General Information of Drug (ID: DM58WKG)

Drug Name
Panobinostat
Synonyms
Faridak; LBH 589; LBH589; LBH-589; LBH-589B; NVP-LBH589; NVP-LBH-589; Panobinostat, NVP-LBH589, LBH589; (E)-N-HYDROXY-3-(4-{[2-(2-METHYL-1H-INDOL-3-YL)-ETHYLAMINO]-METHYL}-PHENYL)-ACRYLAMIDE; (E)-N-hydroxy-3-[4-[[2-(2-methyl-1H-indol-3-yl)ethylamino]methyl]phenyl]prop-2-enamide
Indication
Disease Entry ICD 11 Status REF
Chronic graft versus host disease N.A. Approved [1]
Lung cancer 2C25.0 Approved [1]
Multiple myeloma 2A83 Approved [2]
Non-small-cell lung cancer 2C25.Y Approved [1]
Plasma cell myeloma 2A83.1 Approved [1]
Primary cutaneous T-cell lymphoma N.A. Approved [1]
Type-2 diabetes 5A11 Phase 3 [3]
Primary myelofibrosis 2A20.2 Phase 2 [3]
⏷ Show the Full List of Indication(s)
Drug Type
Small molecular drug
Structure
3D MOL 2D MOL
#Ro5 Violations (Lipinski): 0 Molecular Weight (mw) 349.4
Logarithm of the Partition Coefficient (xlogp) 3
Rotatable Bond Count (rotbonds) 7
Hydrogen Bond Donor Count (hbonddonor) 4
Hydrogen Bond Acceptor Count (hbondacc) 3
ADMET Property
Absorption Tmax
The time to maximum plasma concentration (Tmax) is 2 h []
Clearance
The drug present in the plasma can be removed from the body at the rate of 10.2 mL/min/kg [4]
Half-life
The concentration or amount of drug in body reduced by one-half in 30 hours [4]
Unbound Fraction
The unbound fraction of drug in plasma is 0.1% [4]
Adverse Drug Reaction (ADR)
ADR Term Variation Related DOT DOT ID REF
Cerebrovascular disorder Not Available NAA15 OT53SIZG [5]
Platelet aggregation Not Available CBS OT46FSKD [5]
Platelet aggregation Not Available MTHFR OTUBJSR7 [5]
Chemical Identifiers
Formula
C21H23N3O2
IUPAC Name
(E)-N-hydroxy-3-[4-[[2-(2-methyl-1H-indol-3-yl)ethylamino]methyl]phenyl]prop-2-enamide
Canonical SMILES
CC1=C(C2=CC=CC=C2N1)CCNCC3=CC=C(C=C3)/C=C/C(=O)NO
InChI
InChI=1S/C21H23N3O2/c1-15-18(19-4-2-3-5-20(19)23-15)12-13-22-14-17-8-6-16(7-9-17)10-11-21(25)24-26/h2-11,22-23,26H,12-14H2,1H3,(H,24,25)/b11-10+
InChIKey
FPOHNWQLNRZRFC-ZHACJKMWSA-N
Cross-matching ID
PubChem CID
6918837
ChEBI ID
CHEBI:85990
CAS Number
404950-80-7
DrugBank ID
DB06603
TTD ID
D0E3SH
VARIDT ID
DR00181
INTEDE ID
DR1234
ACDINA ID
D00507
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
Histone deacetylase 1 (HDAC1) TT6R7JZ HDAC1_HUMAN Inhibitor [6]

Drug Transporter (DTP)
DTP Name DTP ID UniProt ID MOA REF
P-glycoprotein 1 (ABCB1) DTUGYRD MDR1_HUMAN Substrate [7]

Drug-Metabolizing Enzyme (DME)
DME Name DME ID UniProt ID MOA REF
Cytochrome P450 3A4 (CYP3A4) DE4LYSA CP3A4_HUMAN Substrate [8]

Drug Off-Target (DOT)
DOT Name DOT ID UniProt ID Interaction REF
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase epsilon-1 (PLCE1) OTJISZOX PLCE1_HUMAN Gene/Protein Processing [9]
14-3-3 protein sigma (SFN) OTLJCZ1U 1433S_HUMAN Gene/Protein Processing [9]
2-hydroxyacylsphingosine 1-beta-galactosyltransferase OT17ST61 CGT_HUMAN Gene/Protein Processing [9]
3',5'-cyclic-AMP phosphodiesterase 4D (PDE4D) OT1RWFV0 PDE4D_HUMAN Gene/Protein Processing [9]
3-hydroxy-3-methylglutaryl-CoA lyase, cytoplasmic (HMGCLL1) OT9SQ5PU HMGC2_HUMAN Gene/Protein Processing [9]
4-aminobutyrate aminotransferase, mitochondrial (ABAT) OTXAGR7J GABT_HUMAN Gene/Protein Processing [9]
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase 9 (FUT9) OTLIJBQY FUT9_HUMAN Gene/Protein Processing [9]
4-hydroxyphenylpyruvate dioxygenase-like protein (HPDL) OTW7D1SV HPDL_HUMAN Gene/Protein Processing [9]
