Drug Benefit List 2010
12:00 AUTONOMIC DRUGS
12:04.00 PARASYMPATHOMIMETIC AGENTS
BETHANECHOL CHLORIDE
- 10mg Tablet
- 1947958 DUVOID SHI
- 1985671 MYOTONACHOL GLE
- 25mg Tablet
- 1947931 DUVOID SHI
- 1985558 MYOTONACHOL GLE
- 50mg Tablet
- 1947923 DUVOID SHI
DONEPEZIL HCL
Limited use benefit (prior approval required).
Initial six month coverage for cholinesterase inhibitors:
- Diagnosis of mild to moderate Alzheimer’s disease; AND
- Mini Mental State Exam (MMSE) score of 10-26, established
within the last 60 days; AND
- Global Deterioration Scale (GDS) score between 4 to 6,
established within the last 60 days
- Continued coverage beyond 6 months will be based on
improvement or stabilization of cognition, function or
behaviour.
Criteria for coverage at every six month interval:
- Diagnosis is still mild to moderate Alzheimer’s disease;
AND
- MMSE score > 10; AND
- GDS score between 4 to 6; AND
- Improvement or stabilization in at least one of the following
domains
(please indicate improved, worsened, or no change)
- Memory, reasoning and perception (e.g., names, tasks,
MMSE)
- Instrumental activities of daily living (IADLs: e.g.,
telephone, shopping, meal preparation)
- Basic activities of daily living (e.g., bathing, dressing,
hygiene, toileting)
- Neuropsychiatric symptoms (e.g., agitation, delusions,
hallucination, apathy)
- 5mg Tablet
- 2232043 ARICEPT PFI
- 10mg Tablet
- 2232044 ARICEPT PFI
GALANTAMINE
Limited use benefit (prior approval required).
Initial six month coverage for cholinesterase inhibitors:
- Diagnosis of mild to moderate Alzheimer’s disease; AND
- Mini Mental State Exam (MMSE) score of 10-26, established
within the last 60 days; AND
- Global Deterioration Scale (GDS) score between 4 to 6,
established within the last 60 days
- Continued coverage beyond 6 months will be based on
improvement or stabilization of cognition, function or
behaviour.
Criteria for coverage at every six month interval:
- Diagnosis is still mild to moderate Alzheimer’s disease;
AND
- MMSE score > 10; AND
- GDS score between 4 to 6; AND
- Improvement or stabilization in at least one of the following
domains
(please indicate improved, worsened, or no change)
- Memory, reasoning and perception (e.g., names, tasks,
MMSE)
- Instrumental activities of daily living (IADLs: e.g.,
telephone, shopping, meal preparation)
- Basic activities of daily living (e.g., bathing, dressing,
hygiene, toileting)
- Neuropsychiatric symptoms (e.g., agitation, delusions,
hallucination, apathy)
- 8mg Extended Release Capsule
- 2266717 REMINYL ER JNO
- 16mg Extended Release Capsule
- 2266725 REMINYL ER JNO
- 24mg Extended Release Capsule
- 2266733 REMINYL ER JNO
NEOSTIGMINE BROMIDE
- 15mg Tablet
- 869945 PROSTIGMIN VAE
PYRIDOSTIGMINE BROMIDE
- 180mg Sustained Release Tablet
- 869953 MESTINON-SR VAE
- 60mg Tablet
- 869961 MESTINON VAE
RIVASTIGMINE
Limited use benefit (prior approval required).
Initial six month coverage for cholinesterase inhibitors:
- Diagnosis of mild to moderate Alzheimer’s disease; AND
- Mini Mental State Exam (MMSE) score of 10-26, established
within the last 60 days; AND
- Global Deterioration Scale (GDS) score between 4 to 6,
established within the last 60 days
- Continued coverage beyond 6 months will be based on
improvement or stabilization of cognition, function or
behaviour.
