Results 1 - 198 of 198
| Brand name | Kivexa | |
|---|---|---|
| Manufacturer | GlaxoSmithKline | |
| Indication | HIV infection | |
| Submission type | Initial | |
| Date submission received | 2005-07-26 | |
| Status | Complete | |
| Date recommendation issued | 2005-12-07 | Recommendation and reasons |
| Recommendation | List in a similar manner to other drugs in class |
| Brand name | Orencia | |
|---|---|---|
| Manufacturer | Bristol-Myers Squibb Canada | |
| Indication | Arthritis, Rheumatoid | |
| Submission type | Resubmission #1 | |
| Date submission received | 2009-12-02 | |
| Status | Complete | |
| Date recommendation issued | 2010-06-17 | Recommendation and reasons |
| Recommendation | List in a similar manner |
| Brand name | Orencia | |
|---|---|---|
| Manufacturer | Bristol-Myers Squibb Canada | |
| Indication | Arthritis, Juvenile Idiopathic & Juvenile Rheumatoid | |
| Submission type | New Indication | |
| Date submission received | 2008-08-29 | |
| Status | Complete | |
| Date recommendation issued | 2009-04-22 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Orencia | |
|---|---|---|
| Manufacturer | Bristol-Myers Squibb Canada | |
| Indication | Arthritis, Rheumatoid | |
| Submission type | Initial | |
| Date submission received | 2006-10-26 | |
| Status | Complete | |
| Date recommendation issued | 2007-06-27 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Campral | |
|---|---|---|
| Manufacturer | Prempharm Inc. | |
| Indication | Alcohol Abstinence | |
| Submission type | Request for Advice | |
| Date submission received | 2008-07-22 | |
| Status | Complete |
| Brand name | Campral | |
|---|---|---|
| Manufacturer | Prempharm Inc. | |
| Indication | Alcohol Abstinence | |
| Submission type | Initial | |
| Date submission received | 2007-08-29 | |
| Status | Complete | |
| Date recommendation issued | 2008-03-27 | Recommendation and reasons |
| Recommendation | List with criteria/condition | |
| Plain language recommendation | Plain language recommendation | |
| Summary of CEDAC Discussion | Summary of CEDAC Discussion | |
| Overview of CDR reports | Overview of CDR reports | |
| Brand name | Humira | |
|---|---|---|
| Manufacturer | Abbott Laboratories, Limited | |
| Indication | Psoriasis | |
| Submission type | New Indication | |
| Date submission received | 2008-04-15 | |
| Status | Complete | |
| Date recommendation issued | 2008-10-16 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Humira | |
|---|---|---|
| Manufacturer | Abbott Laboratories, Limited | |
| Indication | Crohn's disease | |
| Submission type | Resubmission #3 | |
| Date submission received | 2007-07-12 | |
| Status | Complete | |
| Date recommendation issued | 2007-12-19 | Recommendation and reasons |
| Recommendation | List with criteria/condition | |
| Plain language recommendation | Plain language recommendation | |
| Summary of CEDAC Discussion | Summary of CEDAC Discussion | |
| Overview of CDR reports | Overview of CDR reports | |
| Brand name | Humira | |
|---|---|---|
| Manufacturer | Abbott Laboratories, Limited | |
| Indication | Ankylosing spondylitis (AS) | |
| Submission type | Resubmission #2 | |
| Date submission received | 2006-11-17 | |
| Status | Complete | |
| Date recommendation issued | 2007-06-27 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Humira | |
|---|---|---|
| Manufacturer | Abbott Laboratories Limited | |
| Indication | Arthritis, psoriatic | |
| Submission type | Resubmission #1 | |
| Date submission received | 2006-06-21 | |
| Status | Complete | |
| Date recommendation issued | 2006-11-29 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Humira | |
|---|---|---|
| Manufacturer | Abbott Laboratories Limited | |
| Indication | Arthritis, rheumatoid | |
| Submission type | Initial | |
| Date submission received | 2004-09-24 | |
| Status | Complete | |
| Date recommendation issued | 2005-02-11 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Hepsera | |
|---|---|---|
| Manufacturer | gilead Sciences Canada Inc. | |
| Indication | Hepatitis B | |
| Submission type | Request for Advice | |
| Date submission received | 2007-06-29 | |
| Status | Complete | |
| Date recommendation issued | 2007-10-18 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Hepsera | |
|---|---|---|
| Manufacturer | Gilead Sciences Canada Inc. | |
| Indication | Hepatitis B | |
| Submission type | Initial | |
| Date submission received | 2006-04-24 | |
| Status | Complete | |
| Date recommendation issued | 2006-11-29 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Replagal | |
|---|---|---|
| Manufacturer | Transkaryotic Therapies Inc. | |
| Indication | Fabry Disease | |
| Submission type | Initial | |
| Date submission received | 2004-02-19 | |
| Status | Complete | |
| Date recommendation issued | 2004-11-24 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Fabrazyme | |
|---|---|---|
| Manufacturer | Genzyme Canada | |
| Indication | Fabry Disease | |
| Submission type | Resubmission #1 | |
| Date submission received | 2004-12-10 | |
| Status | Complete | |
| Date recommendation issued | 2005-05-18 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Fabrazyme | |
|---|---|---|
| Manufacturer | Genzyme Canada | |
| Indication | Fabry Disease | |
| Submission type | Initial | |
| Date submission received | 2004-02-24 | |
| Status | Complete | |
| Date recommendation issued | 2004-11-24 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Amevive | |
|---|---|---|
| Manufacturer | Biogen Idec Canada Inc. | |
| Indication | Psoriasis, moderate to severe chronic plaque | |
| Submission type | Resubmission #1 | |
| Date submission received | 2006-02-28 | |
| Status | Complete | |
| Date recommendation issued | 2006-09-27 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Amevive | |
|---|---|---|
| Manufacturer | Biogen Idec Canada Inc. | |
| Indication | Psoriasis, moderate to severe chronic plaque | |
| Submission type | Initial | |
| Date submission received | 2004-11-16 | |
| Status | Complete | |
| Date recommendation issued | 2005-05-26 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Fosavance 70/5600 | |