A disintegrin and metalloproteinase with thrombospondin motifs 15 (ADAMTS15) OTYB6JS3 ATS15_HUMAN Gene/Protein Processing [9]
A disintegrin and metalloproteinase with thrombospondin motifs 19 (ADAMTS19) OTEG5Q2G ATS19_HUMAN Gene/Protein Processing [9]
Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This Drug

Molecular Expression Atlas of This Drug

The Studied Disease Chronic graft versus host disease
ICD Disease Classification
Molecule Name Molecule Type Gene Name p-value Fold-Change Z-score
Histone deacetylase 1 (HDAC1) DTT HDAC1 6.73E-02 0.24 0.59
P-glycoprotein 1 (ABCB1) DTP P-GP 2.55E-01 4.83E-01 5.66E-01
Cytochrome P450 3A4 (CYP3A4) DME CYP3A4 1.10E-01 -1.23E-01 -2.88E-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 Disease Different from Panobinostat (Comorbidity)
DDI Drug Name DDI Drug ID Severity Mechanism Comorbidity REF
Metreleptin DM1NOEK Moderate Increased metabolism of Panobinostat caused by Metreleptin mediated induction of CYP450 enzyme. Acute diabete complication [5A2Y] [10]
Ivosidenib DM8S6T7 Major Increased risk of prolong QT interval by the combination of Panobinostat and Ivosidenib. Acute myeloid leukaemia [2A60] [10]
Arn-509 DMT81LZ Major Increased metabolism of Panobinostat caused by Arn-509 mediated induction of CYP450 enzyme. Acute myeloid leukaemia [2A60] [10]
Gilteritinib DMTI0ZO Major Increased risk of prolong QT interval by the combination of Panobinostat and Gilteritinib. Acute myeloid leukaemia [2A60] [10]
Oliceridine DM6MDCF Major Increased risk of prolong QT interval by the combination of Panobinostat and Oliceridine. Acute pain [MG31] [10]
Ivabradine DM0L594 Major Increased risk of ventricular arrhythmias by the combination of Panobinostat and Ivabradine. Angina pectoris [BA40] [11]
Bedaquiline DM3906J Major Increased risk of prolong QT interval by the combination of Panobinostat and Bedaquiline. Antimicrobial drug resistance [MG50-MG52] [10]
Levalbuterol DM5YBO1 Moderate Increased risk of ventricular arrhythmias by the combination of Panobinostat and Levalbuterol. Asthma [CA23] [12]
Pexidartinib DMS2J0Z Major Increased risk of hepatotoxicity by the combination of Panobinostat and Pexidartinib. Bone/articular cartilage neoplasm [2F7B] [13]
Eribulin DM1DX4Q Major Increased risk of prolong QT interval by the combination of Panobinostat and Eribulin. Breast cancer [2C60-2C6Y] [10]
Tucatinib DMBESUA Major Decreased metabolism of Panobinostat caused by Tucatinib mediated inhibition of CYP450 enzyme. Breast cancer [2C60-2C6Y] [14]
Palbociclib DMD7L94 Moderate Decreased metabolism of Panobinostat caused by Palbociclib mediated inhibition of CYP450 enzyme. Breast cancer [2C60-2C6Y] [14]
Bosutinib DMTI8YE Major Increased risk of prolong QT interval by the combination of Panobinostat and Bosutinib. Breast cancer [2C60-2C6Y] [10]
PF-04449913 DMSB068 Major Increased risk of prolong QT interval by the combination of Panobinostat and PF-04449913. Chronic myelomonocytic leukaemia [2A40] [10]
Olodaterol DM62B78 Moderate Increased risk of prolong QT interval by the combination of Panobinostat and Olodaterol. Chronic obstructive pulmonary disease [CA22] [15]
Vilanterol DMF5EK1 Moderate Increased risk of ventricular arrhythmias by the combination of Panobinostat and Vilanterol. Chronic obstructive pulmonary disease [CA22] [12]
Regorafenib DMHSY1I Major Increased risk of bleeding by the combination of Panobinostat and Regorafenib. Colorectal cancer [2B91] [16]
