4T Basic 2012 PA Criteria Medicare Part Band DPrior Approvals Spanish

MedicarePartBandPartDPriorApprovalsSpanish_old050912 MedicarePartBandPartDPriorApprovalsSpanish_old050912

MedicarePartBandPartDPriorApprovals_Old_04062012 MedicarePartBandPartDPriorApprovals_Old_04062012

User Manual: MedicarePartBandPartDPriorApprovalsSpanish

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP

2012 Prior Authorization Criteria
ACTEMRA .................................................................................................................................................... 20
ACTEMRA® .............................................................................................................................................. 20
ACTIMMUNE ............................................................................................................................................... 21
ACTIMMUNE® ......................................................................................................................................... 21
ADAGEN ...................................................................................................................................................... 22
ADAGEN® ................................................................................................................................................ 22
ADCIRCA ...................................................................................................................................................... 23
ADCIRCA® ................................................................................................................................................ 23
AFINITOR ..................................................................................................................................................... 24
AFINITOR® ............................................................................................................................................... 24
ALDURAZYME .............................................................................................................................................. 25
ALDURAZYME® ........................................................................................................................................ 25
ALPHA1-PROTEINASE INHIBITOR ................................................................................................................ 26
ARALAST NP® .......................................................................................................................................... 26
AMPHETAMINES ......................................................................................................................................... 27
AMPHETAMINE SALT COMBO ................................................................................................................ 27
DEXTROAMPHETAMINE SULFATE ........................................................................................................... 27
AMPYRA ...................................................................................................................................................... 28
AMPYRA® ................................................................................................................................................ 28
ANABOLIC STEROIDS ................................................................................................................................... 29
ANADROL-50® ......................................................................................................................................... 29
OXANDROLONE ....................................................................................................................................... 29
H6864_MMG12_02 File & Use 09212011

GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP
ANAGRELIDE................................................................................................................................................ 30
ANAGRELIDE HCL .................................................................................................................................... 30
ARCALYST .................................................................................................................................................... 31
ARCALYST® .............................................................................................................................................. 31
ATYPICAL ODT ............................................................................................................................................. 32
FAZACLO®................................................................................................................................................ 32
AVONEX....................................................................................................................................................... 33
AVONEX ADMINISTRATION PACK® ......................................................................................................... 33
AVONEX®................................................................................................................................................. 33
B vs D - Part B versus Part D Coverage PA .................................................................................................. 34
ACETYLCYSTEINE ..................................................................................................................................... 34
ADRIAMYCIN ........................................................................................................................................... 34
ALBUTEROL SULFATE .............................................................................................................................. 34
ALIMTA® .................................................................................................................................................. 34
AMIFOSTINE ............................................................................................................................................ 34
AMINOSYN II 3.5% M-DEXTROSE 5%® .................................................................................................... 34
AMINOSYN II 3.5%-DEXTROSE 25%® ...................................................................................................... 34
AMINOSYN II 3.5%-DEXTROSE 5%® ........................................................................................................ 34
AMINOSYN II 4.25%-DEXTROSE 25%® .................................................................................................... 34
AMINOSYN II 5% IN 25% DEXTROSE® ..................................................................................................... 34
AMINOSYN II IN DEXTROSE® ................................................................................................................... 34
AMINOSYN II WITH LYTES-CA-DW® ........................................................................................................ 34

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP
AMINOSYN II® ......................................................................................................................................... 34
AMINOSYN M® ........................................................................................................................................ 34
AMINOSYN® ............................................................................................................................................ 34
AMINOSYN-HBC® .................................................................................................................................... 34
AMINOSYN-HF®....................................................................................................................................... 34
AMINOSYN-PF® ....................................................................................................................................... 34
AMIODARONE HCL .................................................................................................................................. 34
AMPHOTERICIN B .................................................................................................................................... 34
ASTRAMORPH-PF® .................................................................................................................................. 34
AVASTIN® ................................................................................................................................................ 34
AZASAN® ................................................................................................................................................. 34
AZATHIOPRINE ........................................................................................................................................ 34
AZATHIOPRINE SODIUM ......................................................................................................................... 34
BICNU® .................................................................................................................................................... 34
BLEOMYCIN SULFATE .............................................................................................................................. 34
BUDESONIDE ........................................................................................................................................... 34
BUSULFEX® .............................................................................................................................................. 34
CALCITRIOL .............................................................................................................................................. 34
CAMPATH® .............................................................................................................................................. 34
CARBOPLATIN ......................................................................................................................................... 34
CELLCEPT® ............................................................................................................................................... 35
CISPLATIN ................................................................................................................................................ 35

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP
CLADRIBINE ............................................................................................................................................. 35
CLINIMIX E® ............................................................................................................................................. 35
CLINIMIX®................................................................................................................................................ 35
CLINISOL® ................................................................................................................................................ 35
COLISTIMETHATE SODIUM ..................................................................................................................... 35
COSMEGEN® ........................................................................................................................................... 35
CROMOLYN SODIUM .............................................................................................................................. 35
CUBICIN® ................................................................................................................................................. 35
CYCLOPHOSPHAMIDE ............................................................................................................................. 35
CYCLOSPORINE ........................................................................................................................................ 35
CYCLOSPORINE MODIFIED ...................................................................................................................... 35
CYTARABINE ............................................................................................................................................ 35
DACARBAZINE ......................................................................................................................................... 35
DAUNORUBICIN HCL ............................................................................................................................... 35
DEPO-PROVERA®..................................................................................................................................... 35
DEXRAZOXANE ........................................................................................................................................ 35
DIPHTHERIA-TETANUS TOXOID®............................................................................................................. 35
DOXIL®..................................................................................................................................................... 35
DOXORUBICIN HCL .................................................................................................................................. 35
DURAMORPH® ........................................................................................................................................ 35
ELITEK® .................................................................................................................................................... 35
ELSPAR® .................................................................................................................................................. 35

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP
EMEND® .................................................................................................................................................. 35
ENGERIX-B® ............................................................................................................................................. 35
EPIRUBICIN HCL....................................................................................................................................... 35
ETOPOSIDE .............................................................................................................................................. 35
FASLODEX®.............................................................................................................................................. 35
FENTANYL CITRATE ................................................................................................................................. 35
FLUDARABINE PHOSPHATE® ................................................................................................................... 35
FLUOROURACIL ....................................................................................................................................... 35
FREAMINE III WITH ELECTROLYTES® ....................................................................................................... 35
FREAMINE III® ......................................................................................................................................... 35
GAMASTAN S-D® ..................................................................................................................................... 36
GANCICLOVIR SODIUM ........................................................................................................................... 36
GEMZAR® ................................................................................................................................................ 36
GENGRAF................................................................................................................................................. 36
GRANISETRON HCL.................................................................................................................................. 36
HEPARIN SODIUM ................................................................................................................................... 36
HEPARIN SODIUM IN 0.45% NACL .......................................................................................................... 36
HEPARIN SODIUM IN 0.9% NACL ............................................................................................................ 36
HEPARIN SODIUM IN 5% DEXTROSE ....................................................................................................... 36
HEPATAMINE® ........................................................................................................................................ 36
HEPATASOL® ........................................................................................................................................... 36
HERCEPTIN® ............................................................................................................................................ 36

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP
HYDROMORPHONE HCL.......................................................................................................................... 36
IDARUBICIN HCL ...................................................................................................................................... 36
IFEX®........................................................................................................................................................ 36
IFOSFAMIDE ............................................................................................................................................ 36
IFOSFAMIDE-MESNA ............................................................................................................................... 36
INTRALIPID® ............................................................................................................................................ 36
INTRON A® .............................................................................................................................................. 36
IPRATROPIUM BROMIDE ........................................................................................................................ 36
IPRATROPIUM-ALBUTEROL ..................................................................................................................... 36
IRINOTECAN HCL ..................................................................................................................................... 36
ISTODAX® ................................................................................................................................................ 36
LEUCOVORIN CALCIUM ........................................................................................................................... 36
LEVALBUTEROL CONCENTRATE .............................................................................................................. 36
LEVOCARNITINE ...................................................................................................................................... 36
LIPOSYN II® .............................................................................................................................................. 36
LIPOSYN III ............................................................................................................................................... 36
MELPHALAN HCL ..................................................................................................................................... 36
MESNA .................................................................................................................................................... 36
METHOTREXATE ...................................................................................................................................... 36
MIACALCIN® ............................................................................................................................................ 36
MITOMYCIN ............................................................................................................................................ 36
MITOXANTRONE HCL .............................................................................................................................. 36

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP
MORPHINE SULFATE ............................................................................................................................... 37
MUSTARGEN® ......................................................................................................................................... 37
MYCOPHENOLATE MOFETIL ................................................................................................................... 37
MYFORTIC® ............................................................................................................................................. 37
NEORAL® ................................................................................................................................................. 37
NEPHRAMINE® ........................................................................................................................................ 37
NEUMEGA® ............................................................................................................................................. 37
ONDANSETRON HCL................................................................................................................................ 37
ONDANSETRON ODT ............................................................................................................................... 37
ONTAK® ................................................................................................................................................... 37
OXALIPLATIN ........................................................................................................................................... 37
PACLITAXEL ............................................................................................................................................. 37
PENTOSTATIN.......................................................................................................................................... 37
PERFOROMIST® ....................................................................................................................................... 37
PHOTOFRIN® ........................................................................................................................................... 37
PREMASOL® ............................................................................................................................................ 37
PROCALAMINE® ...................................................................................................................................... 37
PROGRAF® ............................................................................................................................................... 37
PROLEUKIN® ............................................................................................................................................ 37
PROSOL® ................................................................................................................................................. 37
PULMOZYME® ......................................................................................................................................... 37
RAPAMUNE® ........................................................................................................................................... 37

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP
RECOMBIVAX HB® ................................................................................................................................... 37
REMODULIN® .......................................................................................................................................... 37
SANDIMMUNE® ...................................................................................................................................... 37
TACROLIMUS ........................................................................................................................................... 37
TAXOTERE® ............................................................................................................................................. 37
TETANUS DIPHTHERIA TOXOIDS® ........................................................................................................... 37
TETANUS TOXOID ADSORBED ................................................................................................................. 37
TETANUS-DIPHTERIA-DECAVAC® ............................................................................................................ 37
TOBI®....................................................................................................................................................... 37
TOPOSAR ................................................................................................................................................. 37
TOPOTECAN HCL ..................................................................................................................................... 37
TPN ELECTROLYTES® ............................................................................................................................... 37
TRAVASOL® ............................................................................................................................................. 38
TREANDA® ............................................................................................................................................... 38
TRELSTAR® .............................................................................................................................................. 38
TRISENOX® .............................................................................................................................................. 38
TROPHAMINE® ........................................................................................................................................ 38
VANCOMYCIN HCL .................................................................................................................................. 38
VELCADE® ................................................................................................................................................ 38
VIDAZA® .................................................................................................................................................. 38
VINBLASTINE SULFATE ............................................................................................................................ 38
VINCRISTINE SULFATE ............................................................................................................................. 38

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP
VINORELBINE TARTRATE ......................................................................................................................... 38
ZEMPLAR® ............................................................................................................................................... 38
ZOMETA® ................................................................................................................................................ 38
ZORTRESS® .............................................................................................................................................. 38
BANZEL ........................................................................................................................................................ 39
BANZEL® .................................................................................................................................................. 39
BUPRENORPHINE ........................................................................................................................................ 40
BUPRENORPHINE HCL ............................................................................................................................. 40
SUBOXONE® ............................................................................................................................................ 40
BYETTA ........................................................................................................................................................ 41
BYETTA® .................................................................................................................................................. 41
CAMPRAL .................................................................................................................................................... 42
CAMPRAL® .............................................................................................................................................. 42
CAYSTON ..................................................................................................................................................... 43
CAYSTON® ............................................................................................................................................... 43
CEREZYME ................................................................................................................................................... 44
CEREZYME® ............................................................................................................................................. 44
CHANTIX ...................................................................................................................................................... 45
CHANTIX® ................................................................................................................................................ 45
CIMZIA ......................................................................................................................................................... 46
CIMZIA® ................................................................................................................................................... 46
COPAXONE .................................................................................................................................................. 47

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP
COPAXONE® ............................................................................................................................................ 47
DRONABINOL .............................................................................................................................................. 48
DRONABINOL .......................................................................................................................................... 48
ELAPRASE .................................................................................................................................................... 50
ELAPRASE® .............................................................................................................................................. 50
EMSAM........................................................................................................................................................ 51
EMSAM®.................................................................................................................................................. 51
EPLERENONE ............................................................................................................................................... 52
EPLERENONE ........................................................................................................................................... 52
EPO .............................................................................................................................................................. 53
PROCRIT® ................................................................................................................................................ 53
EXJADE ........................................................................................................................................................ 54
EXJADE® .................................................................................................................................................. 54
EXTAVIA....................................................................................................................................................... 55
EXTAVIA®................................................................................................................................................. 55
FABRAZYME ................................................................................................................................................ 56
FABRAZYME® .......................................................................................................................................... 56
FENTANYL PATCH ........................................................................................................................................ 57
FENTANYL................................................................................................................................................ 57
GILENYA ...................................................................................................................................................... 58
GILENYA® ................................................................................................................................................ 58
GLEEVEC ...................................................................................................................................................... 59

