Health Canada
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First Nations, Inuit and Aboriginal Health

Drug Benefit List 2010

92:00 UNCLASSIFIED THERAPEUTIC AGENTS

92:00.00 UNCLASSIFIED THERAPEUTIC AGENTS

ABATACEPT

Limited use benefit (prior approval required).

For the treatment of:

  • Rheumatoid Arthritis according to established criteria.
  • Juvenile Idiopathic Arthritis.

(Please refer to Appendix A).

250mg/Vial Injection
2282097 ORENCIA BMS

ADALIMUMAB

Limited use benefit (prior approval required).

For the treatment of:

  1. Rheumatoid Arthritis according to established criteria.
  2. Psoriatic Arthritis according to established criteria.
  3. Ankylosing Spondylitis according to established criteria.
  4. Psoriasis according to established criteria.
  5. Crohn's disease according to established criteria.

(Please refer to Appendix A).

40mg/0.8mL Injection
9857327 HUMIRA PEN ABB
97799757 HUMIRA PEN ABB
9857326 HUMIRA PRE-FILL ABB
97799756 HUMIRA PRE-FILL ABB
40mg/Vial Injection
2258595 HUMIRA ABB

ALENDRONATE SODIUM

Limited use benefit (prior approval required).

For the treatment of:

  1. Osteoporosis in patients who are 65 years of age and over or
  2. Osteoporosis in patients who have documented hip, vertebral or other fractures or
  3. Paget's Disease or
  4. Osteoporosis in patients with no evidence of fracture but who have a high (>20%) 10-year fracture risk or
  5. Osteoporosis in patients with moderate 10-year fracture risk (10-20%) and use of systemic glucocorticoid therapy > 3 months
5mg Tablet
2248727 APO-ALENDRONATE APX
2233055 FOSAMAX FRS
2270110 GEN-ALENDRONATE GEN
2248251 NOVO-ALENDRONATE NOP
2288079 SANDOZ ALENDRONATE SDZ
10mg Tablet
2248728 APO-ALENDRONATE APX
2201011 FOSAMAX FRS
2270129 GEN-ALENDRONATE GEN
2247373 NOVO-ALENDRONATE NOP
2288087 SANDOZ ALENDRONATE SDZ

ALENDRONATE SODIUM

Limited use benefit (prior approval required).

For the treatment of:

  1. Osteoporosis in patients who are 65 years of age and over or
  2. Osteoporosis in patients who have documented hip, vertebral or other fractures or
  3. Paget's Disease or
  4. Osteoporosis in patients with no evidence of fracture but who have a high (>20%) 10-year fracture risk or
  5. Osteoporosis in patients with moderate 10-year fracture risk (10-20%) and use of systemic glucocorticoid therapy > 3 months
40mg Tablet
2258102 CO ALENDRONATE COB
2201038 FOSAMAX FRS
70mg Tablet
2303078 ALENDRONATE-70 PDL
2248730 APO-ALENDRONATE APX
2258110 CO ALENDRONATE COB
2245329 FOSAMAX FRS
2286335 GEN-ALENDRONATE GEN
2261715 NOVO-ALENDRONATE NOP
2299712 PHL-ALENDRONATE PMI
2273179 PMS-ALENDRONATE PMS
2284006 PMS-ALENDRONATE FC PMS
2275279 RATIO-ALENDRONATE RPH
2270889 RIVA-ALENDRONATE RIV
2288109 SANDOZ ALENDRONATE SDZ
2302004 ZYM-ALENDRONATE ZYM

ALENDRONATE SODIUM, VITAMIN D3

Limited use benefit (prior approval required).

For the treatment of:

  1. Osteoporosis in patients who are 65 years of age and over or
  2. Osteoporosis in patients who have documented hip, vertebral or other fractures or
  3. Paget's Disease or
  4. Osteoporosis in patients with no evidence of fracture but who have a high (>20%) 10-year fracture risk or
  5. Osteoporosis in patients with moderate 10-year fracture risk (10-20%) and use of systemic glucocorticoid therapy > 3 months
70mg/2800U Tablet
2276429 FOSAVANCE FRS
70mg/5600U Tablet
2314940 FOSAVANCE MSP

ALFUZOSIN HYDROCHLORIDE

10mg Sustained Release Tablet
2315866 APO-ALFUZOSIN ER APX
2304678 SANDOZ ALFUZOSIN SDZ
2245565 XATRAL SAC