Ardeparin DMYRX8B Major Increased risk of bleeding by the combination of Panobinostat and Ardeparin. Coronary thrombosis [BA43] [16]
Pasireotide DMHM7JS Major Increased risk of prolong QT interval by the combination of Panobinostat and Pasireotide. Cushing syndrome [5A70] [10]
Osilodrostat DMIJC9X Major Increased risk of prolong QT interval by the combination of Panobinostat and Osilodrostat. Cushing syndrome [5A70] [10]
Ivacaftor DMZC1HS Moderate Decreased metabolism of Panobinostat caused by Ivacaftor mediated inhibition of CYP450 enzyme. Cystic fibrosis [CA25] [14]
MK-8228 DMOB58Q Moderate Decreased metabolism of Panobinostat caused by MK-8228 mediated inhibition of CYP450 enzyme. Cytomegaloviral disease [1D82] [14]
Danaparoid DM6CLBN Major Increased risk of bleeding by the combination of Panobinostat and Danaparoid. Deep vein thrombosis [BD71] [16]
Vortioxetine DM6F1PU Major Increased risk of bleeding by the combination of Panobinostat and Vortioxetine. Depression [6A70-6A7Z] [17]
OPC-34712 DMHG57U Major Decreased metabolism of Panobinostat caused by OPC-34712 mediated inhibition of CYP450 enzyme. Depression [6A70-6A7Z] [18]
Deutetrabenazine DMUPFLI Major Increased risk of prolong QT interval by the combination of Panobinostat and Deutetrabenazine. Dystonic disorder [8A02] [10]
Ingrezza DMVPLNC Major Increased risk of prolong QT interval by the combination of Panobinostat and Ingrezza. Dystonic disorder [8A02] [10]
Stiripentol DMMSDOY Moderate Decreased metabolism of Panobinostat caused by Stiripentol mediated inhibition of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [14]
Eslicarbazepine DMZREFQ Moderate Increased metabolism of Panobinostat caused by Eslicarbazepine mediated induction of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [10]
Cannabidiol DM0659E Moderate Increased risk of hepatotoxicity by the combination of Panobinostat and Cannabidiol. Epileptic encephalopathy [8A62] [11]
Tazemetostat DMWP1BH Moderate Increased metabolism of Panobinostat caused by Tazemetostat mediated induction of CYP450 enzyme. Follicular lymphoma [2A80] [10]
Avapritinib DMK2GZX Major Increased risk of bleeding by the combination of Panobinostat and Avapritinib. Gastrointestinal stromal tumour [2B5B] [16]
Boceprevir DMBSHMF Major Decreased metabolism of Panobinostat caused by Boceprevir mediated inhibition of CYP450 enzyme. Hepatitis virus infection [1E50-1E51] [14]
Fostemsavir DM50ILT Major Increased risk of prolong QT interval by the combination of Panobinostat and Fostemsavir. Human immunodeficiency virus disease [1C60-1C62] [10]
Cobicistat DM6L4H2 Major Decreased metabolism of Panobinostat caused by Cobicistat mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [14]
Rilpivirine DMJ0QOW Major Increased risk of prolong QT interval by the combination of Panobinostat and Rilpivirine. Human immunodeficiency virus disease [1C60-1C62] [10]
Teriflunomide DMQ2FKJ Major Additive myelosuppressive effects by the combination of Panobinostat and Teriflunomide. Hyper-lipoproteinaemia [5C80] [19]
BMS-201038 DMQTAGO Major Increased risk of hepatotoxicity by the combination of Panobinostat and BMS-201038. Hyper-lipoproteinaemia [5C80] [20]
Berotralstat DMWA2DZ Moderate Decreased metabolism of Panobinostat caused by Berotralstat mediated inhibition of CYP450 enzyme. Innate/adaptive immunodeficiency [4A00] [14]