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP
GLEEVEC® ................................................................................................................................................ 59
GONADOTROPIN ......................................................................................................................................... 60
CHORIONIC GONADOTROPIN ................................................................................................................. 60
NOVAREL ................................................................................................................................................. 60
PREGNYL®................................................................................................................................................ 60
GROWTH HORMONE .................................................................................................................................. 61
NORDITROPIN FLEXPRO® ........................................................................................................................ 61
NORDITROPIN NORDIFLEX® .................................................................................................................... 61
HEPSERA...................................................................................................................................................... 63
HEPSERA® ................................................................................................................................................ 63
HRM EDITS .................................................................................................................................................. 65
CARISOPRODOL ....................................................................................................................................... 65
CHLORZOXAZONE ................................................................................................................................... 65
CYCLOBENZAPRINE HCL .......................................................................................................................... 65
CYPROHEPTADINE HCL............................................................................................................................ 65
DICYCLOMINE HCL .................................................................................................................................. 65
DIPHENOXYLATE-ATROPINE.................................................................................................................... 65
DIPYRIDAMOLE ....................................................................................................................................... 65
ESTROPIPATE........................................................................................................................................... 65
HYDROXYZINE HCL .................................................................................................................................. 65
HYDROXYZINE PAMOATE ........................................................................................................................ 65
METAXALONE.......................................................................................................................................... 65

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP
METHOCARBAMOL ................................................................................................................................. 65
ORPHENADRINE CITRATE ........................................................................................................................ 65
ORPHENADRINE COMPOUND ................................................................................................................. 65
ORPHENADRINE COMPOUND FORTE ..................................................................................................... 65
ORTHO-EST®............................................................................................................................................ 65
PHENADOZ .............................................................................................................................................. 65
PROMETHAZINE HCL ............................................................................................................................... 65
PROMETHAZINE VC ................................................................................................................................. 65
PROMETHEGAN ...................................................................................................................................... 65
TRANSDERM-SCOP® ................................................................................................................................ 65
TRIMETHOBENZAMIDE HCL .................................................................................................................... 65
HUMIRA....................................................................................................................................................... 67
HUMIRA® ................................................................................................................................................ 67
INCRELEX ..................................................................................................................................................... 69
INCRELEX® ............................................................................................................................................... 69
INFERGEN .................................................................................................................................................... 70
INFERGEN® .............................................................................................................................................. 70
INVEGA SUSTENNA ..................................................................................................................................... 71
INVEGA SUSTENNA® ............................................................................................................................... 71
ITRACONAZOLE ........................................................................................................................................... 72
ITRACONAZOLE ....................................................................................................................................... 72
IVIG .............................................................................................................................................................. 74

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP
GAMMAGARD LIQUID® ........................................................................................................................... 74
GAMUNEX® ............................................................................................................................................. 74
KUVAN......................................................................................................................................................... 76
KUVAN®................................................................................................................................................... 76
LETAIRIS....................................................................................................................................................... 77
LETAIRIS®................................................................................................................................................. 77
LEUKINE....................................................................................................................................................... 78
LEUKINE®................................................................................................................................................. 78
LIDODERM ................................................................................................................................................... 80
LIDODERM®............................................................................................................................................. 80
LUPRON ....................................................................................................................................................... 81
LEUPROLIDE ACETATE ............................................................................................................................. 81
LUPRON DEPOT® ..................................................................................................................................... 81
LUPRON DEPOT-PED® ............................................................................................................................. 81
METHYLPHENIDATES .................................................................................................................................. 83
METADATE ER ......................................................................................................................................... 83
METHYLIN ............................................................................................................................................... 83
METHYLPHENIDATE HCL ......................................................................................................................... 83
METHYLPHENIDATE SR ........................................................................................................................... 83
MOZOBIL ..................................................................................................................................................... 84
MOZOBIL® ............................................................................................................................................... 84
MYOZYME ................................................................................................................................................... 85

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP
MYOZYME® ............................................................................................................................................. 85
NAGLAZYME ................................................................................................................................................ 86
NAGLAZYME® .......................................................................................................................................... 86
NEUPOGEN.................................................................................................................................................. 87
NEUPOGEN®............................................................................................................................................ 87
NEXAVAR ..................................................................................................................................................... 89
NEXAVAR® ............................................................................................................................................... 89
NICOTINE..................................................................................................................................................... 90
NICOTROL NS® ........................................................................................................................................ 90
NICOTROL®.............................................................................................................................................. 90
NUEDEXTA................................................................................................................................................... 91
NUEDEXTA®............................................................................................................................................. 91
NUVIGIL ....................................................................................................................................................... 92
NUVIGIL® ................................................................................................................................................. 92
OCTREOTIDE................................................................................................................................................ 93
OCTREOTIDE ACETATE ............................................................................................................................ 93
ORAL FENTANYL .......................................................................................................................................... 94
FENTANYL CITRATE ................................................................................................................................. 94
ORAL TESTOSTERONES................................................................................................................................ 95
ANDROXY® .............................................................................................................................................. 95
ORFADIN ..................................................................................................................................................... 96
ORFADIN® ............................................................................................................................................... 96

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP
OSTEOPOROSIS ........................................................................................................................................... 97
FORTEO® ................................................................................................................................................. 97
OXSORALEN................................................................................................................................................. 98
OXSORALEN-ULTRA® ............................................................................................................................... 98
PEGASYS ...................................................................................................................................................... 99
PEGASYS® ................................................................................................................................................ 99
PEGINTRON ............................................................................................................................................... 101
PEGINTRON REDIPEN® .......................................................................................................................... 101
PEGINTRON® ......................................................................................................................................... 101
PROMACTA ............................................................................................................................................... 102
PROMACTA® ......................................................................................................................................... 102
RANEXA ..................................................................................................................................................... 104
RANEXA® ............................................................................................................................................... 104
REBIF ......................................................................................................................................................... 105
REBIF® ................................................................................................................................................... 105
RELISTOR ................................................................................................................................................... 106
RELISTOR® ............................................................................................................................................. 106
REMICADE ................................................................................................................................................. 107
REMICADE® ........................................................................................................................................... 107
REVATIO .................................................................................................................................................... 109
REVATIO® .............................................................................................................................................. 109
REVLIMID................................................................................................................................................... 110

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP
REVLIMID® ............................................................................................................................................ 110
RIBAVIRIN .................................................................................................................................................. 112
REBETOL® .............................................................................................................................................. 112
RIBAPAK ................................................................................................................................................ 112
RIBASPHERE .......................................................................................................................................... 112
RIBAVIRIN .............................................................................................................................................. 112
RISPERDAL CONSTA................................................................................................................................... 114
RISPERDAL CONSTA® ............................................................................................................................ 114
RITUXAN .................................................................................................................................................... 115
RITUXAN® .............................................................................................................................................. 115
SABRIL ....................................................................................................................................................... 116
SABRIL® ................................................................................................................................................. 116
SANCUSO................................................................................................................................................... 117
SANCUSO®............................................................................................................................................. 117
SANDOSTATIN LAR .................................................................................................................................... 118
SANDOSTATIN LAR® .............................................................................................................................. 118
SOMATULINE DEPOT................................................................................................................................. 119
SOMATULINE DEPOT®........................................................................................................................... 119
SOMAVERT ................................................................................................................................................ 120
SOMAVERT® .......................................................................................................................................... 120
SPRYCEL ..................................................................................................................................................... 121
SPRYCEL®............................................................................................................................................... 121

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP
STRATTERA ................................................................................................................................................ 122
STRATTERA® .......................................................................................................................................... 122
SUTENT...................................................................................................................................................... 123
SUTENT®................................................................................................................................................ 123
SYMLIN ...................................................................................................................................................... 124
SYMLIN® ................................................................................................................................................ 124
SYMLINPEN 120® .................................................................................................................................. 124
SYMLINPEN 60® .................................................................................................................................... 124
TARCEVA ................................................................................................................................................... 125
TARCEVA® ............................................................................................................................................. 125
TARGRETIN ................................................................................................................................................ 126
TARGRETIN® .......................................................................................................................................... 126
TASIGNA .................................................................................................................................................... 127
TASIGNA® .............................................................................................................................................. 127
TAZORAC ................................................................................................................................................... 128
TAZORAC® ............................................................................................................................................. 128
TESTOSTERONES ....................................................................................................................................... 129
ANDRODERM® ...................................................................................................................................... 129
TESTIM® ................................................................................................................................................ 129
THALOMID................................................................................................................................................. 130
THALOMID®........................................................................................................................................... 130
THIORIDAZINE ........................................................................................................................................... 131

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP
THIORIDAZINE HCL ................................................................................................................................ 131
TOPICAL IMMUNOSUPPRESSANT ............................................................................................................. 132
ELIDEL® .................................................................................................................................................. 132
PROTOPIC® ............................................................................................................................................ 132
TOPICAL-ULCERS ....................................................................................................................................... 133
REGRANEX® ........................................................................................................................................... 133
TRACLEER .................................................................................................................................................. 134
TRACLEER® ............................................................................................................................................ 134
TYKERB ...................................................................................................................................................... 135
TYKERB® ................................................................................................................................................ 135
TYZEKA ...................................................................................................................................................... 136
TYZEKA® ................................................................................................................................................ 136
VIMPAT ..................................................................................................................................................... 138
VIMPAT® ............................................................................................................................................... 138
VOTRIENT .................................................................................................................................................. 139
VOTRIENT® ............................................................................................................................................ 139
VPRIV ......................................................................................................................................................... 140
VPRIV®................................................................................................................................................... 140
XENAZINE .................................................................................................................................................. 141
XENAZINE® ............................................................................................................................................ 141
XIFAXAN .................................................................................................................................................... 142
XIFAXAN® .............................................................................................................................................. 142

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP
XOLAIR....................................................................................................................................................... 143
XOLAIR®................................................................................................................................................. 143
XYREM ....................................................................................................................................................... 144
XYREM® ................................................................................................................................................. 144
ZAVESCA .................................................................................................................................................... 145
ZAVESCA® .............................................................................................................................................. 145
Index.......................................................................................................................................................... 146

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP

ACTEMRA
Affected Drugs
ACTEMRA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Active infection (including TB). Concurrent therapy with other biologic agent(s).
Required Medical Information
Screening for latent tuberculosis is required. If results are positive, patient must have
completed treatment or must currently be receiving treatment for latent tuberculosis.
Evaluate for HBV risk and initiate treatment if appropriate. Must have an inadequate
response or intolerance/contraindication to one TNF [Tumor necrosis factor] antagonist
therapy.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
For renewals, patient must have responded to Actemra therapy (e. g. , condition
improved or stabilized).

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP

ACTIMMUNE
Affected Drugs
ACTIMMUNE®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP

ADAGEN
Affected Drugs
ADAGEN®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Severe thrombocytopenia. Use in preparation for or in support of bone marrow
transplantation.
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
Use for direct replacement for deficient enzyme (no benefit achieved in patients with
immunodeficiency due to other causes).

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP

ADCIRCA
Affected Drugs
ADCIRCA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Nitrate therapy.
Required Medical Information
PAH [Pulmonary Arterial Hypertension] been confirmed by right heart
catheterization.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP

AFINITOR
Affected Drugs
AFINITOR®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
Oncologist.
Coverage Duration
Plan Year.
Other Criteria
N/A

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP

ALDURAZYME
Affected Drugs
ALDURAZYME®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
Diagnosis confirmed by measurement of alpha-L-iduronidase activity (enzymatic
assay) or DNA testing. For Scheie form of MPS I, must have at least 2 moderate to
severe symptoms. Must demonstrate improvement in lung function in patients who have
received at least 26 weeks of Aldurazyme on re-authorization.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP

ALPHA1-PROTEINASE INHIBITOR
Affected Drugs
ARALAST NP®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Patient has IgA deficiency with antibodies against IgA.
Required Medical Information
Alpha1-proteinase inhibitor concentration is less than 11 micromoles per liter. The
FEV1 level is between 35% and 60% predicted OR greater than 60% predicted. If the
FEV1 is greater than 60% predicted, then the patient has experienced a rapid decline in
lung function (ie, reduction of FEV1 more than 120 mL/year) that warrants treatment.
Age Restrictions
18 years old and older.
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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AMPHETAMINES
Affected Drugs
AMPHETAMINE SALT COMBO
DEXTROAMPHETAMINE SULFATE
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
MAOI concurrent use or within the last 14 days except if prescriber is a psychiatrist
with experience prescribing both MAOI and amphetamine/dextroamphetamine drugs.
Required Medical Information
Sleep studies for narcolepsy diagnosis.
Age Restrictions
3 years of age and older.
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
Consider benefits of use versus the potential risks of serious cardiovascular events.

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AMPYRA
Affected Drugs
AMPYRA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Moderate to severe renal impairment (CrCL less than or equal to 50 mL/min), history
of seizures, Ampyra at doses exceeding 10 mg twice daily.
Required Medical Information
Patient must demonstrate sustained walking impairment, but with the ability to walk
25 feet (with or without assistance) prior to starting Ampyra.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
2 months, then plan year upon renewal.
Other Criteria
To continue therapy, the patient must experience an improvement in walking speed
or other objective measure of walking ability since starting Ampyra.