|---|---|---|
| Manufacturer | Merck Frosst Canda Ltd. | |
| Indication | Osteoporosis | |
| Submission type | Initial | |
| Date submission received | 2008-12-18 | |
| Status | Complete | |
| Date recommendation issued | 2009-06-17 | Recommendation and reasons |
| Recommendation | List in a similar manner to other drugs in class |
| Brand name | Fosavance | |
|---|---|---|
| Manufacturer | Merck Frosst Canda Ltd. | |
| Indication | Osteoporosis | |
| Submission type | Initial | |
| Date submission received | 2006-03-27 | |
| Status | Complete | |
| Date recommendation issued | 2006-09-27 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Myozyme | |
|---|---|---|
| Manufacturer | Genzyme Canada Inc. | |
| Indication | Pompe’s disease | |
| Submission type | Initial | |
| Date submission received | 2006-10-10 | |
| Status | Complete | |
| Date recommendation issued | 2007-06-14 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Rasilez | |
|---|---|---|
| Manufacturer | Novartis Pharmaceuticals Canada Inc. | |
| Indication | Hypertension | |
| Submission type | Initial | |
| Date submission received | 2007-11-30 | |
| Status | Complete | |
| Date recommendation issued | 2008-06-25 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Axert | |
|---|---|---|
| Manufacturer | Janssen-Ortho Inc. | |
| Indication | Migraine | |
| Submission type | Initial | |
| Date submission received | 2003-12-24 | |
| Status | Complete | |
| Date recommendation issued | 2004-05-27 | Recommendation and reasons |
| Recommendation | List in a similar manner to other drugs in class |
| Brand name | Volibris | |
|---|---|---|
| Manufacturer | GlaxoSmithKline Inc. | |
| Indication | Pulmonary arterial hypertension (WHO class II and III) | |
| Submission type | Initial | |
| Date submission received | 2008-07-09 | |
| Status | Complete | |
| Date recommendation issued | 2008-12-17 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Caduet | |
|---|---|---|
| Manufacturer | Pfizer Canada Inc. | |
| Indication | Hypertension/ Dyslipidemia | |
| Submission type | Initial | |
| Date submission received | 2005-12-15 | |
| Status | Complete | |
| Date recommendation issued | 2006-05-17 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Emend | |
|---|---|---|
| Manufacturer | Merck Frosst Canada Ltd. | |
| Indication | Chemotherapy induced Nausea and Vomiting | |
| Submission type | Initial | |
| Date submission received | 2007-08-29 | |
| Status | Complete | |
| Date recommendation issued | 2008-02-20 | Recommendation and reasons |
| Recommendation | List with criteria/condition | |
| Plain language recommendation | Plain language recommendation | |
| Summary of CEDAC Discussion | Summary of CEDAC Discussion | |
| Overview of CDR reports | Overview of CDR reports | |
| Brand name | Abilify | |
|---|---|---|
| Manufacturer | Bristol-Myers Squibb Canada | |
| Indication | Schizophrenia | |
| Submission type | Initial | |
| Date submission received | 2009-11-06 | |
| Status | Complete | |
| Date recommendation issued | 2010-04-27 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Reyataz | |
|---|---|---|
| Manufacturer | Bristol Myers Squibb | |
| Indication | HIV infection | |
| Submission type | Initial | |
| Date submission received | 2003-12-16 | |
| Status | Complete | |
| Date recommendation issued | 2004-05-27 | Recommendation and reasons |
| Recommendation | List in a similar manner to other drugs in class |
| Brand name | Strattera | |
|---|---|---|
| Manufacturer | Eli Lilly Canada Inc. | |
| Indication | Attention deficit hyperactivity disorder | |
| Submission type | Request for Advice | |
| Date submission received | 2006-09-25 | |
| Status | Complete |
| Brand name | Strattera | |
|---|---|---|
| Manufacturer | Eli Lilly Canada Inc. | |
| Indication | Attention deficit hyperactivity disorder | |
| Submission type | Initial | |
| Date submission received | 2005-01-25 | |
| Status | Complete | |
| Date recommendation issued | 2005-09-28 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Finacea | |
|---|---|---|
| Manufacturer | Bayer Inc. | |
| Indication | Rosacea | |
| Submission type | Initial | |
| Project Number | TBA | |
| Date submission received | 2010-08-31 | |
| Patient input deadline | 2010-09-22 | Patient Input |
| Status | Active | |
| Brand name | Combigan Ophthalmic Solution | |
|---|---|---|
| Manufacturer | Allergan Canada Inc. | |
| Indication | Glaucoma | |
| Submission type | Initial | |
| Date submission received | 2003-12-15 | |
| Status | Complete | |
| Date recommendation issued | 2004-05-27 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Azarga | |
|---|---|---|
| Manufacturer | Alcon Canada Inc. | |
| Indication | Glaucoma and Ocular hypertension | |
| Submission type | Initial | |
| Date submission received | 2009-08-28 | |
| Status | Complete | |
| Date recommendation issued | 2010-02-18 | Recommendation and reasons |
| Recommendation | List in a similar manner to other drugs in class |
| Brand name | Suboxone | |
|---|---|---|
| Manufacturer | Schering-Plough Canada Inc | |
| Indication | Opioid drug dependence (Substitution treatment) | |
| Submission type | Initial | |
| Date submission received | 2008-03-06 | |
| Status | Complete | |
| Date recommendation issued | 2008-09-24 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Gynazole.1 | |
|---|---|---|
| Manufacturer | Ferring Pharmaceuticals | |
| Indication | Vaginal infection | |
| Submission type | Initial | |
| Date submission received | 2004-06-30 | |
| Status | Complete | |
| Date recommendation issued | 2005-01-26 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Silkis | |
|---|---|---|
| Manufacturer | Galderma Canada Inc. | |
| Indication | Psoriasis, mild to moderate plaque | |
| Submission type | Initial | |
| Date submission received | 2010-03-15 | |
| Status | Active |
| Brand name | Ilaris | |
|---|---|---|
| Manufacturer | Novartis Pharmaceuticals Canada Inc. | |
| Indication | Cryopyrin-Associated Periodic Syndrome (CAPS) | |
| Submission type | Initial | |
| Project Number | S0204 | |