Suvorexant DM0E6S3 Moderate Decreased metabolism of Panobinostat caused by Suvorexant mediated inhibition of CYP450 enzyme. Insomnia [7A00-7A0Z] [14]
Polyethylene glycol DM4I1JP Major Increased risk of ventricular arrhythmias by the combination of Panobinostat and Polyethylene glycol. Irritable bowel syndrome [DD91] [21]
Denosumab DMNI0KO Moderate Additive myelosuppressive effects by the combination of Panobinostat and Denosumab. Low bone mass disorder [FB83] [22]
Crizotinib DM4F29C Major Increased risk of prolong QT interval by the combination of Panobinostat and Crizotinib. Lung cancer [2C25] [10]
Ceritinib DMB920Z Major Decreased metabolism of Panobinostat caused by Ceritinib mediated inhibition of CYP450 enzyme. Lung cancer [2C25] [14]
PF-06463922 DMKM7EW Moderate Increased metabolism of Panobinostat caused by PF-06463922 mediated induction of CYP450 enzyme. Lung cancer [2C25] [10]
Osimertinib DMRJLAT Major Increased risk of prolong QT interval by the combination of Panobinostat and Osimertinib. Lung cancer [2C25] [10]
Lumefantrine DM29GAD Major Increased risk of prolong QT interval by the combination of Panobinostat and Lumefantrine. Malaria [1F40-1F45] [16]
Calaspargase pegol DMQZBXI Moderate Increased risk of hepatotoxicity by the combination of Panobinostat and Calaspargase pegol. Malignant haematopoietic neoplasm [2B33] [23]
Idelalisib DM602WT Moderate Increased risk of hepatotoxicity by the combination of Panobinostat and Idelalisib. Mature B-cell leukaemia [2A82] [24]
IPI-145 DMWA24P Moderate Decreased metabolism of Panobinostat caused by IPI-145 mediated inhibition of CYP450 enzyme. Mature B-cell leukaemia [2A82] [14]
Acalabrutinib DM7GCVW Major Increased risk of bleeding by the combination of Panobinostat and Acalabrutinib. Mature B-cell lymphoma [2A85] [16]
Ibrutinib DMHZCPO Major Increased risk of bleeding by the combination of Panobinostat and Ibrutinib. Mature B-cell lymphoma [2A85] [16]
Arry-162 DM1P6FR Major Increased risk of bleeding by the combination of Panobinostat and Arry-162. Melanoma [2C30] [16]
Vemurafenib DM62UG5 Major Increased risk of prolong QT interval by the combination of Panobinostat and Vemurafenib. Melanoma [2C30] [25]
LGX818 DMNQXV8 Major Increased risk of prolong QT interval by the combination of Panobinostat and LGX818. Melanoma [2C30] [10]
Dabrafenib DMX6OE3 Moderate Increased metabolism of Panobinostat caused by Dabrafenib mediated induction of CYP450 enzyme. Melanoma [2C30] [10]
Tecfidera DM2OVDT Moderate Additive immunosuppressive effects by the combination of Panobinostat and Tecfidera. Multiple sclerosis [8A40] [26]
Siponimod DM2R86O Major Increased risk of ventricular arrhythmias by the combination of Panobinostat and Siponimod. Multiple sclerosis [8A40] [16]
Fingolimod DM5JVAN Major Additive immunosuppressive effects by the combination of Panobinostat and Fingolimod. Multiple sclerosis [8A40] [27]
Ocrelizumab DMEZ2KH Moderate Additive immunosuppressive effects by the combination of Panobinostat and Ocrelizumab. Multiple sclerosis [8A40] [28]
Ozanimod DMT6AM2 Major Increased risk of prolong QT interval by the combination of Panobinostat and Ozanimod. Multiple sclerosis [8A40] [10]
Fedratinib DM4ZBK6 Major Increased risk of bleeding by the combination of Panobinostat and Fedratinib. Myeloproliferative neoplasm [2A20] [16]
Ruxolitinib DM7Q98D Major Increased risk of bleeding by the combination of Panobinostat and Ruxolitinib. Myeloproliferative neoplasm [2A20] [16]
