and Arsenic trioxide. Mature B-cell lymphoma [2A85] [66]
Blinatumomab DMGECIJ Moderate Decreased metabolism of Tacrolimus caused by Blinatumomab mediated inhibition of CYP450 enzyme. Mature B-cell lymphoma [2A85] [67]
Ibrutinib DMHZCPO Moderate Decreased clearance of Tacrolimus due to the transporter inhibition by Ibrutinib. Mature B-cell lymphoma [2A85] [29]
Arry-162 DM1P6FR Moderate Decreased clearance of Tacrolimus due to the transporter inhibition by Arry-162. Melanoma [2C30] [21]
Vemurafenib DM62UG5 Major Increased risk of prolong QT interval by the combination of Tacrolimus and Vemurafenib. Melanoma [2C30] [24]
LGX818 DMNQXV8 Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and LGX818. Melanoma [2C30] [68]
Dabrafenib DMX6OE3 Moderate Increased metabolism of Tacrolimus caused by Dabrafenib mediated induction of CYP450 enzyme. Melanoma [2C30] [21]
Ethinyl estradiol DMODJ40 Moderate Increased plasma concentrations of Tacrolimus and Ethinyl estradiol due to competitive inhibition of the same metabolic pathway. Menopausal disorder [GA30] [22]
Danazol DML8KTN Moderate Decreased metabolism of Tacrolimus caused by Danazol mediated inhibition of CYP450 enzyme. Menstrual cycle bleeding disorder [GA20] [22]
Almogran DM7I64Z Moderate Increased plasma concentrations of Tacrolimus and Almogran due to competitive inhibition of the same metabolic pathway. Migraine [8A80] [22]
Rimegepant DMHOAUG Moderate Decreased clearance of Tacrolimus due to the transporter inhibition by Rimegepant. Migraine [8A80] [69]
Exjade DMHPRWG Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Exjade. Mineral absorption/transport disorder [5C64] [70]
Lanthanum carbonate DMMJQSH Moderate Decreased absorption of Tacrolimus due to formation of complexes caused by Lanthanum carbonate. Mineral absorption/transport disorder [5C64] [24]
Gallium nitrate DMF9O6B Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Gallium nitrate. Mineral excesses [5B91] [22]
Panobinostat DM58WKG Major Increased risk of prolong QT interval by the combination of Tacrolimus and Panobinostat. Multiple myeloma [2A83] [71]
Thalidomide DM70BU5 Moderate Increased risk of ventricular arrhythmias by the combination of Tacrolimus and Thalidomide. Multiple myeloma [2A83] [21]
Tecfidera DM2OVDT Moderate Additive immunosuppressive effects by the combination of Tacrolimus and Tecfidera. Multiple sclerosis [8A40] [72]
Siponimod DM2R86O Major Additive immunosuppressive effects by the combination of Tacrolimus and Siponimod. Multiple sclerosis [8A40] [21]
Fingolimod DM5JVAN Major Additive immunosuppressive effects by the combination of Tacrolimus and Fingolimod. Multiple sclerosis [8A40] [73]
Ocrelizumab DMEZ2KH Moderate Additive immunosuppressive effects by the combination of Tacrolimus and Ocrelizumab. Multiple sclerosis [8A40] [74]
Ozanimod DMT6AM2 Major Additive immunosuppressive effects by the combination of Tacrolimus and Ozanimod. Multiple sclerosis [8A40] [29]
Deflazacort DMV0RNS Moderate Increased plasma concentrations of Tacrolimus and Deflazacort due to competitive inhibition of the same metabolic pathway. Muscular dystrophy [8C70] [22]
Romidepsin DMT5GNL Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Romidepsin. Mycosis fungoides [2B01] [24]
Fedratinib DM4ZBK6 Moderate Decreased metabolism of Tacrolimus caused by Fedratinib mediated inhibition of CYP450 enzyme. Myeloproliferative neoplasm [2A20] [21]
Nilotinib DM7HXWT Major Increased risk of prolong QT interval by the combination of Tacrolimus and Nilotinib. Myeloproliferative neoplasm [2A20] [24]
Dasatinib DMJV2EK Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Dasatinib. Myeloproliferative neoplasm [2A20] [75]
Omacetaxine mepesuccinate DMPU2WX Moderate Additive immunosuppressive effects by the combination of Tacrolimus and Omacetaxine mepesuccinate. Myeloproliferative neoplasm [2A20] [76]