Criteria for coverage at every six month interval:
- Diagnosis is still mild to moderate Alzheimer’s disease;
AND
- MMSE score > 10; AND
- GDS score between 4 to 6; AND
- Improvement or stabilization in at least one of the following
domains (please indicate improved, worsened, or no change)
- Memory, reasoning and perception (e.g., names, tasks,
MMSE)
- Instrumental activities of daily living (IADLs: e.g.,
telephone, shopping, meal preparation)
- Basic activities of daily living (e.g., bathing, dressing,
hygiene, toileting)
- Neuropsychiatric symptoms (e.g., agitation, delusions,
hallucination, apathy)
- 1.5mg Capsule
- 2242115 EXELON NOV
- 2332809 MYLAN-RIVASTIGMINE MYL
- 2305984 NOVO-RIVASTIGMINE NOP
- 2306034 PMS-RIVASTIGMINE PMS
- 2311283 RATIO-RIVASTIGMINE RPH
- 2324563 SANDOZ RIVASTIGMINE SDZ
- 3mg Capsule
- 2242116 EXELON NOV
- 2332817 MYLAN-RIVASTIGMINE MYL
- 2305992 NOVO-RIVASTIGMINE NOP
- 2306042 PMS-RIVASTIGMINE PMS
- 2311291 RATIO-RIVASTIGMINE RPH
- 2324571 SANDOZ RIVASTIGMINE SDZ
- 4.5mg Capsule
- 2242117 EXELON NOV
- 2332825 MYLAN-RIVASTIGMINE MYL
- 2306018 NOVO-RIVASTIGMINE NOP
- 2306050 PMS-RIVASTIGMINE PMS
- 2311305 RATIO-RIVASTIGMINE RPH
- 2324598 SANDOZ RIVASTIGMINE SDZ
- 6mg Capsule
- 2242118 EXELON NOV
- 2332833 MYLAN-RIVASTIGMINE MYL
- 2306026 NOVO-RIVASTIGMINE NOP
- 2306069 PMS-RIVASTIGMINE PMS
- 2311313 RATIO-RIVASTIGMINE RPH
- 2324601 SANDOZ RIVASTIGMINE SDZ
- 2mg/mL Oral Liquid
- 2245240 EXELON NOV
12:08.08 ANTIMUSCARINICS / ANTISPASMODICS
IPRATROPIUM BROMIDE
- 250mcg/mL Inhalation Solution (Multi-Dose)
- 2126222 APO-IPRAVENT APX
- 2239131 GEN-IPRATROPIUM GEN
- 2210479 NOVO-IPRAMIDE NOP
- 2231136 PMS-IPRATROPIUM PMS
- 125mcg/mL Inhalation Solution (Unit Dose)
- 2231135 PMS-IPRATROPIUM UDV PMS
- 2097176 RATIO-IPRATROPIUM UDV RPH
- 250mcg/mL Inhalation Solution (Unit Dose)
- 2216221 GEN-IPRATROPIUM UDV GEN
- 2231785 NU-IPRATROPIUM UDV NXP
- 2231244 PMS-IPRATROPIUM UDV PMS
- 2231245 PMS-IPRATROPIUM UDV PMS
- 2097168 RATIO-IPRATROPIUM UDV RPH
- 99001446 RATIO-IPRATROPIUM UDV * RPH
- 20mcg/Inhalation Inhaler
- 2247686 ATROVENT HFA BOE
- 0.03% Nasal Spray
- 2246083 APO-IPRAVENT APX
- 2240508 DOM-IPRATROPIUM DPC
- 2239627 PMS-IPRATROPIUM PMS
- 0.06% Nasal Spray
- 2246084 APO-IPRAVENT APX
IPRATROPIUM BROMIDE, SALBUTAMOL
- 0.2mg & 1mg/mL Inhalation Solution (Unit Dose)
- 2231675 COMBIVENT BOE
- 2272695 GEN-COMBO GEN
- 2243789 RATIO-IPRA SAL RPH
SCOPOLAMINE BUTYLBROMIDE
- 10mg Tablet
- 363812 BUSCOPAN BOE
TIOTROPIUM BROMIDE MONOHYDRATE
Limited use benefit (prior approval required).
For the treatment of moderate* to severe* chronic obstructive
pulmonary disease (COPD), in patients who continue to be
symptomatic after an adequate trial (3 months) of ipatropium,
at a dose of 8-12 puffs daily.
*Canadian Thoracic Society COPD Classification by
Symptoms/Disability and Lung Function
Moderate: shortness of breath from COPD causing the
patient to stop after walking about 100 meters (after a few
minutes) on level ground (MRC 3 to 4); 50% ≤ FEV1 < 80%
predicted, FEV1/FVC <0.7
Severe: shortness of breath from COPD leaving the patient
too breathless to leave the house or breathless after
undressing (MRC 5), or in the presence of chronic respiratory
failure or clinical signs of right heart failure; 30% ≤ FEV1 <
50% predicted, FEV1/FVC <0.7
- 18mcg Powder for Inhalation (Capsule)
- 2246793 SPIRIVA BOE
12:12.04 ALPHA ADRENERGIC AGONISTS
MIDODRINE HCL
- 2.5mg Tablet
- 1934392 AMATINE SHI
- 5mg Tablet
- 1934406 AMATINE SHI
12:12.08 BETA ADRENERGIC AGONISTS
FORMOTEROL FUMARATE
Limited use benefit (prior approval required).