| Date submission received | 2010-07-07 | |
| Patient input deadline | 2010-07-28 | |
| Status | Active | |
| Brand name | Stalevo | |
|---|---|---|
| Manufacturer | Novartis Pharmaceuticals Canada Inc. | |
| Indication | Parkinsons Disease | |
| Submission type | Initial | |
| Date submission received | 2008-04-15 | |
| Status | Complete | |
| Date recommendation issued | 2008-10-16 | Recommendation and reasons |
| Recommendation | List in a similar manner |
| Brand name | Cimzia | |
|---|---|---|
| Manufacturer | UCB Pharma Canada Inc. | |
| Indication | Arthritis, rheumatoid | |
| Submission type | Initial | |
| Date submission received | 2009-09-03 | |
| Status | Complete | |
| Date recommendation issued | 2010-05-27 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Alvesco | |
|---|---|---|
| Manufacturer | Altana Pharma Inc. | |
| Indication | asthma | |
| Submission type | Initial | |
| Date submission received | 2006-07-24 | |
| Status | Complete | |
| Date recommendation issued | 2006-12-20 | Recommendation and reasons |
| Recommendation | List |
| Brand name | Omnaris | |
|---|---|---|
| Manufacturer | Nycomed Canada Inc. | |
| Indication | Allergic Rhinitis (seasonal and perennial) | |
| Submission type | Initial | |
| Date submission received | 2008-05-07 | |
| Status | Complete | |
| Date recommendation issued | 2008-11-12 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Sensipar | |
|---|---|---|
| Manufacturer | Amgen Canada Inc. | |
| Indication | Secondary hyper-parathyroidism in chronic kidney disease | |
| Submission type | Initial | |
| Date submission received | 2004-08-20 | |
| Status | Complete | |
| Date recommendation issued | 2005-03-23 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Ciprodex | |
|---|---|---|
| Manufacturer | Alcon Canada Inc. | |
| Indication | Otitis media with otorrhea & otitis externa, acute | |
| Submission type | Request for Advice | |
| Date submission received | 2007-06-15 | |
| Status | Complete | |
| Date recommendation issued | 2007-10-18 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Ciprodex | |
|---|---|---|
| Manufacturer | Alcon Canada Inc. | |
| Indication | Otitis media with otorrhea & otitis externa, acute | |
| Submission type | Initial | |
| Date submission received | 2004-06-11 | |
| Status | Complete | |
| Date recommendation issued | 2005-01-26 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Xeomin | |
|---|---|---|
| Manufacturer | Merz Pharmaceuticals GmbH | |
| Indication | Post-stroke Spasticity | |
| Submission type | Initial | |
| Date submission received | 2009-06-12 | |
| Status | Complete | |
| Date recommendation issued | 2009-12-16 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Xeomin | |
|---|---|---|
| Manufacturer | Merz Pharmaceuticals GmbH | |
| Indication | Blepharospasm | |
| Submission type | Initial | |
| Date submission received | 2009-06-12 | |
| Status | Complete | |
| Date recommendation issued | 2009-12-16 | Recommendation and reasons |
| Recommendation | List in a similar manner |
| Brand name | Xeomin | |
|---|---|---|
| Manufacturer | Merz Pharmaceuticals GmbH | |
| Indication | Cervical Dystonia | |
| Submission type | Initial | |
| Date submission received | 2009-06-12 | |
| Status | Complete | |
| Date recommendation issued | 2009-12-16 | Recommendation and reasons |
| Recommendation | List in a similar manner |
| Brand name | Pradax | |
|---|---|---|
| Manufacturer | Boehringer-Ingelheim (Canada) Ltd. | |
| Indication | Prevention of stroke, systemic embolism and reduction of vascular mortality in patients with atrial fibrillation | |
| Submission type | Pre-NOC - New Indication | |
| Project Number | S0202 | |
| Date submission received | 2010-05-31 | |
| Patient input deadline | 2010-06-25 | |
| Status | Complete | |
| Brand name | Pradax | |
|---|---|---|
| Manufacturer | Boehringer Ingelheim (Canada) Ltd. | |
| Indication | Venous thromboembolism prevention | |
| Submission type | Initial | |
| Date submission received | 2008-07-08 | |
| Status | Complete | |
| Date recommendation issued | 2009-01-28 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Cubicin | |
|---|---|---|
| Manufacturer | Cubist Pharmaceuticals Inc. | |
| Indication | Skin and Skin Structure Infections & Bacteremia | |
| Submission type | Initial | |
| Date submission received | 2008-03-06 | |
| Status | Complete | |
| Date recommendation issued | 2008-09-24 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Enablex | |
|---|---|---|
| Manufacturer | Novartis Pharmaceuticals Canada Inc. | |
| Indication | Bladder, overactive | |
| Submission type | Resubmission #1 | |
| Date submission received | 2008-10-01 | |
| Status | Complete | |
| Date recommendation issued | 2009-04-16 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Enablex | |
|---|---|---|
| Manufacturer | Novartis Pharmaceuticals Canada Inc. | |
| Indication | Bladder, overactive | |
| Submission type | Initial | |
| Date submission received | 2006-04-26 | |
| Status | Complete | |
| Date recommendation issued | 2006-10-19 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Prezista | |
|---|---|---|
| Manufacturer | Janssen-Ortho Inc. | |
| Indication | HIV infection (Pediatric) | |
| Submission type | New Indication | |
| Date submission received | 2009-12-22 | |
| Status | Complete | |
| Date recommendation issued | 2010-06-17 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Prezista | |
|---|---|---|
| Manufacturer | Janssen-Ortho Inc. | |
| Indication | HIV - treatment naive | |
| Submission type | New Indication | |
| Date submission received | 2009-03-27 | |
| Status | Complete | |
| Date recommendation issued | 2009-10-14 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Prezista | |
|---|---|---|
| Manufacturer | Janssen-Ortho Inc. | |
| Indication | HIV infection | |
| Submission type | Initial | |
| Date submission received | 2006-08-29 | |
| Status | Complete | |
| Date recommendation issued | 2007-02-14 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Exjade | |
|---|---|---|
| Manufacturer | Novartis Pharmaceuticals Canada Inc. | |