Busulfan DMXYJ9C Moderate Increased plasma concentrations of Tacrolimus and Busulfan due to competitive inhibition of the same metabolic pathway. Myeloproliferative neoplasm [2A20] [22]
Promethazine DM6I5GR Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Promethazine. Nausea/vomiting [MD90] [24]
Netupitant DMEKAYI Moderate Decreased metabolism of Tacrolimus caused by Netupitant mediated inhibition of CYP450 enzyme. Nausea/vomiting [MD90] [21]
Metoclopramide DMFA5MY Moderate Altered absorption of Tacrolimus due to GI dynamics variation caused by Metoclopramide. Nausea/vomiting [MD90] [77]
Granisetron DMIUW25 Moderate Increased plasma concentrations of Tacrolimus and Granisetron due to competitive inhibition of the same metabolic pathway. Nausea/vomiting [MD90] [22]
Ondansetron DMOTQ1I Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Ondansetron. Nausea/vomiting [MD90] [24]
Entrectinib DMMPTLH Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Entrectinib. Non-small cell lung cancer [2C25] [21]
Sibutramine DMFJTDI Moderate Increased plasma concentrations of Tacrolimus and Sibutramine due to competitive inhibition of the same metabolic pathway. Obesity [5B80-5B81] [22]
Benzphetamine DMIJATC Moderate Increased plasma concentrations of Tacrolimus and Benzphetamine due to competitive inhibition of the same metabolic pathway. Obesity [5B80-5B81] [22]
Levomethadyl Acetate DM06HG5 Major Increased risk of prolong QT interval by the combination of Tacrolimus and Levomethadyl Acetate. Opioid use disorder [6C43] [29]
Lofexidine DM1WXA6 Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Lofexidine. Opioid use disorder [6C43] [24]
S-297995 DM26IH8 Moderate Decreased clearance of Tacrolimus due to the transporter inhibition by S-297995. Opioid use disorder [6C43] [29]
Rucaparib DM9PVX8 Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Rucaparib. Ovarian cancer [2C73] [24]
Ibuprofen DM8VCBE Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Ibuprofen. Pain [MG30-MG3Z] [22]
Buprenorphine DMPRI8G Moderate Increased plasma concentrations of Tacrolimus and Buprenorphine due to competitive inhibition of the same metabolic pathway. Pain [MG30-MG3Z] [22]
Triclabendazole DMPWGBR Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Triclabendazole. Parasitic worm infestation [1F90] [24]
Pimavanserin DMR7IVC Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Pimavanserin. Parkinsonism [8A00] [78]
Bromocriptine DMVE3TK Moderate Decreased metabolism of Tacrolimus caused by Bromocriptine mediated inhibition of CYP450 enzyme. Parkinsonism [8A00] [21]
Abametapir DM2RX0I Moderate Decreased metabolism of Tacrolimus caused by Abametapir mediated inhibition of CYP450 enzyme. Pediculosis [1G00] [79]
Famotidine DMRL3AB Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Famotidine. Peptic ulcer [DA61] [21]
Macimorelin DMQYJIR Major Increased risk of prolong QT interval by the combination of Tacrolimus and Macimorelin. Pituitary gland disorder [5A60-5A61] [80]
Lefamulin DME6G97 Major Increased risk of prolong QT interval by the combination of Tacrolimus and Lefamulin. Pneumonia [CA40] [81]
Bromfenac DMKB79O Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Bromfenac. Postoperative inflammation [1A00-CA43] [22]
Ergonovine DM0VEC1 Moderate Increased plasma concentrations of Tacrolimus and Ergonovine due to competitive inhibition of the same metabolic pathway. Postpartum haemorrhage [JA43] [22]
Lonafarnib DMGM2Z6 Major Decreased metabolism of Tacrolimus caused by Lonafarnib mediated inhibition of CYP450 enzyme. Premature ageing appearance [LD2B] [32]
Ritodrine DM4V6RL Moderate Increased risk of ventricular arrhythmias by the combination of Tacrolimus and Ritodrine. Preterm labour/delivery [JB00] [34]