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ANABOLIC STEROIDS
Affected Drugs
ANADROL-50®
OXANDROLONE
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Known or suspected carcinoma of the prostate or breast (in male patients),
carcinoma of the breast in women with hypercalcemia, pregnancy, nephrosis (the
nephrotic phase of nephritis), hypercalcemia.
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
6 months.
Other Criteria
N/A

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GuildNet Gold HMO-POS SNP
GuildNet Health Advantage HMO-POS SNP

ANAGRELIDE
Affected Drugs
ANAGRELIDE HCL
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Severe hepatic impairment.
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
Oncologist or hematologist.
Coverage Duration
6 months.
Other Criteria
N/A

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ARCALYST
Affected Drugs
ARCALYST®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Active or chronic infection. Concurrent therapy with other biologics.
Required Medical Information
N/A
Age Restrictions
12 years of age and older.
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
For renewal, patient's condition must have improved or stabilized.

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ATYPICAL ODT
Affected Drugs
FAZACLO®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
For Fazaclo: a. if the patient has any of the following contraindications:
agranulocytosis, bone marrow suppression, coma, ileus, leukopenia, myocarditis or
neutropenia b. if the patient has CNS depression, dementia-related psychosis or
uncontrolled epilepsy.
Required Medical Information
The patient must be unable/unwilling to take tablets or capsules or are high risk for
non-compliance AND must not be receiving other tablets or capsules indicating that
they can take non-dissolvable tablets.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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GuildNet Health Advantage HMO-POS SNP

AVONEX
Affected Drugs
AVONEX ADMINISTRATION PACK®
AVONEX®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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GuildNet Health Advantage HMO-POS SNP

B VS D - PART B VERSUS PART D COVERAGE PA
Affected Drugs
ACETYLCYSTEINE
ADRIAMYCIN
ALBUTEROL SULFATE
ALIMTA®
AMIFOSTINE
AMINOSYN II 3.5% M-DEXTROSE 5%®
AMINOSYN II 3.5%-DEXTROSE 25%®
AMINOSYN II 3.5%-DEXTROSE 5%®
AMINOSYN II 4.25%-DEXTROSE 25%®
AMINOSYN II 5% IN 25% DEXTROSE®
AMINOSYN II IN DEXTROSE®
AMINOSYN II WITH LYTES-CA-DW®
AMINOSYN II®
AMINOSYN M®
AMINOSYN®
AMINOSYN-HBC®
AMINOSYN-HF®
AMINOSYN-PF®
AMIODARONE HCL
AMPHOTERICIN B
ASTRAMORPH-PF®
AVASTIN®
AZASAN®
AZATHIOPRINE
AZATHIOPRINE SODIUM
BICNU®
BLEOMYCIN SULFATE
BUDESONIDE
BUSULFEX®
CALCITRIOL
CAMPATH®
CARBOPLATIN
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CELLCEPT®
CISPLATIN
CLADRIBINE
CLINIMIX E®
CLINIMIX®
CLINISOL®
COLISTIMETHATE SODIUM
COSMEGEN®
CROMOLYN SODIUM
CUBICIN®
CYCLOPHOSPHAMIDE
CYCLOSPORINE
CYCLOSPORINE MODIFIED
CYTARABINE
DACARBAZINE
DAUNORUBICIN HCL
DEPO-PROVERA®
DEXRAZOXANE
DIPHTHERIA-TETANUS TOXOID®
DOXIL®
DOXORUBICIN HCL
DURAMORPH®
ELITEK®
ELSPAR®
EMEND®
ENGERIX-B®
EPIRUBICIN HCL
ETOPOSIDE
FASLODEX®
FENTANYL CITRATE
FLUDARABINE PHOSPHATE®
FLUOROURACIL
FREAMINE III WITH ELECTROLYTES®
FREAMINE III®
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GAMASTAN S-D®
GANCICLOVIR SODIUM
GEMZAR®
GENGRAF
GRANISETRON HCL
HEPARIN SODIUM
HEPARIN SODIUM IN 0.45% NACL
HEPARIN SODIUM IN 0.9% NACL
HEPARIN SODIUM IN 5% DEXTROSE
HEPATAMINE®
HEPATASOL®
HERCEPTIN®
HYDROMORPHONE HCL
IDARUBICIN HCL
IFEX®
IFOSFAMIDE
IFOSFAMIDE-MESNA
INTRALIPID®
INTRON A®
IPRATROPIUM BROMIDE
IPRATROPIUM-ALBUTEROL
IRINOTECAN HCL
ISTODAX®
LEUCOVORIN CALCIUM
LEVALBUTEROL CONCENTRATE
LEVOCARNITINE
LIPOSYN II®
LIPOSYN III
MELPHALAN HCL
MESNA
METHOTREXATE
MIACALCIN®
MITOMYCIN
MITOXANTRONE HCL
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MORPHINE SULFATE
MUSTARGEN®
MYCOPHENOLATE MOFETIL
MYFORTIC®
NEORAL®
NEPHRAMINE®
NEUMEGA®
ONDANSETRON HCL
ONDANSETRON ODT
ONTAK®
OXALIPLATIN
PACLITAXEL
PENTOSTATIN
PERFOROMIST®
PHOTOFRIN®
PREMASOL®
PROCALAMINE®
PROGRAF®
PROLEUKIN®
PROSOL®
PULMOZYME®
RAPAMUNE®
RECOMBIVAX HB®
REMODULIN®
SANDIMMUNE®
TACROLIMUS
TAXOTERE®
TETANUS DIPHTHERIA TOXOIDS®
TETANUS TOXOID ADSORBED
TETANUS-DIPHTERIA-DECAVAC®
TOBI®
TOPOSAR
TOPOTECAN HCL
TPN ELECTROLYTES®
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TRAVASOL®
TREANDA®
TRELSTAR®
TRISENOX®
TROPHAMINE®
VANCOMYCIN HCL
VELCADE®
VIDAZA®
VINBLASTINE SULFATE
VINCRISTINE SULFATE
VINORELBINE TARTRATE
ZEMPLAR®
ZOMETA®
ZORTRESS®
Covered Uses
This drug may be covered under Medicare Part B or D depending upon the
circumstances. Information may need to be submitted describing the use and setting of
the drug to make the determination.

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BANZEL
Affected Drugs
BANZEL®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
The patient is diagnosed with familial short QT Syndrome.
Required Medical Information
The patient must be diagnosed with seizures associated with Lennox-Gastaut
Syndrome.
Age Restrictions
N/A
Prescriber Restrictions
Neurologist or affiliated with neurology practice.
Coverage Duration
Plan Year.
Other Criteria
N/A

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GuildNet Gold HMO-POS SNP
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BUPRENORPHINE
Affected Drugs
BUPRENORPHINE HCL
SUBOXONE®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Dose in excess of 4 units daily.
Required Medical Information
Documentation that the member is not receiving other opioids.
Age Restrictions
16 years of age and older.
Prescriber Restrictions
Prescribers must be certified through CSAT (The Center for Substance Abuse
Treatment) of SAMHSA (Substance Abuse and Mental Health Services Administration)
to prescribe Suboxone and Subutex.
Coverage Duration
Buprenorphine - one month (12 months if pregnant). Buprenorphine-naloxone - 12
months.
Other Criteria
Buprenorphine and buprenorphine-naloxone should be part of an overall treatment
program. The patient should be monitored periodically.

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BYETTA
Affected Drugs
BYETTA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
History of pancreatitis.
Required Medical Information
A. The patient is diagnosed as having type-2 diabetes with an HbA1c level greater
than 7. B. The patient has a creatinine clearance of greater than 30mL/minute or normal
kidney function. C. The patient has had an inadequate treatment response, intolerance
or contraindication to metformin or a sulfonylurea medication. D. If the patient has
received previous Byetta therapy, the patient demonstrated a reduction in HbA1c since
initiating Byetta therapy.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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CAMPRAL
Affected Drugs
CAMPRAL®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Renal failure.
Required Medical Information
A. Clinical diagnosis for alcohol dependence. B. AND clinical evidence indicated that
the patient will be abstinent at least 5 days prior to treatment initiation. C. AND a trial of
naltrexone (oral/injectable) has been attempted, at clinically significant dosage and
duration. Or therapy is documented to be clinically inappropriate (hepatic insufficiency,
chronic pain medication use). D. AND medication administration should be part of a
comprehensive psychosocial treatment program.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
6 months.
Other Criteria
N/A

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CAYSTON
Affected Drugs
CAYSTON®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
Diagnosis of cystic fibrosis is confirmed by appropriate diagnostic or genetic testing.
Confirmation of P. aeruginosa in cultures of the airways. For continuation of therapy in
patients younger than 6 years of age, a clinical reason to continue therapy, such as
symptomatic improvement, is required. For continuation of therapy in patients older than
6 years of age, pulmonary function tests have not deteriorated more than 10% from
baseline or there is a clinical reason to continue therapy, such as symptomatic
improvement.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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CEREZYME
Affected Drugs
CEREZYME®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Concurrent therapy with Zavesca.
Required Medical Information
Diagnosis confirmed by bone marrow histology, DNA testing, or bglucocerebrosidase enzyme assay (enzyme activity less than 30 percent). Must have at
least one of following conditions: anemia, thrombocytopenia, bone disease,
hepatomegaly, or splenomegaly. Must demonstrate a decrease in liver and spleen
volume and/or increase in platelet count and/or increase in Hgb concentration in
patients who have received at least 24 months of Cerezyme therapy on reauthorization.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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CHANTIX
Affected Drugs
CHANTIX®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Concurrent Zyban use.
Required Medical Information
Evaluation for neuropsychiatric symptoms. If the patient is currently receiving
Chantix, the patient's treatment, including the use of Chantix, has resulted in smoking
cessation.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
12 weeks initial, 12 weeks additional upon renewal.
Other Criteria
Member is participating in a smoking cessation program.

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CIMZIA
Affected Drugs
CIMZIA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Active infection (including TB). Concurrent therapy with other biologics.
Required Medical Information
Screening for latent TB infection and assessment for Hep B risk. For positive latent
TB, patient must have completed treatment or is currently receiving treatment for LTBI.
HBV infection ruled out or treatment initiated for positive infection. Rheumatoid arthritis
(RA) - Must have an inadequate response to either Enbrel or Humira and one of
following: 1) inadequate response to methotrexate, 2) inadequate response to another
nonbiologic DMARD [Disease-modifying antirheumatic drug] (e. g. , leflunomide,
hydroxychloroquine, sulfasalazine) if contraindicated or intolerant to MTX [methotrexate]
or, 3) intolerance or contraindication to at least 2 nonbiologic DMARDs [Diseasemodifying antirheumatic drugs]. Crohn's Disease - Must have an inadequate response
or contraindication/intolerance to at least one oral corticosteroid and Humira.
Age Restrictions
18 years of age and older.
Prescriber Restrictions
N/A
Coverage Duration
Initial: Plan Year for RA [Rheumatoid Arthritis], 3 months for Crohn's disease.
Renewal: Plan Year.
Other Criteria
For re-authorization, patient's condition must have improved or stabilized.
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COPAXONE
Affected Drugs
COPAXONE®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Concurrent use of any of the following medications: Interferon-beta therapy (Avonex,
Betaseron, Extavia, or Rebif), or mitoxantrone.
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
Patients with previous use (12 or more months) of Copaxone must demonstrate one
of the following clinical responses: decrease in the frequency of relapses, slowing of
disease progression, diminished MRI lesions, OR patient is stable on therapy.

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DRONABINOL
Affected Drugs
DRONABINOL
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
A. The diagnosis is documented as anorexia associated with weight loss in a patient
with AIDS a. AND the patient has had an involuntary weight loss of greater than 10% of
pre-illness baseline body weight or a body mass index (BMI) less than 20kg/m2 in the
absence of a concurrent illness or medical condition other than HIV that may cause
weight loss b. AND the patient has failed to respond to a 30-day drug regimen of
megestrol (Megace) c. AND if the patient has received previous dronabinol therapy,
he/she must show a positive response to therapy by maintaining or increasing their
initial weight and/or muscle mass before initiating dronabinol therapy. B. The diagnosis
is documented as nausea and vomiting associated with cancer chemotherapy in a
cancer patient a. AND the patient is receiving a chemotherapy or radiation regimen b.
AND the patient has had a full trial and failure through at least one cycle of
chemotherapy with IV ondansetron AND at least one of the following oral anti-emetic
agents: metoclopramide, promethazine, prochlorperazine, meclizine,
trimethobenzamide, oral 5-HT3 receptor antagonists e. AND if the patient has received
previous dronabinol therapy, he/she must show a positive response by showing a
reduced incidence of emesis and/or nausea.
Age Restrictions
N/A
Prescriber Restrictions
N/A
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Coverage Duration
6 months.
Other Criteria
B vs D coverage determination per CMS guidelines.