For the treatment of asthma in patients who are using optimal corticosteroid therapy and experiencing breakthrough symptoms requiring regular use of a rapid onset, short duration bronchodilator. Oxeze is not intended for the relief of acute asthma symptoms: patients must have access to an inhaled fast-acting bronchodilator (beta-2 agonist) for symptomatic relief.
- 12mcg/Capsule Powder for Inhalation
- 2230898 FORADIL NVR
FORMOTEROL FUMARATE DIHYDRATE
- 6mcg/Dose Dry Powder Inhaler
- 2237225 OXEZE TURBUHALER AZC
- 12mcg/Dose Dry Powder Inhaler
- 2237224 OXEZE TURBUHALER AZC
FORMOTEROL FUMARATE DIHYDRATE, BUDESONIDE
Limited use benefit (prior approval required).
For the treatment of reversible obstructive airway disease in patients who are not adequately controlled on medium doses of inhaled corticosteroids ( e.g. fluticasone 250 - 500 mcg daily, or the equivalent) as the sole agent and require addition of a long- acting beta agonist. Patients using this combination product must also have access to a short-acting bronchodilator for symptomatic relief.
- 6mcg & 100mcg/Inhalation Inhaler
- 2245385 SYMBICORT 100 TURBUHALER AZC
- 6mcg & 200mcg/Inhalation Inhaler
- 2245386 SYMBICORT 200 TURBUHALER AZC
ORCIPRENALINE SULFATE
- 2mg/mL Syrup
- 2236783 APO-ORCIPRENALINE APX
- 2192675 TANTA-ORCIPRENALINE TAN
SALBUTAMOL
- 5mg/mL Inhalation Solution (Multi-Dose)
- 2139324 DOM-SALBUTAMOL DPC
- 2232987 GEN-SALBUTAMOL GEN
- 2069571 PMS-SALBUTAMOL PMS
- 860808 RATIO-SALBUTAMOL RPH
- 2154412 SANDOZ-SALBUTAMOL SDZ
- 2213486 VENTOLIN GSK
- 0.5mg/mL Inhalation Solution (Unit Dose)
- 2208245 PMS-SALBUTAMOL PMS
- 2239365 RATIO-SALBUTAMOL RPH
SALBUTAMOL
- 1mg/mL Inhalation Solution (Unit Dose)
- 2216949 DOM-SALBUTAMOL DPC
- 1926934 GEN-SALBUTAMOL GEN
- 2084333 MED-SALBUTAMOL MEC
- 2231783 NU-SALBUTAMOL NXP
- 2208229 PMS-SALBUTAMOL PMS
- 1986864 RATIO-SALBUTAMOL RPH
- 2213419 VENTOLIN PF GSK
- 2mg/mL Inhalation Solution (Unit Dose)
- 2173360 GEN-SALBUTAMOL PF GEN
- 2231784 NU-SALBUTAMOL NXP
- 2208237 PMS-SALBUTAMOL PMS
- 2239366 RATIO-SALBUTAMOL RPH
- 2213427 VENTOLIN PF GSK
- 100mcg/Inhalation Inhaler
- 2232570 AIROMIR MMH
- 2245669 APO-SALVENT CFC FREE APX
- 2326450 NOVO-SALBUTAMOL HFA NOP
- 2244914 RATIO-SALBUTAMOL HFA RPH
- 2241497 VENTOLIN HFA GSK
- 0.4mg/mL Oral Liquid
- 2212390 VENTOLIN GSK
- 400mcg Powder for Inhalation (Capsule)
- 895415 VENTOLIN ROTACAPS * GSK
- 200mcg Powder for Inhalation (Disk)
- 99000369 VENTODISK & DISKHALER * GSK
- 400mcg Powder for Inhalation (Disk)
- 99000377 VENTODISK * GSK
- 2mg Tablet
- 2146843 APO-SALVENT APX
- 4mg Tablet
- 2146851 APO-SALVENT APX
- 2165376 NU-SALBUTAMOL NXP
SALMETEROL XINAFOATE
Limited use benefit (prior approval required).
- For the treatment of asthma in patients who are using optimal corticosteroid therapy and experiencing breakthrough symptoms requiring regular use of a rapid onset, short duration bronchodilator. Serevent is not intended for the relief of acute asthma symptoms: patients must have access to an inhaled fast-acting bronchodilator (beta-2 agonist) for symptomatic relief.