Degarelix DM3O8QY Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Degarelix. Prostate cancer [2C82] [29]
ABIRATERONE DM8V75C Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and ABIRATERONE. Prostate cancer [2C82] [29]
Enzalutamide DMGL19D Major Increased metabolism of Tacrolimus caused by Enzalutamide mediated induction of CYP450 enzyme. Prostate cancer [2C82] [26]
Relugolix DMK7IWL Major Decreased clearance of Tacrolimus due to the transporter inhibition by Relugolix. Prostate cancer [2C82] [82]
Bicalutamide DMZMSPF Moderate Decreased metabolism of Tacrolimus caused by Bicalutamide mediated inhibition of CYP450 enzyme. Prostate cancer [2C82] [21]
Silodosin DMJSBT6 Moderate Decreased clearance of Tacrolimus due to the transporter inhibition by Silodosin. Prostate hyperplasia [GA90] [83]
Dutasteride DMQ4TJK Moderate Increased plasma concentrations of Tacrolimus and Dutasteride due to competitive inhibition of the same metabolic pathway. Prostate hyperplasia [GA90] [22]
Finasteride DMWV3TZ Moderate Increased plasma concentrations of Tacrolimus and Finasteride due to competitive inhibition of the same metabolic pathway. Prostate hyperplasia [GA90] [22]
Ustekinumab DMHTYK3 Moderate Additive myelosuppressive effects by the combination of Tacrolimus and Ustekinumab. Psoriasis [EA90] [29]
Tildrakizumab DMLW9HG Moderate Additive myelosuppressive effects by the combination of Tacrolimus and Tildrakizumab. Psoriasis [EA90] [29]
Risankizumab DMM32GT Moderate Additive immunosuppressive effects by the combination of Tacrolimus and Risankizumab. Psoriasis [EA90] [29]
Ixekizumab DMXW92T Moderate Additive myelosuppressive effects by the combination of Tacrolimus and Ixekizumab. Psoriasis [EA90] [29]
Levomepromazine DMIKFEL Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Levomepromazine. Psychotic disorder [6A20-6A25] [24]
Riociguat DMXBLMP Moderate Decreased clearance of Tacrolimus due to the transporter inhibition by Riociguat. Pulmonary hypertension [BB01] [21]
Gatifloxacin DMSL679 Major Increased risk of prolong QT interval by the combination of Tacrolimus and Gatifloxacin. Respiratory infection [CA07-CA4Z] [84]
Colistimethate DMZ9BMU Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Colistimethate. Respiratory infection [CA07-CA4Z] [22]
Salsalate DM13P4C Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Salsalate. Rheumatoid arthritis [FA20] [22]
Tocilizumab DM7J6OR Moderate Additive immunosuppressive effects by the combination of Tacrolimus and Tocilizumab. Rheumatoid arthritis [FA20] [29]
Canakinumab DM8HLO5 Moderate Additive immunosuppressive effects by the combination of Tacrolimus and Canakinumab. Rheumatoid arthritis [FA20] [29]
Rilonacept DMGLUQS Moderate Additive myelosuppressive effects by the combination of Tacrolimus and Rilonacept. Rheumatoid arthritis [FA20] [29]
Golimumab DMHZV7X Major Additive immunosuppressive effects by the combination of Tacrolimus and Golimumab. Rheumatoid arthritis [FA20] [85]
Dexamethasone DMMWZET Moderate Increased metabolism of Tacrolimus caused by Dexamethasone mediated induction of CYP450 enzyme. Rheumatoid arthritis [FA20] [21]
Sarilumab DMOGNXY Moderate Additive myelosuppressive effects by the combination of Tacrolimus and Sarilumab. Rheumatoid arthritis [FA20] [29]
Leflunomide DMR8ONJ Major Additive immunosuppressive effects by the combination of Tacrolimus and Leflunomide. Rheumatoid arthritis [FA20] [57]
Quetiapine DM1N62C Moderate Increased plasma concentrations of Tacrolimus and Quetiapine due to competitive inhibition of the same metabolic pathway. Schizophrenia [6A20] [22]
Aripiprazole DM3NUMH Moderate Increased plasma concentrations of Tacrolimus and Aripiprazole due to competitive inhibition of the same metabolic pathway. Schizophrenia [6A20] [22]