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ELAPRASE
Affected Drugs
ELAPRASE®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
Diagnosis confirmed by DNA testing or enzymatic analysis (deficiency of iduronate
2-sulfatase enzyme activity).
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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EMSAM
Affected Drugs
EMSAM®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Pheochromocytoma, concurrent use of the following medications:
dextromethorphan, St. John's Wort.
Required Medical Information
A. Clinical diagnosis of major depressive disorder not responsive other
antidepressants as demonstrated by at least 2 documented trials (clinically sufficient
dose and duration of six weeks or longer) of the following: selective serotonin reuptake
inhibitors (SSRI), serotonin/norepinephrine reuptake inhibitors (SNRI), bupropion,
mirtazapine, or tricyclic/tetracyclic antidepressants B. OR clinical diagnosis of major
depressive disorder for those patients who cannot take any oral preparations (including
commercially available liquid antidepressants). C. For requests over 6 mg/24 hours,
patient must agree to adhere to a tyramine restrictive diet.
Age Restrictions
N/A
Prescriber Restrictions
Psychiatrist or affiliated with a psychiatry practice.
Coverage Duration
Plan Year.
Other Criteria
N/A

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EPLERENONE
Affected Drugs
EPLERENONE
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
A. Diagnosis of hypertension or post-myocardial infarction with LVEF less than or
equal to 40% and clinical evidence of CHF [Congestive Heart Failure] after an acute MI.
B. AND a serum potassium level less than 5. 5 mEq/L. C. For diagnosis of post MI with
LVEF less than or equal to 40% and clinical evidence of CHF [Congestive Heart Failure]
after an acute MI, the patient must meet the following requirement: creatinine clearance
greater than 30 mL/min. D. For the diagnosis of hypertension, the patient must meet the
following requirements: the patient does not have type-2 diabetes with microalbuminuria
AND the patient has a creatinine clearance greater than 50 mL/min AND the patient had
an inadequate treatment response to maximum tolerated doses of a 60-day trial or had
unacceptable toxicity to spironolactone therapy.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A
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EPO
Affected Drugs
PROCRIT®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Uncontrolled hypertension.
Required Medical Information
For use in an anemic patient prior to surgery, the patient must also receive
concomitant iron supplementation. For other indications, all of the following criteria are
required: 1) The pretreatment Hgb is less than or equal to 10 g/dL for initial
authorization. 2) The patient is receiving concomitant iron supplementation if iron stores
are inadequate. 3) The Hgb is maintained at or below 12 g/dL once on therapy. 4) Once
on therapy for 12 weeks, the hemoglobin must increase at least 1 g/dL in response to
epoetin alfa.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
12 weeks.
Other Criteria
N/A

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EXJADE
Affected Drugs
EXJADE®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Creatinine clearance less than 40 mL/min or evidence of overt proteinuria, platelet
count less than 50 x 10(9)/L, advanced malignancy, high-risk myelodysplastic syndrome
(MDS) with poor performance status, or concurrent use of deferoxamine or ironcontaining products.
Required Medical Information
The patient must meet all of the following criteria: 1) Diagnosis of transfusiondependent anemia with chronic iron overload due to blood transfusions, 2) Pretreatment
serum ferritin level within the last 60 days of at least 1, 000 mcg/L, and 3) Patient will
have baseline and monthly monitoring of serum ferritin, serum creatinine, creatinine
clearance, serum transaminases, and bilirubin. For patients already receiving Exjade,
the prescriber will consider temporary interruption of Exjade when serum ferritin is less
than 500 mcg/L.
Age Restrictions
2 years of age and older.
Prescriber Restrictions
Hematologist.
Coverage Duration
3 months.
Other Criteria
N/A
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EXTAVIA
Affected Drugs
EXTAVIA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Concurrent use of any of the following medications: Interferon-beta therapy (Avonex,
Betaseron, or Rebif), glatiramer acetate, or mitoxantrone.
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
Patients with previous use (12 or more months) of Extavia must demonstrate one of
the following clinical responses: decrease in the frequency of relapses, slowing of
disease progression, MRI lesions have diminished with therapy, OR patient is stable on
therapy.

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FABRAZYME
Affected Drugs
FABRAZYME®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
Diagnosis confirmed with an enzyme assay measuring a deficiency of alphagalactosidase enzyme activity or DNA testing.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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FENTANYL PATCH
Affected Drugs
FENTANYL
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Patients who are not opioid tolerant, patients who do not require continuous opioid
analgesia. Patients who are taking any CYP450 3A4 agents who are not being
monitored.
Required Medical Information
Assessment for clinical risk of opioid/substance abuse/addiction through Screener
and Opioid Assessment for Patients with Pain (SOAPP 1. 0), Screener and Opioid
Assessment for Patients with Pain, Revision (SOAPP-R), Opioid Risk Tool (ORT),
Current Opioid Misuse Measure (COMM), The Diagnosis, Intractability, Risk, and
Efficacy Score (DIRE) or other assessment tool.
Age Restrictions
2 years of age and older.
Prescriber Restrictions
N/A
Coverage Duration
6 months.
Other Criteria
N/A

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GILENYA
Affected Drugs
GILENYA®
Covered Uses
All FDA approved uses not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
For new starts, patient had an inadequate response to a trial of a beta interferon
agent or Copaxone unless contraindicated or not tolerated.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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GLEEVEC
Affected Drugs
GLEEVEC®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
Chronic myeloid leukemia (CML) and acute lymphoblastic leukemia (ALL) must be
positive for the Philadelphia chromosome or BCR-ABL gene. For CML [Chronic Myeloid
Leukemia], patient meets one of the following: 1) newly diagnosed, 2) resistance or
intolerance to prior therapy, or 3) recurrence after stem cell transplant. For ALL, patient
meets one of the following: 1) newly diagnosed and Gleevec is used in combination with
chemotherapy, or 2) ALL is relapsed or refractory. For GIST, patient meets one of the
following: 1) unresectable, recurrent, or metastatic disease, or 2) use of Gleevec for
adjuvant therapy following resection, or 3) use of Gleevec for pre-operative therapy and
patient is at risk for significant surgical morbidity.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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GONADOTROPIN
Affected Drugs
CHORIONIC GONADOTROPIN
NOVAREL
PREGNYL®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Female. For prepubertal cryptorchidism, presence of anatomic obstruction or
precocious puberty. For hypogonadotropic hypogonadism, presence of prostatic
carcinoma or other androgen-dependent neoplasm.
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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GROWTH HORMONE
Affected Drugs
NORDITROPIN FLEXPRO®
NORDITROPIN NORDIFLEX®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Active malignancy or history of malignancy in past 12 months, active proliferative or
severe non-proliferative diabetic retinopathy, acute critical illness, concurrent use with
Increlex, and closed epiphyses for pediatric patients. For PWS only: upper airway
obstruction and severe respiratory impairment.
Required Medical Information
For pediatric GHD in neonate with hypoglycemia: patient has a randomly assessed
GH [growth hormone] level less than 20 ng/mL, other causes of hypoglycemia have
been ruled out, and other treatments have been ineffective. For all pediatric patients:
patients have short stature or slow growth velocity and have been evaluated for other
causes of growth failure. For pediatric GHD, patient has delayed bone age. For pediatric
GHD without pituitary disease, patient failed 2 stimulation tests. For pediatric GHD with
a pituitary or CNS disorder, patient has clinical evidence of GHD and low IGF1/IGFBP3. For TS and SHOX patients: diagnosis confirmed by genetic testing. For CRI
patients: metabolic, endocrine and nutritional abnormalities have been treated or
stabilized and patient has not had a kidney transplant. For SGA [Short child born small
for gestational age]: patient has a low birth weight or length for gestational age. For ISS:
pediatric GHD has been ruled out with one stimulation test. For adult GHD, patient was
assessed for other causes of GHD-like symptoms. For adult GHD without pituitary
disease, patient failed 2 stimulation tests. For adult GHD with at least 3 pituitary
hormone deficiencies (PHD) or panhypopituitarism: have a low IGF-1. For adult GHD
with less than 3 PHD, low IGF-1 and failed one stimulation test. For renewal for
pediatric patients, growing more than 2 cm per year and for PWS only: improved body
composition. For renewal for adult patients: patient has seen clinical improvement and
IGF-1 will be monitored.
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Age Restrictions
For Turner syndrome and SGA [Short child born small for gestational age], 2 years
of age and older. For Noonan syndrome and SHOX, 3 years of age and older.
Prescriber Restrictions
Endocrinologist, Pediatric Nephrologist, Gastroenterologist, Nutritional Support
Specialist, Infectious Disease Specialist.
Coverage Duration
Plan Year.
Other Criteria
N/A

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HEPSERA
Affected Drugs
HEPSERA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D, prophylaxis
against HBV infection with liver transplantation.
Exclusion Criteria
Renal impairment without dosing adjustment, if the patient is taking/receiving
tenofovir or PMPA. Use of Hepsera as a first-line therapy in treatment-nave patients
with HBV.
Required Medical Information
A. The patient has been diagnosed with chronic hepatitis B. B. AND the patient has
evidence of a positive HBsAg (+ or -) serological marker for greater than 6 months OR
evidence by a liver biopsy showing chronic hepatitis. C. AND the patient has a Hepatitis
B viral load greater than 20, 000 IU/mL (100, 000 copies per mL) except if for HBeAgnegative HBV, the viral load is greater than 2, 000 IU per mL (10, 000 copies per mL).
D. AND the patient has elevations in liver aminotransferases (ALT or AST) that are two
(2) times greater than normal OR normal liver aminotransferase (ALT or AST) levels
with evidence of significant disease found on biopsy. E. AND the patient is not receiving
Intron A. F. AND documented evidence of diagnosis, serological markers or liver biopsy,
viral load and liver aminotransferases. G. If the patient has received previous Hepsera
treatment, there is documented clinical improvement shown by a drop in viral load or
reduction in the patient's liver aminotransferases.
Age Restrictions
12 years and older.
Prescriber Restrictions
Gastroenterologist or infectious disease specialist or affiliated with an infectious
disease or gastroenterology practice, or a primary care physician with experience in
treating HBV.
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Coverage Duration
Plan Year.
Other Criteria
N/A

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HRM EDITS
Affected Drugs
CARISOPRODOL
CHLORZOXAZONE
CYCLOBENZAPRINE HCL
CYPROHEPTADINE HCL
DICYCLOMINE HCL
DIPHENOXYLATE-ATROPINE
DIPYRIDAMOLE
ESTROPIPATE
HYDROXYZINE HCL
HYDROXYZINE PAMOATE
METAXALONE
METHOCARBAMOL
ORPHENADRINE CITRATE
ORPHENADRINE COMPOUND
ORPHENADRINE COMPOUND FORTE
ORTHO-EST®
PHENADOZ
PROMETHAZINE HCL
PROMETHAZINE VC
PROMETHEGAN
TRANSDERM-SCOP®
TRIMETHOBENZAMIDE HCL
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Not covered for those who are 65 years of age and older.
Required Medical Information
N/A
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Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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HUMIRA
Affected Drugs
HUMIRA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Active infection (including TB), concurrent use with other biologics.
Required Medical Information
Screening for latent TB infection and assessment for Hep B risk. For positive latent
TB, patient must have completed treatment or is currently receiving treatment for LTBI.
HBV infection ruled out or treatment initiated for positive infection. Rheumatoid arthritis Must have one of following: 1) inadequate response to methotrexate (MTX), 2)
inadequate response to another nonbiologic DMARD [Disease-modifying antirheumatic
drug] (e. g. , leflunomide, hydroxychloroquine, sulfasalazine) if contraindicated or
intolerant to MTX [methotrexate], 3) intolerance or contraindication to at least 2
nonbiologic DMARDs [Disease-modifying antirheumatic drugs] or, 4) use Humira as
first-line therapy with MTX [methotrexate] for severely active RA [Rheumatoid Arthritis].
Polyarticular JIA [Juvenile Idiopathic Arthritis] - Must have an inadequate response to at
least one nonbiologic DMARD [Disease-modifying antirheumatic drug] or
intolerance/contraindication to at least 2 nonbiologic DMARDs [Disease-modifying
antirheumatic drugs]. Psoriatic arthritis with predominantly peripheral symptoms - Must
have an inadequate response to at least an 8-week maximum tolerated dose trial of at
least 1 nonbiologic DMARD [Disease-modifying antirheumatic drug] unless
contraindicated or intolerant to such therapy. Psoriatic arthritis with predominantly axial
symptoms and ankylosing spondylitis - Inadequate response or
intolerance/contraindication to at least 2 non-steroidal anti-inflammatory drugs
(NSAIDs). For plaque psoriasis - Must have more than 10% BSA [Body surface area]
affected or has crucial body areas (e. g. , feet, hands, face) affected. Must have an
inadequate response to at least a 60-day trial of 2 conventional therapies (e. g. ,
phototherapy, calcipotriene, MTX [methotrexate], acitretin) unless contraindicated or
intolerant to such therapies. Crohn's disease - Must have an inadequate response to at
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least a 60-day trial of 2 conventional therapies (e. g. , sulfasalazine, mesalamine,
azathioprine, corticosteroids) unless contraindicated or intolerant to such therapies OR
an inadequate response or intolerance to either Remicade or Cimzia.
Age Restrictions
For psoriasis, patient must be 18 years of age and older.
Prescriber Restrictions
N/A
Coverage Duration
Initial: 3 months for Crohn's disease and plan year for all other indications Renewal:
Plan Year.
Other Criteria
For re-authorization, patient's condition must have improved or stabilized.