Entrectinib DMMPTLH Major Increased risk of prolong QT interval by the combination of Panobinostat and Entrectinib. Non-small cell lung cancer [2C25] [10]
Nepafenac DMYK490 Moderate Increased risk of bleeding by the combination of Panobinostat and Nepafenac. Osteoarthritis [FA00-FA05] [29]
Rucaparib DM9PVX8 Major Increased risk of prolong QT interval by the combination of Panobinostat and Rucaparib. Ovarian cancer [2C73] [10]
Triclabendazole DMPWGBR Major Increased risk of prolong QT interval by the combination of Panobinostat and Triclabendazole. Parasitic worm infestation [1F90] [10]
Abametapir DM2RX0I Moderate Decreased metabolism of Panobinostat caused by Abametapir mediated inhibition of CYP450 enzyme. Pediculosis [1G00] [30]
Macimorelin DMQYJIR Major Increased risk of prolong QT interval by the combination of Panobinostat and Macimorelin. Pituitary gland disorder [5A60-5A61] [31]
Lefamulin DME6G97 Major Increased risk of prolong QT interval by the combination of Panobinostat and Lefamulin. Pneumonia [CA40] [10]
Degarelix DM3O8QY Major Increased risk of prolong QT interval by the combination of Panobinostat and Degarelix. Prostate cancer [2C82] [10]
Enzalutamide DMGL19D Major Increased metabolism of Panobinostat caused by Enzalutamide mediated induction of CYP450 enzyme. Prostate cancer [2C82] [10]
Relugolix DMK7IWL Major Increased risk of prolong QT interval by the combination of Panobinostat and Relugolix. Prostate cancer [2C82] [10]
Golimumab DMHZV7X Major Additive immunosuppressive effects by the combination of Panobinostat and Golimumab. Rheumatoid arthritis [FA20] [32]
Anthrax vaccine DM9GSWY Moderate Antagonize the effect of Panobinostat when combined with Anthrax vaccine. Sepsis [1G40-1G41] [33]
Voxelotor DMCS6M5 Moderate Decreased metabolism of Panobinostat caused by Voxelotor mediated inhibition of CYP450 enzyme. Sickle-cell disorder [3A51] [14]
Telotristat ethyl DMDIYFZ Moderate Increased metabolism of Panobinostat caused by Telotristat ethyl mediated induction of CYP450 enzyme. Small intestine developmental anomaly [DA90] [11]
Larotrectinib DM26CQR Moderate Decreased metabolism of Panobinostat caused by Larotrectinib mediated inhibition of CYP450 enzyme. Solid tumour/cancer [2A00-2F9Z] [14]
LEE011 DMMX75K Major Increased risk of prolong QT interval by the combination of Panobinostat and LEE011. Solid tumour/cancer [2A00-2F9Z] [10]
Triptorelin DMTK4LS Major Increased risk of prolong QT interval by the combination of Panobinostat and Triptorelin. Solid tumour/cancer [2A00-2F9Z] [10]
Pitolisant DM8RFNJ Major Increased risk of prolong QT interval by the combination of Panobinostat and Pitolisant. Somnolence [MG42] [10]
Plicamycin DM7C8YV Major Increased risk of bleeding by the combination of Panobinostat and Plicamycin. Testicular cancer [2C80] [16]
Fostamatinib DM6AUHV Moderate Decreased metabolism of Panobinostat caused by Fostamatinib mediated inhibition of CYP450 enzyme. Thrombocytopenia [3B64] [34]
Apixaban DM89JLN Major Increased risk of bleeding by the combination of Panobinostat and Apixaban. Thrombosis [DB61-GB90] [16]
Brilinta DMBR01X Moderate Decreased metabolism of Panobinostat caused by Brilinta mediated inhibition of CYP450 enzyme. Thrombosis [DB61-GB90] [14]
Lenvatinib DMB1IU4 Major Increased risk of prolong QT interval by the combination of Panobinostat and Lenvatinib. Thyroid cancer [2D10] [10]