Iloperidone DM6AUFY Major Increased risk of prolong QT interval by the combination of Tacrolimus and Iloperidone. Schizophrenia [6A20] [24]
Paliperidone DM7NPJS Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Paliperidone. Schizophrenia [6A20] [24]
Amisulpride DMSJVAM Major Increased risk of prolong QT interval by the combination of Tacrolimus and Amisulpride. Schizophrenia [6A20] [86]
Asenapine DMSQZE2 Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Asenapine. Schizophrenia [6A20] [24]
Pimozide DMW83TP Major Increased risk of prolong QT interval by the combination of Tacrolimus and Pimozide. Schizophrenia [6A20] [29]
Anthrax vaccine DM9GSWY Moderate Antagonize the effect of Tacrolimus when combined with Anthrax vaccine. Sepsis [1G40-1G41] [87]
Voxelotor DMCS6M5 Moderate Decreased metabolism of Tacrolimus caused by Voxelotor mediated inhibition of CYP450 enzyme. Sickle-cell disorder [3A51] [21]
Telotristat ethyl DMDIYFZ Moderate Increased metabolism of Tacrolimus caused by Telotristat ethyl mediated induction of CYP450 enzyme. Small intestine developmental anomaly [DA90] [29]
Larotrectinib DM26CQR Moderate Decreased metabolism of Tacrolimus caused by Larotrectinib mediated inhibition of CYP450 enzyme. Solid tumour/cancer [2A00-2F9Z] [21]
Methylprednisolone DM4BDON Moderate Increased plasma concentrations of Tacrolimus and Methylprednisolone due to competitive inhibition of the same metabolic pathway. Solid tumour/cancer [2A00-2F9Z] [22]
Ifosfamide DMCT3I8 Moderate Increased plasma concentrations of Tacrolimus and Ifosfamide due to competitive inhibition of the same metabolic pathway. Solid tumour/cancer [2A00-2F9Z] [22]
Docetaxel DMDI269 Moderate Increased plasma concentrations of Tacrolimus and Docetaxel due to competitive inhibition of the same metabolic pathway. Solid tumour/cancer [2A00-2F9Z] [22]
Armodafinil DMGB035 Moderate Increased metabolism of Tacrolimus caused by Armodafinil mediated induction of CYP450 enzyme. Solid tumour/cancer [2A00-2F9Z] [21]
LEE011 DMMX75K Major Increased risk of prolong QT interval by the combination of Tacrolimus and LEE011. Solid tumour/cancer [2A00-2F9Z] [24]
Vandetanib DMRICNP Major Increased risk of prolong QT interval by the combination of Tacrolimus and Vandetanib. Solid tumour/cancer [2A00-2F9Z] [24]
Triptorelin DMTK4LS Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Triptorelin. Solid tumour/cancer [2A00-2F9Z] [29]
Taxol DMUOT9V Moderate Increased plasma concentrations of Tacrolimus and Taxol due to competitive inhibition of the same metabolic pathway. Solid tumour/cancer [2A00-2F9Z] [22]
Doxorubicin DMVP5YE Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Doxorubicin. Solid tumour/cancer [2A00-2F9Z] [24]
Telavancin DM58VQX Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Telavancin. Staphylococcal/streptococcal disease [1B5Y] [22]
Pomalidomide DMTGBAX Moderate Decreased metabolism of Tacrolimus caused by Pomalidomide mediated inhibition of CYP450 enzyme. Systemic sclerosis [4A42] [21]
Fostamatinib DM6AUHV Moderate Decreased clearance of Tacrolimus due to the transporter inhibition by Fostamatinib. Thrombocytopenia [3B64] [88]
Lusutrombopag DMH6IKO Moderate Decreased clearance of Tacrolimus due to the transporter inhibition by Lusutrombopag. Thrombocytopenia [3B64] [89]
Apixaban DM89JLN Moderate Decreased clearance of Tacrolimus due to the transporter inhibition by Apixaban. Thrombosis [DB61-GB90] [29]
Brilinta DMBR01X Moderate Decreased metabolism of Tacrolimus caused by Brilinta mediated inhibition of CYP450 enzyme. Thrombosis [DB61-GB90] [29]
Lenvatinib DMB1IU4 Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Lenvatinib. Thyroid cancer [2D10] [24]
Cabozantinib DMIYDT4 Major Increased risk of prolong QT interval by the combination of Tacrolimus and Cabozantinib. Thyroid cancer [2D10] [29]