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INCRELEX
Affected Drugs
INCRELEX®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Epiphyseal closure, IV administration of Increlex, active malignancy, use in
neonates, concurrent use with GH [growth hormone] therapy, patient has secondary
causes of IGF-1 deficiency.
Required Medical Information
Prior to starting therapy, a height greater than 3 SD below the mean for
chronological age and sex, and an IGF-1 level greater than or equal to 3 SD below the
mean for chronological age and gender. One stimulation test showing patient has a
normal or elevated GH [growth hormone] level. For continuation of therapy, patient grew
more than 2. 5 cm/year.
Age Restrictions
Between 2 and 20 years of age.
Prescriber Restrictions
Endocrinologist.
Coverage Duration
Plan Year.
Other Criteria
N/A

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INFERGEN
Affected Drugs
INFERGEN®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Decompensated liver disease. Autoimmune hepatitis.
Required Medical Information
Prior to initiating therapy, detectable levels of HCV RNA in the serum. For treatment
nave, patient must have tried and had intolerance to pegylated interferon based
treatment regimen. Allow Infergen monotherapy for treatment nave if patient has a
contraindication or intolerance to ribavirin. For retreatment, must use in combination
with ribavirin and must have tried and failed to respond to pegylated interferon and
ribavirin. Allow only one time for retreatment. For Genotype 1 and 4: undetectable HCV
RNA after 12 weeks of treatment OR at least 2 log decrease in HCV RNA after 12
weeks of therapy and undetectable HCV RNA after 24 weeks of treatment.
Age Restrictions
N/A
Prescriber Restrictions
ID specialist, gastroenterologist, or oncologist.
Coverage Duration
12 weeks to a total of 72 weeks depending on genotype and initial vs. renewal
therapy.
Other Criteria
Monitored for evidence of depression.

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INVEGA SUSTENNA
Affected Drugs
INVEGA SUSTENNA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Treatment of patients with dementia-related psychosis, patients with occurrence of
torsade de pointes, prior use of risperidone demonstrated a hypersensitivity reaction.
Required Medical Information
A. Diagnosis is an FDA-approved indication: acute and maintenance treatment of
schizophrenia in adults. B. AND the diagnosis is NOT documented as dementia-related
psychosis. C. AND Invega Sustenna therapy will not be used if prior use of risperidone
demonstrated a hypersensitivity reaction D. AND the patient has a history of noncompliance and/or refuses to utilize oral medication E. AND the patient has received at
least ONE of the following: a. three test doses of risperidone b. three test doses of oral
Invega c. previous use of Invega Sustenna. F. If the patient in increasing the dose of
Invega Sustenna, the patient must have a history of two prior injections.
Age Restrictions
N/A
Prescriber Restrictions
Psychiatrist or receiving input from a psychiatry practice.
Coverage Duration
Plan Year.
Other Criteria
N/A

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ITRACONAZOLE
Affected Drugs
ITRACONAZOLE
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
A. ventricular dysfunction (e. g. , congestive heart failure (CHF) or history of CHF
[Congestive Heart Failure]) do not use for onychomycosis. B. If the patient is
taking/receiving any of the following: concomitant use with drugs metabolized by
CYP3A4 (e. g. , cisapride, dofetilide, pimozide, quinidine).
Required Medical Information
Patients with a diagnosis of blastomycosis, pulmonary or extrapulmonary OR
patients with a diagnosis of histoplasmosis, including chronic cavitary pulmonary
disease or disseminated, non-meningeal histoplasmosis OR patients with a diagnosis of
aspergillosis, pulmonary or extrapulmonary OR patients with a diagnosis of
onychomycosis of the toenail, with or without fingernail involvement, due to
dermatophytes (tinea unguium) OR patients with a diagnosis of onychomycosis of the
fingernail due to dermatophytes (tinea unguium). For onychomycosis, diagnosis has
been confirmed with a fungal diagnostic test (e. g. , KOH preparation, fungal culture, or
nail biopsy).
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
12 weeks.

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Other Criteria
N/A

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IVIG
Affected Drugs
GAMMAGARD LIQUID®
GAMUNEX®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
IgA deficiency with antibody formation and a history of hypersensitivity. History of
anaphylaxis or severe systemic reaction to human immune globulin. Presence of risk
factor(s) for acute renal failure, unless the patient will receive IGIV products at the
minimum concentration available and at the minimum rate of infusion practicable OR
Gamunex/Gamunex-C is administered SC for PID.
Required Medical Information
Serum trough and IgG levels below 600, platlet counts, CD4 counts and
lymphocyte counts. Chart notes of past illness and for multiple myeloma, any infections
in the past year. Evidence of positive GMI antibodies

Age Restrictions
N/A
Prescriber Restrictions
CIDP diagnosis by a neurologist.
Coverage Duration
Plan Year.

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Other Criteria
Gamunex/Gamunex-C: if administered SC outside of a controlled healthcare setting,
appropriate treatment (eg, anaphylaxis kit) should be available for managing an acute
hypersensitivity reaction.

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KUVAN
Affected Drugs
KUVAN®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
Blood phenylalanine (Phe) levels. Pretreatment blood phenylalanine (Phe) levels
greater than 10mg/dL if the patient is older than 12 years of age or greater than 6mg/dL
if less than or equal to 12 years of age. Response to a therapeutic trial (greater than or
equal to a 30% reduction in blood Phe levels) is required for long-term authorization.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
1 month initial, plan year on renewal.
Other Criteria
Blood Phe levels should be checked after 1 week of therapy and periodically up to
one month during a therapeutic trial.

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LETAIRIS
Affected Drugs
LETAIRIS®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Pregnancy.
Required Medical Information
NYHA class II or III symptoms. PAH [Pulmonary Arterial Hypertension] been
confirmed by right heart catheterization.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
UD or two appropriate contraceptive methods will be used for women of childbearing
potential.

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LEUKINE
Affected Drugs
LEUKINE®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Administration within 24 hours preceding or following chemotherapy or radiotherapy,
hypersensitivity to yeast-derived products. For prophylaxis of febrile neutropenia: use to
increase the chemotherapy dose intensity or dose schedule above established
regimens. For treatment of febrile neutropenia, when patient receives Neulasta during
the current chemotherapy cycle. For AML [Acute Myeloid Lymphoma] only, excessive
(greater than or equal to 10%) leukemic myeloid blasts in the bone marrow or peripheral
blood.
Required Medical Information
For patients with nonmyeloid malignancies receiving myelosuppressive
chemotherapy: Leukine may be used for the prevention of chemotherapy-induced
febrile neutropenia if the patient experienced febrile neutropenia with a prior
chemotherapy cycle OR the patient is at high risk (greater than 20%) or intermediate
risk (10-20%) for developing febrile neutropenia. Patients at low risk (less than 10%) for
developing febrile neutropenia may also receive Leukine for prophylaxis if there is a
significant risk for serious medical consequences due to febrile neutropenia and the
intent of chemotherapy is to prolong survival or cure the disease. Leukine is allowable
for the treatment of febrile neutropenia in patients who have received prophylaxis with
Leukine (or Neupogen) OR in patients at risk for infection-related complications. All
patients must receive baseline and regular monitoring of complete blood counts and
platelet counts.
Age Restrictions
N/A

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Prescriber Restrictions
N/A
Coverage Duration
6 months.
Other Criteria
N/A

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LIDODERM
Affected Drugs
LIDODERM®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Patient has a sensitivity to local anesthetics of the amide type (e. g. , procaine,
tetracaine, benzocaine. Dose in excess of 3 patches per day.
Required Medical Information
A. The diagnosis is documented as post-herpetic neuralgia B. The skin where the
patch is to be applied is intact (not broken or inflamed). C. The patient has completed a
documented one month trial and failure of the following two medications: gabapentin
OR Lyrica D. OR the patient has a contraindication or demonstrated an adverse event
to the prerequisite drugs.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
3 months.
Other Criteria
N/A

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LUPRON
Affected Drugs
LEUPROLIDE ACETATE
LUPRON DEPOT®
LUPRON DEPOT-PED®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Pregnancy and breast feeding in female patients of childbearing potential For
prostate cancer, use as neoadjuvant androgen deprivation therapy (ADT) for radical
prostatectomy For endometriosis and fibroids, undiagnosed abnormal vaginal bleeding.
Required Medical Information
For prostate cancer: 1) allow therapy for locally advanced, recurrent or metastatic
disease, 2) allow initial long-term neoadjuvant/concurrent/adjuvant ADT in combination
with radiation therapy for clinically localized disease with high risk of recurrence, 3)
allow initial short-term neoadjuvant/concurrent/adjuvant ADT in combination with
radiation therapy for clinically localized disease with intermediate risk of recurrence or
with brachytherapy for clinically localized disease with high risk of recurrence, or 4)
allow neoadjuvant therapy in conjunction with brachytherapy in patients with a large
prostate to shrink the prostate to an acceptable size for brachytherapy For
endometriosis: patient must have completed a trial and failure of at least 2 of the
following therapies: oral contraceptives, medroxyprogesterone, or danazol.
Age Restrictions
For CPP, patient must be less than 12 years old if female and less than 13 years old
if male.
Prescriber Restrictions
N/A

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Coverage Duration
Prostate CA: 1 year but 6 months for short term use, Fibroids: 3 months,
Endometriosis: 6 months, CPP: 1 year.
Other Criteria
N/A

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METHYLPHENIDATES
Affected Drugs
METADATE ER
METHYLIN
METHYLPHENIDATE HCL
METHYLPHENIDATE SR
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
MAOI concurrent use or within the last 14 days.
Required Medical Information
Sleep studies for narcolepsy diagnosis.
Age Restrictions
6 years of age and older.
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
Consider benefits of use versus the potential risks of serious cardiovascular events.

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MOZOBIL
Affected Drugs
MOZOBIL®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
6 months.
Other Criteria
Mozobil is given in combination with granulocyte-colony stimulating factor.

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MYOZYME
Affected Drugs
MYOZYME®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
Diagnosis confirmed by DNA testing or an enzymatic assay showing a deficiency in
acid alpha glucosidase.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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NAGLAZYME
Affected Drugs
NAGLAZYME®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
Diagnosis confirmed by DNA testing or an enzymatic assay showing a deficiency in
N-acetylgalactosamine activity. Patient must have at least one MPS VI symptom. For
re-authorization of Naglazyme, patient must demonstrate improvement in walking
and/or stair-climbing capacity.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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NEUPOGEN
Affected Drugs
NEUPOGEN®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Administration within 24 hours preceding or following chemotherapy or radiotherapy,
E coli hypersensitivity. For prophylaxis of febrile neutropenia: use to increase the
chemotherapy dose intensity or dose schedule beyond established regimen. For
treatment of febrile neutropenia, when patient receives Neulasta during the current
chemotherapy cycle.
Required Medical Information
For patients with nonmyeloid malignancies receiving myelosuppressive
chemotherapy: Neupogen may be used for the prevention of chemotherapy-induced
febrile neutropenia if the patient experienced febrile neutropenia with a prior
chemotherapy cycle OR the patient is at high risk (greater than 20%) or intermediate
risk (10-20%) for developing febrile neutropenia. Patients at low risk (less than 10%) for
developing febrile neutropenia may receive Neupogen for prophylaxis if there is a
significant risk for serious medical consequences due to febrile neutropenia and the
intent of chemotherapy is to prolong survival or cure the disease. Neupogen is allowable
for the treatment of febrile neutropenia in patients who have received prophylaxis with
Neupogen (or Leukine) OR in patients at risk for infection-related complications. All
patients must receive baseline and regular monitoring of complete blood counts and
platelet counts.
Age Restrictions
N/A
Prescriber Restrictions
N/A
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Coverage Duration
6 months.
Other Criteria
N/A

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NEXAVAR
Affected Drugs
NEXAVAR®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Combination with carboplatin and paclitaxel in patients with squamous cell lung
cancer.
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
Oncologist.
Coverage Duration
Plan Year.
Other Criteria
N/A

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NICOTINE
Affected Drugs
NICOTROL NS®
NICOTROL®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
Documentation that the patient is enrolled in a smoking cessation program.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
6 months.
Other Criteria
N/A

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NUEDEXTA
Affected Drugs
NUEDEXTA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Concomitantly taking other drugs containing quinidine, quinine, mefloquine,
monoamine oxidase inhibitors (MAOIs), or drugs that both prolong QT interval and are
metabolized by CYP2D6 (e. g. , thioridazine and pimozide), patient has a prolonged QT
interval, congenital long QT syndrome or a history suggestive of torsades de pointes, or
heart failure, patient has complete atrioventricular (AV) block without implanted
pacemaker, or is at high risk of complete AV block. Dose in excess of 2 capsules per
day.
Required Medical Information
Patient has amyotrophic lateral sclerosis (ALS) OR multiple sclerosis (MS).
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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NUVIGIL
Affected Drugs
NUVIGIL®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
If diagnosis is narcolepsy require Sleep Lab Evaluation, if diagnosis of OSAHS
[Obstructive sleep apnea/hypoapnea syndrome] require polysomnography and whether
the patient is using CPAP [Continuous positive airway pressure] or CPAP [Continuous
positive airway pressure] is contraindicated or ineffective. If diagnosis of Shift Work
Sleep Disorder (work the night shift (at least 6 hours between the hours of 10pm and
8am permanently or work the night shift (at least 6 hours between the hours of 10pm
and 8am) frequently (5 times or more per month) AND experience excessive sleepiness
while working. If diagnosis of mild obstructive sleep apnea/hypopnea syndrome and
whether patient is using and compliant with an oral appliance.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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OCTREOTIDE
Affected Drugs
OCTREOTIDE ACETATE
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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ORAL FENTANYL
Affected Drugs
FENTANYL CITRATE
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Patients taking strong or moderate cytochrome P450 3A4 inhibitor(s) (e. g. ,
aprepitant, clarithromycin, diltiazem, erythromycin, fosamprenavir, fluconazole,
itraconazole, ketoconazole, nefazodone, nelfinavir, ritonavir, verapamil) who will not be
monitored or have dosing adjustments made if necessary.
Required Medical Information
N/A
Age Restrictions
16 years of age and older (Actiq), 18 years of age and older all others.
Prescriber Restrictions
N/A
Coverage Duration
6 months.
Other Criteria
N/A

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ORAL TESTOSTERONES
Affected Drugs
ANDROXY®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Male patients who have confirmed or suspected carcinoma of the prostate or breast.
Required Medical Information
For female patients being treated for inoperable metastatic breast cancer who are 1
to 5 years postmenopausal (either naturally or surgically) and who have had an
incomplete response to other therapies for metastatic breast cancer. For male patients
being treated for primary or secondary hypogonadism, a confirmed low testosterone
level (morning total testosterone less than 300 ng/dL, morning free or bioavailable
testosterone less than 5 ng/dL) or absence of endogenous testosterone. For male
patients being treated for delayed puberty, bone development must be checked at least
every 6 months.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
Patients who have tried and failed or unable to tolerate non-oral forms of
testosterone supplementation.