| Indication | Iron overload | |
| Submission type | Initial | |
| Date submission received | 2006-10-26 | |
| Status | Complete | |
| Date recommendation issued | 2007-04-19 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Sativex | |
|---|---|---|
| Manufacturer | GW Pharma Ltd. | |
| Indication | Cancer Pain (adjunctive analgesia to maximum tolerated strong opioids) | |
| Submission type | Resubmission #1 | |
| Date submission received | 2007-08-07 | |
| Status | Complete | |
| Date recommendation issued | 2008-02-20 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Sativex | |
|---|---|---|
| Manufacturer | GW Pharma Ltd. | |
| Indication | Neuropathic pain (adjunctive) in MS. | |
| Submission type | Initial | |
| Date submission received | 2007-02-27 | |
| Status | Complete | |
| Date recommendation issued | 2007-09-26 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Prolia | |
|---|---|---|
| Manufacturer | Amgen Canada Inc. | |
| Indication | Postmenopausal osteoporosis | |
| Submission type | Initial | |
| Project Number | S0208 | |
| Date submission received | 2010-08-26 | |
| Patient input deadline | 2010-09-17 | Patient Input |
| Status | Active | |
| Brand name | Pristiq | |
|---|---|---|
| Manufacturer | Wyeth Canada | |
| Indication | Major Depressive Disorder (MDD) | |
| Submission type | Initial | |
| Date submission received | 2009-03-05 | |
| Status | Complete | |
| Date recommendation issued | 2009-09-23 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Multaq | |
|---|---|---|
| Manufacturer | Sanofi-Aventis Canada Inc. | |
| Indication | Atrial fibrillation | |
| Submission type | Initial | |
| Date submission received | 2009-09-18 | |
| Status | Complete | |
| Date recommendation issued | 2010-05-27 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Yasmin | |
|---|---|---|
| Manufacturer | Berlex Canada Inc. | |
| Indication | Contraceptive, oral | |
| Submission type | Initial | |
| Date submission received | 2005-01-20 | |
| Status | Complete | |
| Date recommendation issued | 2005-06-16 | Recommendation and reasons |
| Recommendation | List |
| Brand name | Cymbalta | |
|---|---|---|
| Manufacturer | Eli Lilly Canada Inc. | |
| Indication | Neuropathic pain, Diabetic | |
| Submission type | Initial | |
| Date submission received | 2008-02-08 | |
| Status | Complete | |
| Date recommendation issued | 2008-08-14 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Cymbalta | |
|---|---|---|
| Manufacturer | Eli Lilly Canada Inc. | |
| Indication | Major Depressive Disorder (MDD) | |
| Submission type | Initial | |
| Date submission received | 2008-02-08 | |
| Status | Complete | |
| Date recommendation issued | 2008-08-14 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Avodart | |
|---|---|---|
| Manufacturer | GlaxoSmithKline Inc. | |
| Indication | Prostatic hyperplasia, benign | |
| Submission type | Initial | |
| Date submission received | 2004-08-24 | |
| Status | Complete | |
| Date recommendation issued | 2005-01-20 | Recommendation and reasons |
| Recommendation | List in a similar manner to other drugs in class |
| Brand name | Soliris | |
|---|---|---|
| Manufacturer | Alexion Pharmaceuticals Inc. | |
| Indication | Paroxysmal nocturnal hemoglobinuria (PNH) | |
| Submission type | Initial | |
| Date submission received | 2009-09-18 | |
| Status | Complete | |
| Date recommendation issued | 2010-02-18 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Raptiva | |
|---|---|---|
| Manufacturer | Serono Canada Inc. | |
| Indication | Psoriasis, moderate to severe chronic plaque | |
| Submission type | Request for Advice | |
| Date submission received | 2007-06-19 | |
| Status | Complete |
| Brand name | Raptiva | |
|---|---|---|
| Manufacturer | Serono Canada Inc. | |
| Indication | Psoriasis, moderate to severe chronic plaque | |
| Submission type | Initial | |
| Date submission received | 2005-10-25 | |
| Status | Complete | |
| Date recommendation issued | 2006-08-24 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Atripla | |
|---|---|---|
| Manufacturer | Bristol-Myers Squibb and Gilead Sciences | |
| Indication | HIV | |
| Submission type | Initial | |
| Date submission received | 2007-10-30 | |
| Status | Complete | |
| Date recommendation issued | 2008-04-17 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Relpax | |
|---|---|---|
| Manufacturer | Pfizer Canada Inc. | |
| Indication | Migraine | |
| Submission type | Initial | |
| Date submission received | 2004-09-21 | |
| Status | Complete | |
| Date recommendation issued | 2005-03-23 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Truvada | |
|---|---|---|
| Manufacturer | Gilead Sciences Canada Inc. | |
| Indication | HIV infection | |
| Submission type | Request for Advice | |
| Date submission received | 2008-07-07 | |
| Status | Complete | |
| Date recommendation issued | 2008-12-17 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Updated recommendation issued | 2008-12-17 | Recommendation and reasons |
|---|---|---|
| Brand name | Truvada | |
| Manufacturer | Gilead Sciences Canada Inc. | |
| Indication | HIV infection | |
| Submission type | Initial | |
| Date submission received | 2006-05-29 | |
| Status | Complete | |
| Date recommendation issued | 2006-10-25 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Baraclude | |
|---|---|---|
| Manufacturer | Bristol-Myers Squibb Canada | |
| Indication | Hepatitis B (chronic) | |
| Submission type | Initial | |
| Date submission received | 2006-12-12 | |
| Status | Complete | |
| Date recommendation issued | 2007-11-28 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Inspra | |
|---|---|---|
| Manufacturer | Pfizer Canada Inc. | |
| Indication | Post myocardial infarction | |
| Submission type | Initial | |
| Date submission received | 2009-05-06 | |
| Status | Complete | |
| Date recommendation issued | 2009-11-25 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Teveten Plus | |
|---|---|---|
| Manufacturer | Solvay Pharma Inc. | |
| Indication | High blood pressure | |
| Submission type | Initial | |