Papaverine DMCA9QP Major Increased risk of prolong QT interval by the combination of Tacrolimus and Papaverine. Tonus and reflex abnormality [MB47] [90]
Olsalazine DMZW9HA Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Olsalazine. Ulcerative colitis [DD71] [22]
Plazomicin DMKMBES Major Increased risk of nephrotoxicity by the combination of Tacrolimus and Plazomicin. Urinary tract infection [GC08] [22]
Elagolix DMB2C0E Moderate Increased metabolism of Tacrolimus caused by Elagolix mediated induction of CYP450 enzyme. Uterine fibroid [2E86] [21]
Trimeprazine DMEMV9D Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Trimeprazine. Vasomotor/allergic rhinitis [CA08] [91]
Procainamide DMNMXR8 Major Increased risk of prolong QT interval by the combination of Tacrolimus and Procainamide. Ventricular tachyarrhythmia [BC71] [24]
Propafenone DMPIBJK Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Propafenone. Ventricular tachyarrhythmia [BC71] [24]
Flecainide DMSQDLE Moderate Increased risk of prolong QT interval by the combination of Tacrolimus and Flecainide. Ventricular tachyarrhythmia [BC71] [24]
Amiodarone DMUTEX3 Major Increased risk of prolong QT interval by the combination of Tacrolimus and Amiodarone. Ventricular tachyarrhythmia [BC71] [24]
Ganciclovir DM1MBYQ Moderate Increased risk of nephrotoxicity by the combination of Tacrolimus and Ganciclovir. Virus infection [1A24-1D9Z] [21]
Valganciclovir DMS2IUH Moderate Increased risk of lowers seizure threshold by the combination of Tacrolimus and Valganciclovir. Virus infection [1A24-1D9Z] [21]
⏷ Show the Full List of 283 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
Butylated hydroxytoluene E00336 31404 Antioxidant
D&C red no. 28 E00491 6097185 Colorant
D&C red no. 33 E00261 19116 Colorant
FD&C blue no. 1 E00263 19700 Colorant
FD&C blue no. 2 E00446 2723854 Colorant
Quinoline yellow WS E00309 24671 Colorant
Sodium lauryl sulfate E00464 3423265 Emulsifying agent; Modified-release agent; Penetration agent; Solubilizing agent; Surfactant; lubricant
Ammonia E00007 222 Alkalizing agent
Beta-D-lactose E00099 6134 Diluent; Dry powder inhaler carrier; Lyophilization aid
Butyl alcohol E00011 263 Flavoring agent; Solvent
Carmellose sodium E00625 Not Available Disintegrant
Eisenoxyd E00585 56841934 Colorant
FD&C red no. 3 E00629 Not Available Colorant
Ferric hydroxide oxide yellow E00539 23320441 Colorant
Ferrosoferric oxide E00231 14789 Colorant
Lactose monohydrate E00393 104938 Binding agent; Diluent; Dry powder inhaler carrier; Lyophilization aid
Magnesium stearate E00208 11177 lubricant
Poloxamer 188 E00645 Not Available Emulsifying agent; Solubilizing agent; Surfactant
Polyethylene glycol 6000 E00655 Not Available Coating agent; Diluent; Ointment base; Plasticizing agent; Solvent; Suppository base; lubricant
Potassium hydroxide E00233 14797 Alkalizing agent
Propylene glycol E00040 1030 Antimicrobial preservative; Humectant; Plasticizing agent; Solvent
Silicon dioxide E00670 Not Available Anticaking agent; Opacifying agent; Viscosity-controlling agent
Tartaric acid E00029 875 Acidulant; Complexing agent; Flavoring agent
Titanium dioxide E00322 26042 Coating agent; Colorant; Opacifying agent
⏷ Show the Full List of 25 Pharmaceutical Excipients of This Drug
Pharmaceutical Formulation
Formulation Name Drug Dosage Dosage Form Route
Tacrolimus 0.75 mg tablet 0.75 mg 24 HR Extended Release Oral Tablet Oral
Tacrolimus 1 mg tablet 1 mg 24 HR Extended Release Oral Tablet Oral
Tacrolimus 4 mg tablet 4 mg 24 HR Extended Release Oral Tablet Oral
Tacrolimus 1 mg capsule 1 mg Oral Capsule Oral
Tacrolimus 0.5 mg capsule 0.5 mg Oral Capsule Oral
Tacrolimus 5 mg capsule 5 mg Oral Capsule Oral
Jump to Detail Pharmaceutical Formulation Page of This Drug

References

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