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ORFADIN
Affected Drugs
ORFADIN®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
Confirmation of diagnosis by either biochemical testing (e. g. , detection of
succinylacetone in urine) and appropriate clinical picture OR DNA testing (mutation
analysis).
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
Protein-restricted diet that is low in phenylalanine and tyrosine.

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OSTEOPOROSIS
Affected Drugs
FORTEO®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Paget's disease of bone, unexplained elevations in alkaline phosphatase, open
epiphyses, prior radiation therapy involving the skeleton, history of a skeletal
malignancy or bone metastases, pre-existing hypercalcemia, metabolic bone disease
other than osteoporosis, concurrent bisphosphonate use, or cumulative use of Forteo
for more than 24 months lifetime.
Required Medical Information
Patient meets one of the following criteria: 1) Patient has experienced a prior fragility
fracture, or 2) Patient had an inadequate response to an adequate trial of a
bisphosphonate (one year) or patient has a contraindication or intolerance to
bisphosphonate trial, or 3) Patient has 2 of the following risk factors for fracture:
advanced age, parental history of fracture, low body mass index, current smoker,
chronic alcohol use, rheumatoid arthritis, chronic steroid use, or other secondary cause
of osteoporosis.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A
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OXSORALEN
Affected Drugs
OXSORALEN-ULTRA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
The patient must be diagnosed with cutaneous T-cell lymphoma OR psoriasis AND if
the diagnosis is psoriasis, the patient must have previous must have previous
inadequate treatment response or intolerance or contraindication to at least one topical
steroid.
Age Restrictions
N/A
Prescriber Restrictions
Dermatologist or Oncologist or affiliated with a dermatologist/oncologist practice.
Coverage Duration
Plan Year.
Other Criteria
N/A

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PEGASYS
Affected Drugs
PEGASYS®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Decompensated liver disease. Autoimmune hepatitis. Concomitant administration of
didanosine with ribavirin in patients coinfected with HIV.
Required Medical Information
HCV: Prior to initiating therapy, detectable levels of HCV RNA in the serum. For
HCV treatment nave, allow Pegasys monotherapy if patient has a contraindication or
intolerance to ribavirin. For HCV retreatment, must use in combination with ribavirin and
must have nonresponse or relapse with prior HCV therapy. Allow only one time for
retreatment with pegylated interferon and ribavirin. For Genotype 1 and 4: undetectable
HCV RNA after 12 weeks of treatment OR at least 2 log decrease in HCV RNA after 12
weeks of therapy and undetectable HCV RNA after 24 weeks of treatment. HBV: Must
have been HBsAg positive for at least 6 months and have persistent or intermittently
elevated ALT greater than 2x ULN or liver biopsy showing chronic hepatitis with
moderate to severe necroinflammation. For HBeAg positive, must have serum HBVDNA greater than 100, 000 copies/mL or greater than 20, 000 IU/mL. For HBeAg
negative, must have serum HBV-DNA greater than 10, 000 copies/mL or greater than 2,
000 IU/mL.
Age Restrictions
N/A
Prescriber Restrictions
ID specialist, Gastroenterologist, Oncologist.

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Coverage Duration
HCV:12 weeks to 72 weeks total depending on genotype and initial vs. renewal
therapy. HBV:48 weeks.
Other Criteria
Monitor for evidence of depression.

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PEGINTRON
Affected Drugs
PEGINTRON REDIPEN®
PEGINTRON®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Decompensated liver disease. Autoimmune hepatitis. Concomitant administration of
didanosine with ribavirin in patients coinfected with HIV.
Required Medical Information
HCV: Prior to initiating therapy, detectable levels of HCV RNA in the serum. For
HCV treatment nave, allow PegIntron monotherapy if patient has a contraindication or
intolerance to ribavirin. For retreatment, must use in combination with ribavirin and must
have nonresponse or relapse with prior HCV therapy. Allow only one time for
retreatment with pegylated interferon and ribavirin. For Genotype 1 and 4: undetectable
HCV RNA after 12 weeks of treatment OR at least 2 log decrease in HCV RNA after 12
weeks of therapy and undetectable HCV RNA after 24 weeks of treatment.
Age Restrictions
N/A
Prescriber Restrictions
ID specialist, Gastroenterologist, Oncologist.
Coverage Duration
12 weeks to a total 72 weeks depending on genotype and initial vs. renewal therapy.
Other Criteria
Monitor for evidence of depression.

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PROMACTA
Affected Drugs
PROMACTA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
For new starts, at the time of diagnosis of ITP [Immune thrombocytopenic purpura]
one of the following are required: 1) a pretreatment platelet count less than 30,
000/microL or 2) a platelet count less than or equal to 50, 000/microL with significant
mucous membrane bleeding or risk factors for bleeding. Patients must be evaluated for
other causes of thrombocytopenia and have had an insufficient response or intolerance
to corticosteroids, or immunoglobulins, or splenectomy. For continuation of therapy, one
of the following are required: 1) an increase in platelet count to greater than or equal to
50, 000/microL or 2) an increase in platelet level that is sufficient to avoid clinically
important bleeding after at least 4 weeks of Promacta at the maximum dose. For all
patients receiving Promacta therapy, if platelets increase above 200, 000/microL,
therapy will be adjusted to maintain the minimal platelet count needed to reduce the risk
for bleeding. Liver function must be assessed pretreatment and regularly throughout
therapy. To continue Promacta therapy, alanine aminotransferase levels must not be
greater than or equal to 3 times the upper limit of normal with any of the following
characteristics: progressive, persistent, accompanied by increased bilirubin or
symptoms of liver injury or evidence of hepatic decompensation.
Age Restrictions
N/A
Prescriber Restrictions
N/A
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Coverage Duration
6 month initial, 12 month renewal if adequate platelet response, 3 month w/o platelet
response.
Other Criteria
N/A

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RANEXA
Affected Drugs
RANEXA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Patients with clinically significant hepatic impairment.
Required Medical Information
A. The diagnosis documented as chronic angina with symptoms limiting daily
activities. B. AND the patient is NOT receiving a medication that prolongs the QT
interval C. AND the patient has tried, failed and/or been intolerant (continues to have
angina symptoms that limits daily activities) to a 30-day trial of the following: with a
nitrate plus a beta blocker OR a calcium channel blocker. D. AND if the patient has
received prior treatment with Ranexa, the patient must experience a decrease in angina
frequency since initiating treatment.
Age Restrictions
N/A
Prescriber Restrictions
Cardiologist or affiliated with a cardiology practice.
Coverage Duration
3 months initial, 12 months renewal.
Other Criteria
N/A

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REBIF
Affected Drugs
REBIF®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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RELISTOR
Affected Drugs
RELISTOR®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Mechanical gastrointestinal obstruction, known or suspected.
Required Medical Information
A. Relistor is being prescribed for treatment of opioid-induced constipation in
patients with advanced illness who are receiving palliative care. B. patient must have
previous trial/failure of polyethylene glycol.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
4 Months.
Other Criteria
N/A

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REMICADE
Affected Drugs
REMICADE®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Active infection (including TB), concurrent use with other biologics, unstable
moderate to severe HF (NYHA Functional Class III/IV).
Required Medical Information
Screening for latent TB infection and assessment for Hep B risk. For positive latent
TB, patient must have completed treatment or is currently receiving treatment for LTBI.
HBV infection ruled out or treatment initiated for positive infection. Rheumatoid arthritis An inadequate response or intolerance to Enbrel or Humira and one of the following: 1)
inadequate response to methotrexate (MTX), 2) inadequate response to another
nonbiologic DMARD [Disease-modifying antirheumatic drug] (e. g. , leflunomide,
hydroxychloroquine, sulfasalazine) if contraindicated or intolerant to MTX
[methotrexate], 3) intolerance or contraindication to at least 2 nonbiologic DMARDs
[Disease-modifying antirheumatic drugs]. Psoriatic arthritis with predominantly
peripheral symptoms - Must meet both of the following: 1) have an inadequate response
or intolerance to either Enbrel or Humira, and 2) have an inadequate response to at
least an 8-week maximum tolerated dose trial of at least 1 nonbiologic DMARD
[Disease-modifying antirheumatic drug] unless contraindicated or intolerant to such
therapy. Psoriatic arthritis with predominantly axial symptoms and ankylosing spondylitis
- Must have an inadequate response or intolerance/contraindication to at least 2 nonsteroidal anti-inflammatory drugs (NSAIDs). For plaque psoriasis - More than 10% BSA
[Body surface area] affected or has crucial body areas (e. g. , feet, hands, face)
affected. An inadequate response to at least a 60-day trial of 2 conventional therapies
(e. g. , phototherapy, calcipotriene, MTX [methotrexate], acitretin) unless
contraindicated or intolerant to such therapies. Crohn's disease - Must meet both of the
following: 1) have an inadequate response to at least a 60-day trial of 1 conventional
therapy (e. g. , corticosteroids, sulfasalazine, azathioprine, mesalamine) unless
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contraindicated or intolerant to such therapy, and 2) have an inadequate response or
intolerance to either Humira or Cimzia. Ulcerative colitis - An inadequate response to at
least a 60-day trial of 2 conventional therapies (e. g. , corticosteroids, mesalamine)
unless contraindicated or intolerant to such therapies.
Age Restrictions
For plaque psoriasis, patient must be 18 years of age and older.
Prescriber Restrictions
N/A
Coverage Duration
Initial: 3 months for Crohn's disease and UC [Ulcerative colitis], plan year for all
others. Renewal: plan year.
Other Criteria
For continuation of therapy, patient's condition must have improved or stabilized.

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REVATIO
Affected Drugs
REVATIO®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Nitrate therapy.
Required Medical Information
Diagnosis of pulmonary arterial hypertension (PAH), (WHO Group 1). PAH
[Pulmonary Arterial Hypertension] been confirmed by right heart catheterization. If
patient is an infant, PAH [Pulmonary Arterial Hypertension] diagnosed by Doppler
echocardiogram. The patient has had an inadequate response or intolerance to Adcirca.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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REVLIMID
Affected Drugs
REVLIMID®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Pregnancy.
Required Medical Information
For active myeloma, patient meets one of the following: 1) Revlimid is used after at
least one prior therapy or as salvage therapy. 2) Revlimid is used with dexamethasone
as primary induction therapy or in combination with melphalan and prednisone in
nontransplant candidates. 3) Revlimid is used as maintenance monotherapy following
response to either stem cell transplant or primary induction therapy. For Low or
Intermediate-1 Risk myelodysplastic syndrome (MDS): for those with 5q deletion,
patients should have transfusion-dependent anemia or symptomatic anemia with
clinically significant cytopenias. For those with non-5q deletion MDS [Myelodysplastic
syndrome] and symptomatic anemia, patients should have failed to respond to epoetin
alfa or darbepoetin or have a pretreatment serum erythropoietin levels greater than 500
mU/mL and a low probability of response to immunosuppressive therapy. For female
patients of childbearing potential, pregnancy is excluded by 2 negative serum or urine
pregnancy tests. For all patients, complete blood counts are monitored for hematologic
toxicity while receiving Revlimid.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
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Other Criteria
Male and female patients of child-bearing potential should be instructed on the
importance of proper utilization of appropriate contraceptive methods for Revlimid use.
Patients should be monitored for signs and symptoms of thromboembolism.

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RIBAVIRIN
Affected Drugs
REBETOL®
RIBAPAK
RIBASPHERE
RIBAVIRIN
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Hemoglobin less than 8. 5 g/dL. Hemoglobinopathy. History of unstable heart
disease. Creatinine clearance less than 50 mL/minute and unwilling to use modified
dose of ribavirin. Pregnancy (self or partner). Unwilling to use effective contraception.
Coadministration with didanosine in HIV coinfected patients.
Required Medical Information
Prior to initiating therapy, detectable levels of HCV RNA in the serum. Must use in
combination with interferon. For retreatment: patient must have nonresponse or relapse
with prior HCV therapy. Allow only one time retreatment with pegylated interferon and
ribavirin OR Infergen and ribavirin. For Genotype 1 and 4: undetectable HCV RNA after
12 weeks of treatment OR at least 2 log decrease in HCV RNA after 12 weeks of
therapy and undetectable HCV RNA after 24 weeks of treatment.
Age Restrictions
N/A
Prescriber Restrictions
ID specialist, gastroenterologist, or oncologist.
Coverage Duration
12 weeks to a total 72 weeks depending on genotype and initial vs. renewal therapy.