Cabozantinib DMIYDT4 Major Increased risk of prolong QT interval by the combination of Panobinostat and Cabozantinib. Thyroid cancer [2D10] [10]
Elagolix DMB2C0E Moderate Increased metabolism of Panobinostat caused by Elagolix mediated induction of CYP450 enzyme. Uterine fibroid [2E86] [10]
Betrixaban DM2C4RF Major Increased risk of bleeding by the combination of Panobinostat and Betrixaban. Venous thromboembolism [BD72] [16]
⏷ Show the Full List of 89 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
FD&C blue no. 1 E00263 19700 Colorant
Mannitol E00103 6251 Diluent; Flavoring agent; Lyophilization aid; Plasticizing agent; Tonicity agent
Gelatin E00630 Not Available Other agent
Magnesium stearate E00208 11177 lubricant
Titanium dioxide E00322 26042 Coating agent; Colorant; Opacifying agent
Colcothar yellow E00436 518696 Colorant
Haematite red E00236 14833 Colorant
Cellulose microcrystalline E00698 Not Available Adsorbent; Suspending agent; Diluent
Pregelatinized starch E00674 Not Available Binding agent; Diluent; Disintegrant
⏷ Show the Full List of 9 Pharmaceutical Excipients of This Drug
Pharmaceutical Formulation
Formulation Name Drug Dosage Dosage Form Route
Panobinostat 10 mg capsule 10 mg Oral Capsule Oral
Panobinostat 15 mg capsule 15 mg Oral Capsule Oral
Panobinostat 20 mg capsule 20 mg Oral Capsule Oral
Panobinostat Lactate eq 10mg base capsule eq 10mg base Capsule Oral
Panobinostat Lactate eq 15mg base capsule eq 15mg base Capsule Oral
Panobinostat Lactate eq 20mg base capsule eq 20mg base Capsule Oral
Jump to Detail Pharmaceutical Formulation Page of This Drug

References

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2 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services.
3 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: 7489).
4 Trend Analysis of a Database of Intravenous Pharmacokinetic Parameters in Humans for 1352 Drug Compounds
5 ADReCS-Target: target profiles for aiding drug safety research and application. Nucleic Acids Res. 2018 Jan 4;46(D1):D911-D917. doi: 10.1093/nar/gkx899.
6 Protein methyltransferases as a target class for drug discovery. Nat Rev Drug Discov. 2009 Sep;8(9):724-32.
7 Panobinostat for the treatment of multiple myeloma: the evidence to date. J Blood Med. 2015 Oct 8;6:269-76.
8 Panobinostat for the treatment of relapsed or relapsed/refractory multiple myeloma: pharmacology and clinical outcomes. Expert Rev Clin Pharmacol. 2016;9(1):35-48.
9 A transcriptome-based classifier to identify developmental toxicants by stem cell testing: design, validation and optimization for histone deacetylase inhibitors. Arch Toxicol. 2015 Sep;89(9):1599-618.
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26 Product Information. Vumerity (diroximel fumarate). Alkermes, Inc, Cambridge, MA.
27 Product Information. Gilenya (fingolimod). Novartis Pharmaceuticals, East Hanover, NJ.
28 Product Information. Ocrevus (ocrelizumab). Genentech, South San Francisco, CA.
29 Product Information. Acular (ketorolac). Allergan Inc, Irvine, CA.
30 Product Information. Xeglyze (abametapir topical). Dr. Reddy's Laboratories Inc, Upper Saddle River, NJ.
31 Product Information. Macrilen (macimorelin). Aeterna Zentaris, Charleston, SC.
32 Product Information. Cimzia (certolizumab). UCB Pharma Inc, Smyrna, GA.
33 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]
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