ALLOPURINOL

100mg Tablet
449687 ALLOPRIN VAE
555681 ALLOPURINOL PDL
402818 APO-ALLOPURINOL APX
364282 NOVO-PUROL NOP
200mg Tablet
514209 ALLOPRIN VAE
2130157 ALLOPURINOL PDL
479799 APO-ALLOPURINOL APX
565342 NOVO-PUROL NOP
300mg Tablet
454354 ALLOPRIN VAE
555703 ALLOPURINOL PDL
402796 APO-ALLOPURINOL APX
363693 NOVO-PUROL NOP
294322 ZYLOPRIM GSK

AZATHIOPRINE

50mg Tablet
2242907 APO-AZATHIOPRINE APX
4596 IMURAN GSK
2248843 NU-AZATHIOPRINE NXP

BETAHISTINE HCL

16mg Tablet
2280191 NOVO-BETAHISTINE NOP
2243878 SERC SPH
24mg Tablet
2280205 NOVO-BETAHISTINE NOP
2247998 SERC SPH

BOTULINUM TOXIN TYPE A

Limited use benefit (prior approval required).

For the treatment of:

  1. strabismus and blepharospasm associated with dystonia, including benign essential blepharospasm or VII nerve disorder in patients 12 years of age or older
  2. cervical dystonia (spasmodic torticollis)
100IU Injection
1981501 BOTOX ALL

CABERGOLINE

Limited use benefit (prior approval required).

For treatment of hyperprolactinemia in patients who have failed therapy with or are intolerant to bromocriptine.

0.5mg Tablet
2301407 CO CABERGOLINE COB
2242471 DOSTINEX PFI

CLOSTRIDIUM BOTULINUM NEUROTOXIN

Limited use benefit (prior approval required).

For:

  1. the treatment of strabismus and blepharospasm associated with dystonia, including benign essential blepharospasm or VII nerve disorder in patients 12 years of age or older or
  2. the treatment of cervical dystonia (spasmodic torticollis)
100U/vial Injection
2324032 XEOMIN MEZ

COLCHICINE

0.6mg Tablet
572349 COLCHICINE ODN
1mg Tablet
621374 COLCHICINE ODN

CYCLOSPORINE

Limited use benefit (prior approval required).

For transplant therapy.

10mg Capsule
2237671 NEORAL NVR
25mg Capsule
2150689 NEORAL NVR
2247073 SANDOZ-CYCLOSPORINE SDZ
50mg Capsule
2150662 NEORAL NVR
2247074 SANDOZ-CYCLOSPORINE SDZ
100mg Capsule
2150670 NEORAL NVR
2242821 SANDOZ-CYCLOSPORINE SDZ
100mg/mL Solution
2150697 NEORAL NVR

CYPROTERONE ACETATE, ETHINYL ESTRADIOL

2mg & 35mcg Tablet
2290308 CYESTRA-35 PMS
2233542 DIANE-35 BAY
2309556 NOVO-CYPROTERONE/ETHINYL ESTRADIOL NOP

DUTASTERIDE

Limited use benefit (prior approval required).

  1. For treatment of Benign Prostatic Hyperplasia (BPH) in patients who do not tolerate or have not responded to an adrenergic blocker.
    or
  2. For use in combination therapy when monotherapy with an alpha-blocker is not sufficient.
0.5mg Capsule
2247813 AVODART GSK

ERGOCALCIFEROL

8288IU/mL Oral Liquid
80003615 ERDOL ODN

ETANERCEPT

Limited use benefit (prior approval required).

For the treatment of:

  • Rheumatoid Arthritis according to established criteria.
  • Psoriatic Arthritis according to established criteria.
  • Ankylosing Spondylitis according to established criteria.
  • Juvenile Idiopathic Arthritis

(Please refer to Appendix A).

25mg/Vial Injection
2242903 ENBREL IMX
50mg/mL Injection
2274728 ENBREL IMX
99100373 ENBREL SURECLICK AMG

ETIDRONATE DISODIUM

200mg Tablet
2248686 CO ETIDRONATE COB
1997629 DIDRONEL PGP
2245330 GEN-ETIDRONATE GEN

ETIDRONATE DISODIUM, CALCIUM CARBONATE

400mg & 500mg Tablet
2263866 CO-ETIDROCAL COB
2176017 DIDROCAL PGP
2247323 GEN-ETI-CAL CP GEN
2324199 NOVO-ETIDRONATECAL KIT NOP

EXTEMPORANEOUS MIXTURE

Miscellaneous
990019 EXTEMPORANEOUS MIXTURE *
999994 EXTEMPORANEOUS MIXTURE *
999997 EXTEMPORANEOUS MIXTURE *
999999 EXTEMPORANEOUS MIXTURE *
915000 STERILE EXTEMPORANEOUS MIXTURE (QC)

FINASTERIDE

Limited use benefit (prior approval required).