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Other Criteria
Patient has been instructed to practice effective contraception during therapy and for
six months after stopping ribavirin therapy.

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RISPERDAL CONSTA
Affected Drugs
RISPERDAL CONSTA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Dementia-related psychosis.
Required Medical Information
A. The patient has a history of non-compliance or refuses to utilize oral medications.
B. The patient must have history of 3 test doses of oral risperidone. C. If the patient is
increasing the dose of Risperdal Consta they must have a history of two prior injections.
Age Restrictions
N/A
Prescriber Restrictions
Psychiatrist or receiving input from psychiatry practice.
Coverage Duration
Plan Year.
Other Criteria
N/A

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RITUXAN
Affected Drugs
RITUXAN®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
History of severe skin or infusion reaction with Rituxan that cannot be appropriately
managed, use in combination with another biologic agent.
Required Medical Information
Chart notes showing pharmacological treatments and the severity of rheumatoid
arthritis must be moderate to severe. Evidence of Methotrexate treatment and
inadequate response to 1 or more TNF antagonist

Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
Monitored for pulmonary toxicity.

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SABRIL
Affected Drugs
SABRIL®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Patients with or at high risk of vision loss (except patients who have blindness).
Patients using other medications associated with serious adverse ophthalmic effects
such as retinopathy or glaucoma.
Required Medical Information
Vision is assessed at baseline or will be assessed by an ophthalmologist no longer
than 4 weeks after starting Sabril (except patients who have blindness). For
continuation of therapy, patient's vision will be assessed by an ophthalmologist every 3
months (except for patients who have blindness). For complex partial seizures (CPS),
the patient has failed an adequate regimen with either carbamazepine or phenytoin,
unless there is a contraindication or intolerance.
Age Restrictions
Initial treatment infantile spasms, 1 month to 2 years. Initial treatment CPS, 16 years
or older.
Prescriber Restrictions
N/A
Coverage Duration
Infantile spasms: initial 4 weeks, reauth 6 months. CPS: initial 3 months, reauth 12
months.
Other Criteria
For continuation of therapy, patient has shown substantial clinical benefit from Sabril
therapy.
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SANCUSO
Affected Drugs
SANCUSO®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
Documentation showing that the patient has had a previous trial/failure to any oral
therapy.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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SANDOSTATIN LAR
Affected Drugs
SANDOSTATIN LAR®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
Patient received initial treatment with Sandostatin Injection (not the Depot form) for
at least 2 weeks and treatment with Sandostatin Injection was effective and tolerable.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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SOMATULINE DEPOT
Affected Drugs
SOMATULINE DEPOT®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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SOMAVERT
Affected Drugs
SOMAVERT®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
IV administration of Somavert, concomitant use of Sandostatin or Somatuline.
Required Medical Information
Diagnosis of acromegaly was confirmed by an elevated IGF-1 level or elevated GH
[growth hormone] level with a glucose tolerance test. Patient has tried and failed at least
a 3 month trial of Sandostatin or Somatuline. For renewal, reduction in IGF-1 level from
baseline.
Age Restrictions
N/A
Prescriber Restrictions
Endocrinologist.
Coverage Duration
Plan Year.
Other Criteria
N/A

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SPRYCEL
Affected Drugs
SPRYCEL®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
Acute lymphoblastic leukemia (ALL) and newly diagnosed chronic myeloid leukemia
(CML) must be positive for the Philadelphia chromosome or BCR-ABL gene. For CML
[Chronic Myeloid Leukemia], patient meets one of the following: 1) newly diagnosed in
chronic phase, 2) resistance or intolerance to imatinib, or 3) relapse after stem cell
transplant. For ALL, patient meets one of the following: 1) ALL is newly diagnosed and
Sprycel is used in combination with chemotherapy, or 2) resistance or intolerance to
prior therapy.
Age Restrictions
18 years of age and older.
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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STRATTERA
Affected Drugs
STRATTERA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
MAOI concurrent use or within the last 14 days.
Required Medical Information
N/A
Age Restrictions
6 years of age and older.
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
Monitor for suicidality, clinical worsening, changes in behavior, blood pressure
changes, heart rate changes, liver injury.

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SUTENT
Affected Drugs
SUTENT®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Clinical manifestations of congestive heart failure.
Required Medical Information
For gastrointestinal stromal tumor (GIST), disease progression while on an at least
30-day regimen of Gleevec or intolerance to Gleevec is required. LFT monitoring at
initiation of therapy and throughout treatment.
Age Restrictions
N/A
Prescriber Restrictions
Oncologist.
Coverage Duration
Plan Year.
Other Criteria
Therapy will be interrupted for serious hepatic adverse events and discontinued if
serious hepatic adverse events do not resolve.

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SYMLIN
Affected Drugs
SYMLIN®
SYMLINPEN 120®
SYMLINPEN 60®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Severe hypoglycemia that required assistance during the past 6 months,
gastroparesis, patient requires drug therapy to stimulate gastrointestinal motility, the
presence of hypoglycemia unawareness (i. e. , inability to detect and act upon the signs
or symptoms of hypoglycemia).
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
The patient must have inadequate glycemic control (HbA1c greater than 7% but less
than 9%) at initiation of therapy, patient currently receiving optimal mealtime insulin
therapy. If taking Symlin in previous 6 months, patient demonstrated a reduction in
HbA1c since initiating Symlin therapy.

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TARCEVA
Affected Drugs
TARCEVA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
For 1st line therapy of locally advanced or metastatic NSCLC, patient should have a
known active EGFR mutation or amplification of the EGFR gene.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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TARGRETIN
Affected Drugs
TARGRETIN®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Pregnancy.
Required Medical Information
For capsules, patient meets one of the following: 1) cutaneous T cell lymphoma
(includes mycosis fungoides [MF] and Sezary syndrome [SS]) refractory to prior
systemic therapy, 2) advanced-stage MF/Sezary syndrome, 3) early-stage MF
refractory/progressive to skin-directed therapy, or 4) early-stage MF with blood
involvement or folliculotropic/large cell transformation.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
Patient has been instructed on the importance of and proper utilization of
contraception.

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TASIGNA
Affected Drugs
TASIGNA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Long QT syndrome, uncorrected electrolyte disorders (hypokalemia,
hypomagnesemia).
Required Medical Information
ECG obtained at baseline, 7-10 days after initiation of therapy and periodically
throughout therapy. Newly diagnosed chronic myeloid leukemia (CML) must be positive
for the Philadelphia chromosome or BCR-ABL gene. For CML [Chronic Myeloid
Leukemia], patient meets one of the following: 1) newly diagnosed in chronic phase, 2)
resistance to imatinib, 3) intolerance/toxicity to imatinib or dasatinib, or 4) relapse after
stem cell transplant.
Age Restrictions
18 years of age and older.
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
Patient has been instructed to avoid eating food 2 hours before and 1 hour after
taking Tasigna. Concomitant use of drugs known to prolong the QT interval and strong
CYP3A4 inhibitors should be avoided.

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TAZORAC
Affected Drugs
TAZORAC®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
For patients being treated for plaque psoriasis Tazorac will be applied to less than
20 percent of the body surface area. For female patients who are able to bear children
(no hysterectomy, not reached menopause, has achieved menses), a negative
pregnancy test (sensitivity down to at least 50 mIU/mL for hCG) must be obtained within
2 weeks prior to Tazorac therapy, beginning during a normal menstrual cycle. Physician
must discuss with the patient the potential risks of fetal harm and importance of birth
control while using Tazorac.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
For patients being treated for plaque psoriasis a trial of at least two topical
corticosteroids (clobetasol, fluocinonide, mometasone, triamcinolone) (patient may still
be using a corticosteroid product in addition to Tazorac) or patient has a
contraindication to topical corticosteroids.
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TESTOSTERONES
Affected Drugs
ANDRODERM®
TESTIM®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Female, prostate cancer, breast cancer.
Required Medical Information
Before the start of testosterone therapy patient has (or patient currently has) a
confirmed low testosterone level (i. e. total testosterone less than 300 ng/dL, free or
bioavailable, testosterone less than 5 ng/dL) or absence of endogenous testosterone.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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THALOMID
Affected Drugs
THALOMID®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Pregnancy.
Required Medical Information
For active myeloma, patient meets one of the following: 1) Thalomid is used as
salvage or palliative therapy. 2) Thalomid is used for newly diagnosed disease or as
primary induction therapy in combination with dexamethasone or in combination with
melphalan and prednisone in nontransplant candidates. 3) Thalomid is used as
maintenance monotherapy following response to either stem cell transplant or primary
induction therapy. For female patients of childbearing potential, pregnancy is excluded
by a negative pregnancy test.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
Patients are monitored for signs and symptoms of thromboembolism. Male and
female patients of child-bearing potential are instructed on the importance of proper
utilization of appropriate contraceptive methods.

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THIORIDAZINE
Affected Drugs
THIORIDAZINE HCL
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Not covered for those who are 65 years of age and older.
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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TOPICAL IMMUNOSUPPRESSANT
Affected Drugs
ELIDEL®
PROTOPIC®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
A. The diagnosis is documented as atopic dermatitis or eczema. B. AND patients
must be at least 2 years of age C. AND patients who have completed a documented
trial and failure of at least two medium or higher potency topical steroids or have
documented intolerance or unresponsiveness to medium or higher potency topical
steroids D. AND patients have been advised that Elidel and Protopic should only be
used to treat the immediate problem and then should be stopped when the condition
improves.
Age Restrictions
2 years of age and older.
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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TOPICAL-ULCERS
Affected Drugs
REGRANEX®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Neoplasm(s) at site(s) of application.
Required Medical Information
A. Must be used for treatment of lower-extremity diabetic ulcers B. AND the ulcer
must extend into subcutaneous tissue or beyond C. AND the tissue must have an
adequate blood supply D. AND the patient must have concurrent good ulcer treatment
practices including ALL of the following: a. Debridement b. Pressure relief c. Infection
relief E. AND the ulcer must be less than 10 cm2 in size.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
10 weeks.
Other Criteria
N/A

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TRACLEER
Affected Drugs
TRACLEER®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
AST/ALT level greater than 3 times upper limit of normal (ULN). Pregnancy.
Concomitant use of cyclosporine A or glyburide.
Required Medical Information
PAH [Pulmonary Arterial Hypertension] confirmed by right heart catheterization.
NYHA Class II-IV symptoms.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
Female patients of childbearing potential must use more than one method of
contraception concurrently.

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TYKERB
Affected Drugs
TYKERB®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
Liver function tests must be monitored at baseline and every four to six weeks during
therapy and as clinically indicated. In patients with severe hepatic impairment, Tykerb is
used at a reduced dose.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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TYZEKA
Affected Drugs
TYZEKA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Use of Tyzeka as a first-line therapy in treatment-nave patients with HBV.
Required Medical Information
A. The patient has been diagnosed with chronic hepatitis B. B. AND the patient has
evidence of a positive HBsAg (+ or -) serological marker for greater than 6 months OR
evidence by a liver biopsy showing chronic hepatitis. C. AND the patient has a Hepatitis
B viral load greater than 20, 000 IU/mL (100, 000 copies per mL) except if for HBeAgnegative HBV, the viral load is greater than 2, 000 IU per mL (10, 000 copies per mL).
D. AND the patient has elevations in liver aminotransferases (ALT or AST) that are two
(2) times greater than normal OR normal liver aminotransferase (ALT or AST) levels
with evidence of significant disease found on biopsy. E. AND the patient has been
tested for HIV and is negative. F. AND if the patient has received previous Tyzeka
treatment, there is documented clinical improvement shown by a drop in viral load or
reduction in the patient's liver aminotransferases. G. AND the patient is not receiving
duplicate therapy that includes Baraclude, Epivir and/or Intron A. H. AND evidence of
diagnosis, serological markers or liver biopsy, viral load, and liver aminotransferases is
documented in patient's chart.
Age Restrictions
16 years of age and older.
Prescriber Restrictions
Infectious Disease specialist or Gastroenterologist or affiliated with an infectious
disease or gastroenterology practice or a primary care physician with experience in
treating HBV.
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Coverage Duration
Plan Year.
Other Criteria
N/A

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VIMPAT
Affected Drugs
VIMPAT®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
A. The patient will receive Vimpat as an adjunctive anticonvulsant for the treatment
of partial onset seizures. B. The patient had a previous or present
trial/failure/contraindication to two or more of the following: carbamazepine, divalproex,
ethosuximide, ethotoin, gabapentin, lamotrigine, levetiracetam, methsuximide,
oxcarbazepine, phenytoin, phenobarbital, pregabalin, rufinamide, tiagabine, topiramate,
valproic acid or zonisamide.
Age Restrictions
17 years of age and older.
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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VOTRIENT
Affected Drugs
VOTRIENT®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Alanine transaminase (ALT) greater than 3 times the upper limit of normal (ULN) and
bilirubin greater than 2 times the ULN.
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
Oncologist.
Coverage Duration
Plan Year.
Other Criteria
N/A

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VPRIV
Affected Drugs
VPRIV®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Concomitant use of miglustat (Zavesca).
Required Medical Information
Diagnosis confirmed by bone marrow histology, DNA testing, or measurement of
beta-glucocerebrosidase enzyme activity of less than 30 percent. Patient must have at
least one of the following conditions as a result of Type 1 Gaucher disease: anemia,
thrombocytopenia, bone disease, hepatomegaly, or splenomegaly. Patients who have
previously received 24 months of VPRIV therapy must have one of the following
responses to continue therapy: 1) A decrease in liver and spleen volume 2) An increase
in platelet count, or 3) An increase in hemoglobin concentration.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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XENAZINE
Affected Drugs
XENAZINE®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Patients with untreated or inadequately treated depression or who are actively
suicidal, history of hepatic disease, use in combination with MAO inhibitors or reserpine
(or it has been less than 20 days since reserpine was discontinued).
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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XIFAXAN
Affected Drugs
XIFAXAN®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Hypersensitivity reaction to rifamycin antimicrobial agents. For hepatic
encephalopathy, Xifaxan exceeding the recommended dose of two 550mg tablets daily.
Required Medical Information
N/A
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
Hepatic encephalopathy-6 months.
Other Criteria
N/A

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XOLAIR
Affected Drugs
XOLAIR®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
N/A
Required Medical Information
N/A
Age Restrictions
12 years of age and older.
Prescriber Restrictions
Pulmonologist, allergist or immunologist.
Coverage Duration
Plan Year.
Other Criteria
To continue therapy, patients must demonstrate an improvement in asthma control
with use of Xolair.