- For the treatment of Chronic Obstructive Pulmonary Disease (COPD) in patients not adequately controlled with ipratropium.
- 50mcg/inhalation Powder Diskus
- 2231129 SEREVENT DISKUS GSK
- 50mcg/Inhalation Powder for Inhalation
- 2214261 SEREVENT DISKHALER GSK
SALMETEROL XINAFOATE, FLUTICASONE PROPIONATE
Limited use benefit (prior approval required).
For treatment of reversible obstructive airway disease in
patients who are not adequately controlled on medium doses
of inhaled corticosteroids (e.g., fluticasone 250-500mcg
daily, or the equivalent) as a sole agent and require addition
of a long-acting beta agonist. Patients using this
combination product must also have access to a short-
acting bronchodilator for symptomatic relief.
For the treatment of moderate* to severe* chronic obstructive
pulmonary disease (COPD), in patients who continue to be
symptomatic after an adequate trial (2-4 months) of
ipatropium, at a dose of 12 puffs daily.
*Canadian Thoracic Society COPD Classification by
Symptoms/Disability
Moderate: shortness of breath from COPD causing the
patient to stop after walking about 100 meters (after a few
minutes) on the level.
Severe: shortness of breath from COPD leaving the patient
too breathless to leave the house or breathless after
undressing, or in the presence of chronic respiratory failure
or clinical signs of right heart failure.
By Symptom/Disability:
Moderate: shortness of breath from COPD causing the
patient to stop after walking approximately 100 meters (or
after a few minutes) on the level.
Severe: shortness of breath from COPD resulting in the
patient being too breathless to leave the house or breathless
after undressing, or the presence of chronic respiratory
failure or clinical signs of right heart failure.
- 25mcg & 125mcg Inhaler
- 2245126 ADVAIR GSK
- 25mcg & 250mcg Inhaler
- 2245127 ADVAIR GSK
- 50mcg & 100mcg Inhaler
- 2240835 ADVAIR DISKUS 100 GSK
- 50mcg & 250mcg Inhaler
- 2240836 ADVAIR DISKUS 250 GSK
- 50mcg & 500mcg Inhaler
- 2240837 ADVAIR DISKUS 500 GSK
TERBUTALINE SULFATE
- 500mcg/Inhalation Powder for Inhalation
- 786616 BRICANYL TURBUHALER AZC
12:12.12 ALPHA AND BETA ADRENERGIC AGONISTS
EPINEPHRINE
- 0.15mg/0.15mL Injection
- 2268205 TWINJECT PAL
- 0.5mg/mL Injection
- 578657 EPIPEN JR AXL
- 1mg/mL Injection
- 155357 ADRENALIN ERF
- 721891 EPINEPHRINE ABB
- 509558 EPIPEN AXL
- 2247310 TWINJECT PAL
EPINEPHRINE
- 1mg/mL Topical Solution
- 155365 ADRENALIN ERF
PSEUDOEPHEDRINE HCL, TRIPROLIDINE HCL
- 60mg & 2.5mg Tablet
- 2238302 ACTIFED PFI
12:16.00 SYMPATHOLYTIC AGENTS
DIHYDROERGOTAMINE MESYLATE
- 1mg/mL Injection
- 27243 DIHYDROERGOTAMINE STE
- 2241163 DIHYDROERGOTAMINE SDZ
- 4mg/mL Nasal Spray
- 2228947 MIGRANAL STE
ERGOTAMINE TARTRATE, CAFFEINE
- 1mg & 100mg Tablet
- 176095 CAFERGOT NVR
METHYSERGIDE MALEATE
- 2mg Tablet
- 27499 SANSERT NVR
12:20.24 CENTRALL ACTING SKELETAL MUSCLE RELAXANTS
CYCLOBENZAPRINE HCL
Limited use benefit (prior approval is not required).
For relief of muscle spasm associated with acute, painful musculoskeletal conditions. Coverage is limited to 60mg per day for three (3) weeks, renewable every two (2) months.
- 10mg Tablet
- 2177145 APO-CYCLOBENZAPRINE APX
- 2220644 CYCLOBENZAPRINE PDL
- 2238633 DOM-CYCLOBENZAPRINE DPC
- 2231353 GEN-CYCLOPRINE GEN
- 2080052 NOVO-CYCLOPRINE NOP
- 2171848 NU-CYCLOBENZAPRINE NXP
- 2249359 PHL-CYCLOBENZAPRINE PHH
- 2212048 PMS-CYCLOBENZAPRINE PMS
- 2236506 RATIO-CYCLOBENZAPRINE RPH
- 2242079 RIVA-CYCLOBENZAPRINE RIV
TIZANIDINE HCL
Limited use benefit (prior approval required).