  1. For treatment of Benign Prostatic Hyperplasia (BPH) in patients who do not tolerate or have not responded to an alpha-adrenergic blocker.
    or
  2. For use in combination therapy when monotherapy with an alpha-blocker is not sufficient.
5mg Tablet
2348500 NOVO-FINASTERIDE NOP
2310112 PMS-FINASTERIDE PMS
2010909 PROSCAR FRS
2306905 RATIO-FINASTERIDE RPH
2322579 SANDOZ FINASTERIDE SDZ

FLUNARIZINE HCL

5mg Capsule
2246082 APO-FLUNARIZINE APX

GOLIMUMAB

Limited use benefit (prior approval required).

For the treatment of:

  • Rheumatoid Arthritis according to established criteria.
  • Psoriatic Arthritis according to established criteria.
  • Ankylosing Spondylitis according to established criteria.

(Please refer to Appendix A).

50mg/0.5mL Injection
2324784 SIMPONI AUTO INJECTOR CER
2324776 SIMPONI PRE-FILLED SYRINGE CER

INFLIXIMAB

Limited use benefit (prior approval required).

For treatment of:

  • Fistulizing Crohn’s disease according to established criteria.
  • For adult patients with moderately to severely active Crohn’s Disease who have had an inadequate response to conventional therapy.
    (Please refer to Appendix A).
    or
  • Rheumatoid Arthritis according to established criteria

(Please refer to Appendix A).

100mg/Vial Injection
2244016 REMICADE CEN

LANREOTIDE

60mg/0.3mL Injection
2283395 SOMATULINE AUTOGEL IPS
90mg/0.3mL Injection
2283409 SOMATULINE AUTOGEL IPS
120mg/0.5mL Injection
2283417 SOMATULINE AUTOGEL IPS

LEFLUNOMIDE

Limited use benefit (prior approval required).

For treatment of patients with rheumatoid arthritis who:

  1. have failed treatment with methotrexate: weekly dose (PO, SC or IM) of 20mg or greater (15mg or greater if patient is 65 years of age or older) for more than 8 weeks.
  2. cannot tolerate or have contraindications to methotrexate.
10mg Tablet
2256495 APO-LEFLUNOMIDE APX
2241888 ARAVA SAC
2319225 GEN-LEFLUNOMIDE GEN
2261251 NOVO-LEFLUNOMIDE NOP
2288265 PMS-LEFLUNOMIDE PMS
2283964 SANDOZ LEFLUNOMIDE SDZ
20mg Tablet
2256509 APO-LEFLUNOMIDE APX
2241889 ARAVA SAC
2319233 GEN-LEFLUNOMIDE GEN
2261278 NOVO-LEFLUNOMIDE NOP
2288273 PMS-LEFLUNOMIDE PMS
2283972 SANDOZ LEFLUNOMIDE SDZ

LEUCOVORIN CALCIUM

5mg Tablet
2170493 LEUCOVORIN CALCIUM WAY

MYCOPHENOLATE MOFETIL

Limited use benefit (prior approval required).

For transplant therapy.

250mg Capsule
2192748 CELLCEPT HLR
500mg Tablet
2237484 CELLCEPT HLR

MYCOPHENOLATE SODIUM

Limited use benefit (prior approval required).

For transplant therapy.

180mg Enteric Coated Tablet
2264560 MYFORTIC NVR
360mg Enteric Coated Tablet
2264579 MYFORTIC NVR

NEDOCROMIL SODIUM

2% Ophth Solution
2241407 ALOCRIL ALL

OCTREOTIDE

10mg/Vial Injection
2239323 SANDOSTATIN LAR NVR
20mg/Vial Injection
2239324 SANDOSTATIN LAR NVR
30mg/Vial Injection
2239325 SANDOSTATIN LAR NVR
50mcg/mL Injection
2248639 OCTREOTIDE ACETATE OMEGA OMG
839191 SANDOSTATIN NVR
100mcg/mL Injection
2248640 OCTREOTIDE ACETATE OMEGA OMG
839205 SANDOSTATIN NVR
200mcg/mL Injection
2248642 OCTREOTIDE ACETATE OMEGA OMG
2049392 SANDOSTATIN NOV
500mcg/mL Injection
2248641 OCTREOTIDE ACETATE OMEGA OMG
839213 SANDOSTATIN NVR