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XYREM
Affected Drugs
XYREM®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
If the patient is taking/receiving any of the following: anxiolytics, sedatives,
hypnotics, barbiturates, benzodiazepines or ethanol.
Required Medical Information
A. The diagnosis is documented as excessive daytime sleepiness with symptoms
that limit their ability to perform normal daily activities. B. AND the diagnosis is
documented as cataplexy (a condition characterized by weak or paralyzed muscles) in
patients with narcolepsy. C. AND if the patient has received prior treatment with Xyrem,
the patient must experience a decrease in daytime sleepiness and/or cataplexy in a
narcoleptic patient.
Age Restrictions
N/A
Prescriber Restrictions
N/A
Coverage Duration
3 months.
Other Criteria
N/A

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ZAVESCA
Affected Drugs
ZAVESCA®
Covered Uses
All FDA approved indications not otherwise excluded from Part D.
Exclusion Criteria
Severe renal impairment. Pregnancy.
Required Medical Information
Diagnosis confirmed by bone marrow histology, DNA testing, or bglucocerebrosidase enzyme assay (enzyme activity less than 30 percent). Trial of
enzyme replacement therapy (ERT) or ERT is not a therapeutic option (eg, allergy, poor
venous access). Female patients of childbearing age will use an effective method of
contraception. Female patients of childbearing age will be educated about the potential
hazards associated with Zavesca use in pregnancy (ie, potential harm to fetus). Must
demonstrate a decrease in liver and spleen volume and/or increase in platelet count
and/or increase in Hgb concentration in patients who received at least 24 months of
Zavesca therapy.
Age Restrictions
18 years of age and older.
Prescriber Restrictions
N/A
Coverage Duration
Plan Year.
Other Criteria
N/A

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INDEX
ACETYLCYSTEINE, 34
ACTEMRA®, 20
ACTIMMUNE®, 21
ADAGEN®, 22
ADCIRCA®, 23
ADRIAMYCIN, 34
AFINITOR®, 24
ALBUTEROL SULFATE, 34
ALDURAZYME®, 25
ALIMTA®, 34
AMIFOSTINE, 34
AMINOSYN II 3.5% M-DEXTROSE
5%®, 34
AMINOSYN II 3.5%-DEXTROSE 25%®,
34
AMINOSYN II 3.5%-DEXTROSE 5%®,
34
AMINOSYN II 4.25%-DEXTROSE
25%®, 34
AMINOSYN II 5% IN 25%
DEXTROSE®, 34
AMINOSYN II IN DEXTROSE®, 34
AMINOSYN II WITH LYTES-CA-DW®,
34
AMINOSYN II®, 34
AMINOSYN M®, 34
AMINOSYN®, 34
AMINOSYN-HBC®, 34
AMINOSYN-HF®, 34
AMINOSYN-PF®, 34
AMIODARONE HCL, 34
AMPHETAMINE SALT COMBO, 27
AMPHOTERICIN B, 34

AMPYRA®, 28
ANADROL-50®, 29
ANAGRELIDE HCL, 30
ANDRODERM®, 128
ANDROXY®, 94
ARALAST NP®, 26
ARCALYST®, 31
ASTRAMORPH-PF®, 34
AVASTIN®, 34
AVONEX ADMINISTRATION PACK®,
33
AVONEX®, 33
AZASAN®, 34
AZATHIOPRINE, 34
AZATHIOPRINE SODIUM, 34
BANZEL®, 39
BICNU®, 34
BLEOMYCIN SULFATE, 34
BUDESONIDE, 34
BUPRENORPHINE HCL, 40
BUSULFEX®, 34
BYETTA®, 41
CALCITRIOL, 34
CAMPATH®, 34
CAMPRAL®, 42
CARBOPLATIN, 34
CARISOPRODOL, 65
CAYSTON®, 43
CELLCEPT®, 35
CEREZYME®, 44
CHANTIX®, 45
CHLORZOXAZONE, 65
CHORIONIC GONADOTROPIN, 60
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CIMZIA®, 46
CISPLATIN, 35
CLADRIBINE, 35
CLINIMIX E®, 35
CLINIMIX®, 35
CLINISOL®, 35
COLISTIMETHATE SODIUM, 35
COPAXONE®, 47
COSMEGEN®, 35
CROMOLYN SODIUM, 35
CUBICIN®, 35
CYCLOBENZAPRINE HCL, 65
CYCLOPHOSPHAMIDE, 35
CYCLOSPORINE, 35
CYCLOSPORINE MODIFIED, 35
CYPROHEPTADINE HCL, 65
CYTARABINE, 35
DACARBAZINE, 35
DAUNORUBICIN HCL, 35
DEPO-PROVERA®, 35
DEXRAZOXANE, 35
DEXTROAMPHETAMINE SULFATE, 27
DICYCLOMINE HCL, 65
DIPHENOXYLATE-ATROPINE, 65
DIPHTHERIA-TETANUS TOXOID®, 35
DIPYRIDAMOLE, 65
DOXIL®, 35
DOXORUBICIN HCL, 35
DRONABINOL, 48
DURAMORPH®, 35
ELAPRASE®, 50
ELIDEL®, 131
ELITEK®, 35
ELSPAR®, 35

EMEND®, 35
EMSAM®, 51
ENGERIX-B®, 35
EPIRUBICIN HCL, 35
EPLERENONE, 52
ESTROPIPATE, 65
ETOPOSIDE, 35
EXJADE®, 54
EXTAVIA®, 55
FABRAZYME®, 56
FASLODEX®, 35
FAZACLO®, 32
FENTANYL, 57
FENTANYL CITRATE, 35, 93
FLUDARABINE PHOSPHATE®, 35
FLUOROURACIL, 35
FORTEO®, 96
FREAMINE III WITH
ELECTROLYTES®, 35
FREAMINE III®, 35
GAMASTAN S-D®, 35
GAMMAGARD LIQUID®, 74
GAMUNEX®, 74
GANCICLOVIR SODIUM, 36
GEMZAR®, 36
GENGRAF, 36
GILENYA®, 58
GLEEVEC®, 59
GRANISETRON HCL, 36
HEPARIN SODIUM, 36
HEPARIN SODIUM IN 0.45% NACL, 36
HEPARIN SODIUM IN 0.9% NACL, 36
HEPARIN SODIUM IN 5% DEXTROSE,
36
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HEPATAMINE®, 36
HEPATASOL®, 36
HEPSERA®, 63
HERCEPTIN®, 36
HUMIRA®, 67
HYDROMORPHONE HCL, 36
HYDROXYZINE HCL, 65
HYDROXYZINE PAMOATE, 65
IDARUBICIN HCL, 36
IFEX®, 36
IFOSFAMIDE, 36
IFOSFAMIDE-MESNA, 36
INCRELEX®, 69
INFERGEN®, 70
INTRALIPID®, 36
INTRON A®, 36
INVEGA SUSTENNA®, 71
IPRATROPIUM BROMIDE, 36
IPRATROPIUM-ALBUTEROL, 36
IRINOTECAN HCL, 36
ISTODAX®, 36
ITRACONAZOLE, 72
KUVAN®, 75
LETAIRIS®, 76
LEUCOVORIN CALCIUM, 36
LEUKINE®, 77
LEUPROLIDE ACETATE, 80
LEVALBUTEROL CONCENTRATE, 36
LEVOCARNITINE, 36
LIDODERM®, 79
LIPOSYN II®, 36
LIPOSYN III, 36
LUPRON DEPOT®, 80
LUPRON DEPOT-PED®, 80

MELPHALAN HCL, 36
MESNA, 36
METADATE ER, 82
METAXALONE, 65
METHOCARBAMOL, 65
METHOTREXATE, 36
METHYLIN, 82
METHYLPHENIDATE HCL, 82
METHYLPHENIDATE SR, 82
MIACALCIN®, 36
MITOMYCIN, 36
MITOXANTRONE HCL, 36
MORPHINE SULFATE, 36
MOZOBIL®, 83
MUSTARGEN®, 36
MYCOPHENOLATE MOFETIL, 37
MYFORTIC®, 37
MYOZYME®, 84
NAGLAZYME®, 85
NEORAL®, 37
NEPHRAMINE®, 37
NEUMEGA®, 37
NEUPOGEN®, 86
NEXAVAR®, 88
NICOTROL NS®, 89
NICOTROL®, 89
NORDITROPIN FLEXPRO®, 61
NORDITROPIN NORDIFLEX®, 61
NOVAREL, 60
NUEDEXTA®, 90
NUVIGIL®, 91
OCTREOTIDE ACETATE, 92
ONDANSETRON HCL, 37
ONDANSETRON ODT, 37
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ONTAK®, 37
ORFADIN®, 95
ORPHENADRINE CITRATE, 65
ORPHENADRINE COMPOUND, 65
ORPHENADRINE COMPOUND
FORTE, 65
ORTHO-EST®, 65
OXALIPLATIN, 37
OXANDROLONE, 29
OXSORALEN-ULTRA®, 97
PACLITAXEL, 37
PEGASYS®, 98
PEGINTRON REDIPEN®, 100
PEGINTRON®, 100
PENTOSTATIN, 37
PERFOROMIST®, 37
PHENADOZ, 65
PHOTOFRIN®, 37
PREGNYL®, 60
PREMASOL®, 37
PROCALAMINE®, 37
PROCRIT®, 53
PROGRAF®, 37
PROLEUKIN®, 37
PROMACTA®, 101
PROMETHAZINE HCL, 65
PROMETHAZINE VC, 65
PROMETHEGAN, 65
PROSOL®, 37
PROTOPIC®, 131
PULMOZYME®, 37
RANEXA®, 103
RAPAMUNE®, 37
REBETOL®, 111

REBIF®, 104
RECOMBIVAX HB®, 37
REGRANEX®, 132
RELISTOR®, 105
REMICADE®, 106
REMODULIN®, 37
REVATIO®, 108
REVLIMID®, 109
RIBAPAK, 111
RIBASPHERE, 111
RIBAVIRIN, 111
RISPERDAL CONSTA®, 113
RITUXAN®, 114
SABRIL®, 115
SANCUSO®, 116
SANDIMMUNE®, 37
SANDOSTATIN LAR®, 117
SOMATULINE DEPOT®, 118
SOMAVERT®, 119
SPRYCEL®, 120
STRATTERA®, 121
SUBOXONE®, 40
SUTENT®, 122
SYMLIN®, 123
SYMLINPEN 120®, 123
SYMLINPEN 60®, 123
TACROLIMUS, 37
TARCEVA®, 124
TARGRETIN®, 125
TASIGNA®, 126
TAXOTERE®, 37
TAZORAC®, 127
TESTIM®, 128

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TETANUS DIPHTHERIA TOXOIDS®,
37
TETANUS TOXOID ADSORBED, 37
TETANUS-DIPHTERIA-DECAVAC®, 37
THALOMID®, 129
THIORIDAZINE HCL, 130
TOBI®, 37
TOPOSAR, 37
TOPOTECAN HCL, 37
TPN ELECTROLYTES®, 37
TRACLEER®, 133
TRANSDERM-SCOP®, 65
TRAVASOL®, 37
TREANDA®, 37
TRELSTAR®, 37
TRIMETHOBENZAMIDE HCL, 65
TRISENOX®, 38
TROPHAMINE®, 38
TYKERB®, 134

TYZEKA®, 135
VANCOMYCIN HCL, 38
VELCADE®, 38
VIDAZA®, 38
VIMPAT®, 137
VINBLASTINE SULFATE, 38
VINCRISTINE SULFATE, 38
VINORELBINE TARTRATE, 38
VOTRIENT®, 138
VPRIV®, 139
XENAZINE®, 140
XIFAXAN®, 141
XOLAIR®, 142
XYREM®, 143
ZAVESCA®, 144
ZEMPLAR®, 38
ZOMETA®, 38
ZORTRESS®, 38

GuildNet Gold HMO-POS SNP and GuildNet Health Advantage HMO-POS SNP are
Coordinated Care plans with a Medicare Advantage contract and a contract with the
New York Medicaid program.
Updated 09/2011

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