| Date submission received | 2004-07-08 | |
| Status | Complete | |
| Date recommendation issued | 2004-12-15 | Recommendation and reasons |
| Recommendation | List in a similar manner to other drugs in class |
| Brand name | Tarceva | |
|---|---|---|
| Manufacturer | Hoffmann-La Roche Limited | |
| Indication | Lung cancer, non-small cell | |
| Submission type | Initial | |
| Date submission received | 2005-07-19 | |
| Status | Complete | |
| Date recommendation issued | 2005-12-07 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Cipralex | |
|---|---|---|
| Manufacturer | Lundbeck Canada Inc. | |
| Indication | Depression, Major Depressive Disorder (MDD) | |
| Submission type | Resubmission #1 | |
| Date submission received | 2006-06-08 | |
| Status | Complete | |
| Date recommendation issued | 2007-01-24 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Cipralex | |
|---|---|---|
| Manufacturer | Lundbeck Canada Inc. | |
| Indication | Depression, Major Depressive Disorder (MDD) | |
| Submission type | Initial | |
| Date submission received | 2005-08-03 | |
| Status | Withdrawn |
| Brand name | NuvaRing | |
|---|---|---|
| Manufacturer | Organon Canada Ltd. | |
| Indication | Contraceptive, ring | |
| Submission type | Initial | |
| Date submission received | 2006-05-05 | |
| Status | Complete | |
| Date recommendation issued | 2006-11-29 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Intelence | |
|---|---|---|
| Manufacturer | Janssen-Ortho Inc. | |
| Indication | HIV | |
| Submission type | Initial | |
| Date submission received | 2008-04-02 | |
| Status | Complete | |
| Date recommendation issued | 2008-08-14 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Telzir | |
|---|---|---|
| Manufacturer | GlaxoSmithKline Inc. | |
| Indication | HIV infection | |
| Submission type | Initial | |
| Date submission received | 2005-01-24 | |
| Status | Complete | |
| Date recommendation issued | 2005-06-16 | Recommendation and reasons |
| Recommendation | List in a similar manner to other drugs in class |
| Brand name | Iressa | |
|---|---|---|
| Manufacturer | AstraZeneca | |
| Indication | Lung cancer, non-small cell | |
| Submission type | Initial | |
| Date submission received | 2003-12-22 | |
| Status | Complete | |
| Date recommendation issued | 2004-06-23 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Copaxone | |
|---|---|---|
| Manufacturer | Teva Pharmaceutical Industries Ltd. | |
| Indication | Clinically Isolated Syndrome (CIS), suggestive of Multiple Sclerosis | |
| Submission type | New Indication | |
| Date submission received | 2009-04-29 | |
| Status | Complete | |
| Date recommendation issued | 2009-11-25 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Simponi | |
|---|---|---|
| Manufacturer | Centocor Inc. | |
| Indication | Arthritis, rheumatoid | |
| Submission type | Initial | |
| Date submission received | 2009-09-03 | |
| Status | Complete | |
| Date recommendation issued | 2010-03-17 | Recommendation and reasons |
| Recommendation | List in a similar manner |
| Brand name | Simponi | |
|---|---|---|
| Manufacturer | Centocor Inc. | |
| Indication | Ankylosing spondylitis | |
| Submission type | Initial | |
| Date submission received | 2009-09-03 | |
| Status | Complete | |
| Date recommendation issued | 2010-03-17 | Recommendation and reasons |
| Recommendation | List in a similar manner |
| Brand name | Simponi | |
|---|---|---|
| Manufacturer | Centocor Inc. | |
| Indication | Arthritis, psoriatic | |
| Submission type | Initial | |
| Date submission received | 2009-09-03 | |
| Status | Complete | |
| Date recommendation issued | 2010-03-17 | Recommendation and reasons |
| Recommendation | List in a similar manner |
| Brand name | Vantas | |
|---|---|---|
| Manufacturer | Paladin Labs Inc. | |
| Indication | Prostate Cancer | |
| Submission type | Initial | |
| Date submission received | 2006-09-20 | |
| Status | Complete | |
| Date recommendation issued | 2007-04-26 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Jurnista | |
|---|---|---|
| Manufacturer | Janssen-Ortho Inc. | |
| Indication | Chronic Pain (moderate to severe) | |
| Submission type | Initial | |
| Date submission received | 2009-12-04 | |
| Status | Complete | |
| Date recommendation issued | 2010-05-19 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Elaprase | |
|---|---|---|
| Manufacturer | Shire Human Genetic Therapies, Inc. | |
| Indication | Mucopolysarccharidosis II (MPS II), Hunter Syndrome | |
| Submission type | Initial | |
| Date submission received | 2007-07-13 | |
| Status | Complete | |
| Date recommendation issued | 2007-12-19 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Remicade | |
|---|---|---|
| Manufacturer | Centocor Inc. | |
| Indication | Ulcerative Colitis | |
| Submission type | Initial | |
| Date submission received | 2008-09-29 | |
| Status | Complete | |
| Date recommendation issued | 2009-04-22 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | NovoMix 30 | |
|---|---|---|
| Manufacturer | Novo Nordisk Canada Inc. | |
| Indication | Diabetes mellitus | |
| Submission type | Initial | |
| Date submission received | 2005-10-13 | |
| Status | Complete | |
| Date recommendation issued | 2006-04-26 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Levemir | |
|---|---|---|
| Manufacturer | Novo Nordisk Canada Inc. | |
| Indication | Diabetes Mellitus Type1, Pediatrics | |
| Submission type | New Indication | |
| Date submission received | 2009-03-10 | |
| Status | Complete | |
| Date recommendation issued | 2009-08-19 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Levemir | |
|---|---|---|
| Manufacturer | Novo Nordisk Canada Inc. | |
| Indication | Diabetes mellitus | |
| Submission type | Resubmission #2 | |
| Date submission received | 2009-03-10 | |
| Status | Complete | |
| Date recommendation issued | 2009-08-19 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Levemir | |
|---|---|---|
| Manufacturer | Novo Nordisk Canada Inc. | |
| Indication | Diabetes mellitus | |
| Submission type | Resubmission #1 | |
| Date submission received | 2009-02-02 | |