For treatment of spasticity in patients with multiple sclerosis, who have failed therapy with or are intolerant to baclofen.
- 4mg Tablet
- 2259893 APO-TIZANIDINE APX
- 2272059 GEN-TIZANIDINE GEN
- 2239170 ZANAFLEX ELN
12:20.08 DIRECT-ACTING SKELETAL MUSCLE RELAXANTS
DANTROLENE SODIUM
- 25mg Capsule
- 1997602 DANTRIUM PGP
- 100mg Capsule
- 1997653 DANTRIUM PGP
12:20.12 GABA-DERIVATIVE SKELETAL MUSCLE RELAXANTS
BACLOFEN
- 10mg Tablet
- 2139332 APO-BACLOFEN APX
- 2152584 BACLOFEN PDL
- 2138271 DOM-BACLOFEN DPC
- 2088398 GEN-BACLOFEN GEN
- 455881 LIORESAL NVR
- 2084449 MED-BACLOFEN MEC
- 2136090 NU-BACLO NXP
- 2236963 PHL-BACLOFEN PHH
- 2063735 PMS-BACLOFEN PMS
- 2236507 RATIO-BACLOFEN RPH
- 2242150 RIVA-BACLOFEN RIV
- 20mg Tablet
- 2139391 APO-BACLOFEN APX
- 2152592 BACLOFEN PDL
- 2138298 DOM-BACLOFEN DPC
- 2088401 GEN-BACLOFEN GEN
- 636576 LIORESAL DS NVR
- 2084457 MED-BACLOFEN MEC
- 2136104 NU-BACLO NXP
- 2236964 PHL-BACLOFEN PHH
- 2063743 PMS-BACLOFEN PMS
- 2236508 RATIO-BACLOFEN RPH
- 2242151 RIVA-BACLOFEN RIV
12:92.00 MISCELLANEOUS AUTONOMIC DRUGS
NICOTINE (GUM)
Limited use benefit with quantity and frequency limits (prior approval is not required).
For smoking cessation:
Coverage is limited to 945 pieces during a one-year period. The year starts on the date the first prescription is filled. Once this quantity has been reached, the client is eligible again for coverage for nicotine gum when one year has elapsed from the day the initial prescription was filled.
- 2mg Gum
- 2091933 NICORETTE JNO
- 4mg Gum
- 2091941 NICORETTE PLUS PMJ
NICOTINE (PATCH)
Limited use benefit with quantity and frequency limits (prior approval is not required).
For smoking cessation:
Coverage will be provided for up to the allowable number of patches for one of the following products, during a one-year period. The year starts on the date the first prescription is filled. The number of patches covered in the one-year period is:
- Habitrol 84 patches or
- Nicoderm 70 patches or
- Nicotrol 70 patches
Once this quantity has been reached, the client is eligible again for coverage for nicotine patches when one year has elapsed from the day the initial prescription was filled.
- 7mg Patch (Habitrol)
- 1943057 HABITROL NVC
- 14mg Patch (Habitrol)
- 1943065 HABITROL NVC
- 21mg Patch (Habitrol)
- 1943073 HABITROL NVC
- 36mg Patch (Nicoderm)
- 2093111 NICODERM PMJ
- 78mg Patch (Nicoderm)
- 2093138 NICODERM PMJ
- 114mg Patch (Nicoderm)
- 2093146 NICODERM PMJ
- 8.3mg/10cm2 Patch (Nicotrol)
- 2065738 NICOTROL TRANSDERMAL JNO
- 16.6mg/20cm2 Patch (Nicotrol)
- 2065754 NICOTROL TRANSDERMAL JNO
- 24.9mg/30cm2 Patch (Nicotrol)
- 2065762 NICOTROL TRANSDERMAL JNO
VARENICLINE
Limited use benefit with quantity and frequency limits (prior approval is not required).
Coverage will be limited to 165 tablets during a one-year period. The year starts on the date the first prescription is filled. Once this quantity has been reached, the client is eligible again for coverage for varenicline (Champix®) when one year has elapsed from the day the initial prescription was filled.
- 0.5mg Tablet
- 2291177 CHAMPIX PFI
- 0.5mg & 1mg Tablet
- 2298309 CHAMPIX STARTER PACK PFI
- 1mg Tablet
- 2291185 CHAMPIX PFI