PAMIDRONATE DISODIUM

30mg Injection
2059762 AREDIA IV NVR
2244550 PAMIDRONATE DISODIUM MAY
2264951 RHOXAL-PAMIDRONATE RHO
60mg Injection
2244551 PAMIDRONATE DISODIUM HOS
2264978 RHOXAL-PAMIDRONATE SDZ

PAMIDRONATE DISODIUM

90mg Injection
2059789 AREDIA IV NVR
2244552 PAMIDRONATE DISODIUM MAY
2245999 PMS-PAMIDRONATE PMS
2264986 RHOXAL-PAMIDRONATE SDZ

PENTOSAN POLYSULFATE SODIUM

100mg Capsule
2029448 ELMIRON JNO

RISEDRONATE SODIUM

Limited use benefit (prior approval required).

For the treatment of:

  1. Osteoporosis in patients who are 65 years of age and over or
  2. Osteoporosis in patients who have documented hip, vertebral or other fractures or
  3. Paget's Disease or
  4. Osteoporosis in patients with no evidence of fracture but who have a high (>20%) 10-year fracture risk or
  5. Osteoporosis in patients with moderate 10-year fracture risk (10-20%) and use of systemic glucocorticoid therapy > 3 months
5mg Tablet
2242518 ACTONEL PGP
2298376 NOVO-RISEDRONATE NOP
30mg Tablet
2239146 ACTONEL PGP
2298384 NOVO-RISEDRONATE NOP
35mg Tablet
2246896 ACTONEL PGP
2298392 NOVO-RISEDRONATE NOP

SIROLIMUS

Limited use benefit (prior approval required).

Coverage will be provided as a second line therapy for patients failing mycophenolate mofetil.

1mg/mL Oral Liquid
2243237 RAPAMUNE WAY
1mg Tablet
2247111 RAPAMUNE WAY

TAMSULOSIN HCL

0.4mg Long Acting Capsule
2281392 NOVO-TAMSULOSIN NOP
2294885 RAN-TAMSULOSIN RBY
2294265 RATIO-TAMSULOSIN RPH
2295121 SANDOZ TAMSULOSIN SDZ
0.4mg Long Acting Tablet
2270102 FLOMAX CR BOE

TAMSULOSIN HYDROCHLORIDE

0.4mg Sustained Release Capsule
2298570 GEN-TAMSULOSIN MYL

TETRABENAZINE

25mg Tablet
2199270 NITOMAN LHL

USTEKINUMAB

Limited use benefit (prior approval required).

For the treatment of moderate to severe psoriasis in patients who meet the following criteria:

  1. Body surface area involvement greater than 10% and/or significant involvement of the face, hands, feet or genital region and
  2. Intolerance or lack of response to methotrexate and cyclosporine or
  3. A contraindication to methotrexate and/or cyclosporine and
  4. Intolerance or lack of response to phototherapy or
  5. Inability to access phototherapy

Coverage beyond 16 weeks will be based on a significant reduction in the Body Surface Area (BSA) involved and improvements in the Psoriasis Area Severity Index (PASI) score and the Dermatology Life Quality Index (DLQI).

45mg/0.5mL Injection
2320673 STELARA JNO

WATER

100% Injection
38202 STERILE WATER * ABB
99002264 STERILE WATER *
905178 WATER FOR INJECTION *
905194 WATER FOR INJECTION *
905224 WATER FOR INJECTION *

ZOLEDRONIC ACID

Limited use benefit (prior approval required).

For the treatment of Paget’s disease. Coverage will be granted for one dose per 12 month period.

5mg/100mL Injection
2269198 ACLASTA NOV

92:44.00

TACROLIMUS

Limited use benefit (prior approval required).

For transplant therapy.

0.5mg Capsule
2243144 PROGRAF AST
1mg Capsule
2175991 PROGRAF AST
5mg Capsule
2175983 PROGRAF AST
5mg/mL Injection
2176009 PROGRAF AST
0.5mg Long Acting Capsule
2296462 ADVAGRAF AST
1mg Long Acting Capsule
2296470 ADVAGRAF AST
5mg Long Acting Capsule
2296489 ADVAGRAF AST