| Status | Withdrawn |
| Brand name | Levemir | |
|---|---|---|
| Manufacturer | Novo Nordisk Canada Inc. | |
| Indication | Diabetes mellitus | |
| Submission type | Initial | |
| Date submission received | 2005-12-19 | |
| Status | Complete | |
| Date recommendation issued | 2006-08-02 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Lantus | |
|---|---|---|
| Manufacturer | Sanofi-Aventis Canada Inc. | |
| Indication | Diabetes, Type 1 & 2 | |
| Submission type | Request for Advice | |
| Date submission received | 2009-06-09 | |
| Status | Complete |
| Brand name | Lantus | |
|---|---|---|
| Manufacturer | Sanofi-Aventis Canada Inc. | |
| Indication | Diabetes, Type 1 & 2 | |
| Submission type | Resubmission #1 | |
| Date submission received | 2006-03-27 | |
| Status | Complete | |
| Date recommendation issued | 2006-10-25 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Lantus | |
|---|---|---|
| Manufacturer | Aventis Pharma Inc. | |
| Indication | Diabetes, Type 1 & 2 | |
| Submission type | Initial | |
| Date submission received | 2005-02-11 | |
| Status | Complete | |
| Date recommendation issued | 2005-09-28 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Apidra | |
|---|---|---|
| Manufacturer | Sanofi-Aventis Canada Inc. | |
| Indication | Diabetes (Type 1 & 2) | |
| Submission type | Initial | |
| Date submission received | 2008-08-29 | |
| Status | Complete | |
| Date recommendation issued | 2009-02-19 | Recommendation and reasons |
| Recommendation | List in a similar manner to other drugs in class |
| Brand name | Somatuline Autogel | |
|---|---|---|
| Manufacturer | Ipsen Limited | |
| Indication | Acromegaly | |
| Submission type | Initial | |
| Date submission received | 2007-02-20 | |
| Status | Complete | |
| Date recommendation issued | 2007-07-19 | Recommendation and reasons |
| Recommendation | List in a similar manner to other drugs in class |
| Brand name | Fosrenol | |
|---|---|---|
| Manufacturer | Shire BioChem Inc. | |
| Indication | Hyperphosphatemia, end-stage renal disease | |
| Submission type | Initial | |
| Date submission received | 2007-06-28 | |
| Status | Complete | |
| Date recommendation issued | 2008-01-30 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Aldurazyme | |
|---|---|---|
| Manufacturer | Genzyme Canada | |
| Indication | Mucopolysarccharidosis 1 (MPS 1), Hurler, Hurler-Scheie, Scheie | |
| Submission type | Initial | |
| Date submission received | 2005-02-03 | |
| Status | Complete | |
| Date recommendation issued | 2005-07-14 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Duodopa | |
|---|---|---|
| Manufacturer | Solvay Pharma Inc. | |
| Indication | Parkinson's disease | |
| Submission type | Initial | |
| Date submission received | 2008-12-19 | |
| Status | Complete | |
| Date recommendation issued | 2009-07-22 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Vyvanse | |
|---|---|---|
| Manufacturer | Shire Canada Inc. | |
| Indication | Attention deficit hyperactivity disorder | |
| Submission type | Initial | |
| Date submission received | 2009-07-10 | |
| Status | Complete | |
| Date recommendation issued | 2009-12-18 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Lotemax | |
|---|---|---|
| Manufacturer | Bausch & Lomb | |
| Indication | Post-operative inflammation following cataract surgery | |
| Submission type | Initial | |
| Date submission received | 2009-12-02 | |
| Status | Complete | |
| Date recommendation issued | 2010-05-19 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Prexige | |
|---|---|---|
| Manufacturer | Novartis Pharmaceuticals Canada Inc. | |
| Indication | Osteoarthritis (Knee) | |
| Submission type | Initial | |
| Date submission received | 2006-12-15 | |
| Status | Complete | |
| Date recommendation issued | 2007-07-25 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Celsentri | |
|---|---|---|
| Manufacturer | Pfizer Canada Inc. | |
| Indication | HIV | |
| Submission type | Resubmission #1 | |
| Date submission received | 2008-05-07 | |
| Status | Complete | |
| Date recommendation issued | 2008-11-12 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Celsentri | |
|---|---|---|
| Manufacturer | Pfizer Canada Inc. | |
| Indication | HIV | |
| Submission type | Initial | |
| Date submission received | 2007-11-02 | |
| Status | Withdrawn |
| Brand name | Ebixa | |
|---|---|---|
| Manufacturer | Lundbeck Canada Inc. | |
| Indication | Dementia of the Alzheimer type, moderate to severe | |
| Submission type | Initial | |
| Date submission received | 2004-12-21 | |
| Status | Complete | |
| Date recommendation issued | 2005-11-23 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Relistor | |
|---|---|---|
| Manufacturer | Wyeth Canada | |
| Indication | Constipation, Opioid-induced | |
| Submission type | Initial | |
| Date submission received | 2008-05-07 | |
| Status | Complete | |
| Date recommendation issued | 2009-01-28 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Zavesca | |
|---|---|---|
| Manufacturer | Actelion Pharmaceuticals Canada Inc. | |
| Indication | Gaucher disease | |
| Submission type | Initial | |
| Date submission received | 2004-05-13 | |
| Status | Complete | |
| Date recommendation issued | 2004-11-24 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Adderall XR | |
|---|---|---|
| Manufacturer | Shire Canada Inc. | |
| Indication | Attention deficit hyperactivity disorder, Adult | |
| Submission type | New Indication | |
| Date submission received | 2007-11-29 | |
| Status | Complete | |
| Date recommendation issued | 2008-06-25 | Recommendation and reasons |
| Recommendation | Do not list | |
| Plain language recommendation | Plain language recommendation | |
| Summary of CEDAC Discussion | Summary of CEDAC Discussion | |
| Overview of CDR reports | Overview of CDR reports | |
| Brand name | Adderall XR | |
|---|---|---|
| Manufacturer | Shire BioChem Inc. | |
| Indication | Attention deficit hyperactivity disorder | |
| Submission type | Resubmission #1 | |
| Date submission received | 2004-12-15 | |
| Status | Withdrawn |
| Brand name | Adderall XR | |
|---|---|---|
| Manufacturer | Shire BioChem Inc. | |
| Indication | Attention deficit hyperactivity disorder | |
| Submission type | Initial | |
| Date submission received | 2004-04-13 | |
| Status | Complete | |
| Date recommendation issued | 2004-11-24 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Myfortic | |
|---|---|---|
| Manufacturer | Novartis Pharmaceuticals Canada Inc. | |
| Indication | Prophylaxis of organ rejection in allogeneic renal transplants | |
| Submission type | Initial | |
| Date submission received | 2005-03-03 | |
| Status | Complete | |
| Date recommendation issued | 2005-07-08 | Recommendation and reasons |
| Recommendation | List in a similar manner to other drugs in class |
| Brand name | Tysabri | |
|---|---|---|
| Manufacturer | Biogen Idec Canada Inc. | |
| Indication | Multiple Sclerosis, relapsing-remitting | |
| Submission type | Resubmission #1 | |
| Date submission received | 2008-05-06 | |
| Status | Complete | |
| Date recommendation issued | 2009-02-25 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Tysabri | |
|---|---|---|
| Manufacturer | Biogen Idec Canada Inc. | |
| Indication | Multiple Sclerosis, relapsing-remitting | |
| Submission type | Initial | |
| Date submission received | 2006-10-26 | |
| Status | Complete | |
| Date recommendation issued | 2007-04-26 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Advicor | |
|---|---|---|
| Manufacturer | Oryx Pharmaceuticals Inc. | |
| Indication | Hypercholesterolemia and mixed dyslipidemia | |
| Submission type | Initial | |
| Date submission received | 2005-10-18 | |
| Status | Complete | |
| Date recommendation issued | 2006-04-26 | Recommendation and reasons |
| Recommendation | List |
| Brand name | Evra | |
|---|---|---|
| Manufacturer | Janssen-Ortho Inc. | |
| Indication | Contraceptive, patch | |
| Submission type | Initial | |
| Date submission received | 2003-12-19 | |
| Status | Complete | |
| Date recommendation issued | 2004-06-23 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Olmetec | |
|---|---|---|
| Manufacturer | Schering-Plough Canada Inc. | |
| Indication | Hypertension | |
| Submission type | Initial | |
| Date submission received | 2008-11-28 | |
| Status | Complete | |
| Date recommendation issued | 2009-05-27 | Recommendation and reasons |
| Recommendation | List in a similar manner to other drugs in class |
| Brand name | Olmetec Plus | |
|---|---|---|
| Manufacturer | Schering-Plough Canada Inc. | |
| Indication | Hypertension | |
| Submission type | Initial | |
| Date submission received | 2008-11-28 | |
| Status | Complete | |
| Date recommendation issued | 2009-05-27 | Recommendation and reasons |
| Recommendation | List in a similar manner to other drugs in class |
| Brand name | Xolair | |
|---|---|---|
| Manufacturer | Novartis Pharmaceuticals Canada Inc. | |
| Indication | Asthma, severe persistent | |
| Submission type | Resubmission #1 | |
| Date submission received | 2005-10-13 | |
| Status | Complete | |
| Date recommendation issued | 2006-03-07 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Xolair | |
|---|---|---|
| Manufacturer | Novartis Pharmaceuticals Canada Inc. | |
| Indication | Asthma, severe persistent | |
| Submission type | Initial | |
| Date submission received | 2005-04-18 | |
| Status | Suspended |
| Brand name | Invega | |
|---|---|---|
| Manufacturer | Janssen-Ortho Inc. | |
| Indication | Schizophrenia | |
| Submission type | Initial | |
| Date submission received | 2007-11-01 | |
| Status | Complete | |
| Date recommendation issued | 2008-05-28 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Invega Sustenna | |
|---|---|---|
| Manufacturer | Janssen-Ortho Inc. | |
| Indication | Schizophrenia | |
| Submission type | Initial | |
| Project Number | S0206 | |
| Date submission received | 2010-07-09 | |
| Patient input deadline | 2010-07-30 | |
| Status | Active | |
| Brand name | Pantoloc M | |
|---|---|---|
| Manufacturer | Altana Pharma Inc. | |
| Indication | Gastric acid secretion, reduction of | |
| Submission type | Initial | |
| Date submission received | 2006-03-17 | |
| Status | Complete | |
| Date recommendation issued | 2006-07-20 | Recommendation and reasons |
| Recommendation | List in a similar manner to other drugs in class |
| Brand name | Macugen | |
|---|---|---|
| Manufacturer | Pfizer Canada Inc. | |
| Indication | Macular degeneration, age-related | |
| Submission type | Initial | |
| Date submission received | 2005-10-20 | |
| Status | Complete | |
| Date recommendation issued | 2006-05-25 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Neulasta | |
|---|---|---|
| Manufacturer | Amgen Canada Inc. | |
| Indication | Neutropenia | |
| Submission type | Initial | |
| Date submission received | 2004-03-29 | |
| Status | Complete | |
| Date recommendation issued | 2004-10-27 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Pegasys RBV | |
|---|---|---|
| Manufacturer | Hoffman-La Roche Ltd. | |
| Indication | Hepatitis C, chronic | |
| Submission type | Initial | |
| Date submission received | 2004-05-14 | |
| Status | Complete | |
| Date recommendation issued | 2004-10-14 | Recommendation and reasons |
| Recommendation | List in a similar manner to other drugs in class |
| Brand name | Somavert | |
|---|---|---|
| Manufacturer | Pfizer Canada Inc. | |
| Indication | acromegaly | |
| Submission type | Initial | |
| Date submission received | 2006-01-25 | |
| Status | Complete | |
| Date recommendation issued | 2006-08-02 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Denavir | |
|---|---|---|
| Manufacturer | Novartis Consumer Health Care Inc. | |
| Indication | Herpes labialis (cold sores) | |
| Submission type | Initial | |
| Date submission received | 2006-09-20 | |
| Status | Complete | |
| Date recommendation issued | 2007-04-26 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Spriafil | |
|---|---|---|
| Manufacturer | Schering-Plough Canada Inc. | |
| Indication | Aspergillus and Candida infections | |
| Submission type | Initial | |
| Date submission received | 2007-05-24 | |
| Status | Complete | |
| Date recommendation issued | 2008-01-30 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Effient | |
|---|---|---|
| Manufacturer | Eli Lilly Canada Inc. | |
| Indication | Acute Coronary Syndrome (ACS) | |
| Submission type | Initial | |
| Date submission received | 2010-05-05 | |
| Status | Active |
| Brand name | Lyrica | |
|---|---|---|
| Manufacturer | Pfizer Canada Inc. | |
| Indication | diabetic peripheral neuropathy | |
| Submission type | Resubmission #1 | |
| Date submission received | 2009-03-20 | |
| Status | Complete | |
| Date recommendation issued | 2009-09-23 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Lyrica | |
|---|---|---|
| Manufacturer | Pfizer Canada Inc. | |
| Indication | Neuropathic pain | |
| Submission type | Initial | |
| Date submission received | 2005-06-27 | |
| Status | Complete | |
| Date recommendation issued | 2006-01-25 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Norprolac | |
|---|---|---|
| Manufacturer | Ferring Pharmaceuticals | |
| Indication | Hyperprolactinemia | |
| Submission type | Resubmission #1 | |
| Date submission received | 2005-11-23 | |
| Status | Complete | |
| Date recommendation issued | 2006-05-17 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Norprolac | |
|---|---|---|
| Manufacturer | Ferring Pharmaceuticals | |
| Indication | Hyperprolactinemia | |
| Submission type | Initial | |
| Date submission received | 2004-12-16 | |
| Status | Complete | |
| Date recommendation issued | 2005-09-28 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Isentress | |
|---|---|---|
| Manufacturer | Merck Frosst Canada Ltd. | |
| Indication | HIV (treatment naïve) | |
| Submission type | New Indication | |
| Date submission received | 2009-12-04 | |
| Status | Complete | |
| Date recommendation issued | 2010-06-23 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Isentress | |
|---|---|---|
| Manufacturer | Merck Frosst Canada Ltd. | |
| Indication | HIV | |
| Submission type | Initial | |
| Date submission received | 2007-11-29 | |
| Status | Complete | |
| Date recommendation issued | 2008-05-14 | Recommendation and reasons |
| Recommendation | List with criteria/condition | |
| Plain language recommendation | Plain language recommendation | |
| Summary of CEDAC Discussion | Summary of CEDAC Discussion | |
| Overview of CDR reports | Overview of CDR reports | |
| Brand name | Altace Plus Felodipine | |
|---|---|---|
| Manufacturer | Sanofi-Aventis Canada Inc. | |
| Indication | Hypertension | |
| Submission type | Initial | |
| Date submission received | 2006-06-22 | |
| Status | Complete | |
| Date recommendation issued | 2006-11-15 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Altace HCT | |
|---|---|---|
| Manufacturer | Sanofi-Aventis Canada Inc. | |
| Indication | Hypertension | |
| Submission type | Resubmission #1 | |
| Date submission received | 2007-03-26 | |
| Status | Complete | |
| Date recommendation issued | 2007-06-14 | Recommendation and reasons |
| Recommendation | List |
| Brand name | Altace HCT | |
|---|---|---|
| Manufacturer | Sanofi –Aventis Canada inc. | |
| Indication | Hypertension | |
| Submission type | Initial | |
| Date submission received | 2006-10-26 | |
| Status | Suspended |
| Brand name | Lucentis | |
|---|---|---|
| Manufacturer | Novartis Pharmaceuticals Inc. | |
| Indication | Macular degeneration, age-related | |
| Submission type | Initial | |
| Date submission received | 2007-07-12 | |
| Status | Complete | |
| Date recommendation issued | 2008-03-27 | Recommendation and reasons |
| Recommendation | List with criteria/condition | |
| Plain language recommendation | Plain language recommendation | |
| Summary of CEDAC Discussion | Summary of CEDAC Discussion | |
| Overview of CDR reports | Overview of CDR reports | |
| Brand name | Azilect | |
|---|---|---|
| Manufacturer | Teva Pharmaceuticals Industries Ltd. | |
| Indication | Parkinson’s disease | |
| Submission type | Request for Advice | |
| Date submission received | 2009-03-10 | |
| Status | Complete |
| Brand name | Azilect | |
|---|---|---|
| Manufacturer | Teva Neurosciences | |
| Indication | Parkinson's disease | |
| Submission type | Initial | |
| Date submission received | 2006-09-01 | |
| Status | Complete | |
| Date recommendation issued | 2007-03-28 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Rituxan | |
|---|---|---|
| Manufacturer | Hoffmann-La Roche Limited | |
| Indication | Arthritis, rheumatoid | |
| Submission type | Initial | |
| Date submission received | 2006-06-26 | |
| Status | Complete | |
| Date recommendation issued | 2007-02-14 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Xarelto | |
|---|---|---|
| Manufacturer | Bayer Inc. | |
| Indication | Venous thromboembolism prevention | |
| Submission type | Initial | |
| Date submission received | 2008-05-07 | |
| Status | Complete | |
| Date recommendation issued | 2008-12-17 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Exelon Patch | |
|---|---|---|
| Manufacturer | Novartis Pharmaceuticals Canada Inc. | |
| Indication | Dementia (Alzheimer's type) | |
| Submission type | Initial | |
| Date submission received | 2007-12-21 | |
| Status | Complete | |
| Date recommendation issued | 2008-07-23 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Nplate | |
|---|---|---|
| Manufacturer | Amgen Canada Inc. | |
| Indication | Chronic immune (idiopathic) thrombocytopenic purpura (ITP) | |
| Submission type | Initial | |
| Date submission received | 2009-09-29 | |
| Status | Complete | |
| Date recommendation issued | 2010-05-27 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Kuvan | |
|---|---|---|
| Manufacturer | BioMarin Pharmaceutical Canada Inc. | |
| Indication | Phenylketonuria (PKU). | |
| Submission type | Initial | |
| Project Number | S0205 | |
| Date submission received | 2010-07-08 | |
| Patient input deadline | 2010-07-29 | |
| Status | Active | |
| Brand name | Onglyza | |
|---|---|---|
| Manufacturer | Bristol-Myers Squibb Canada | |
| Indication | Diabetes Mellitus (Type 2) | |
| Submission type | Initial | |
| Date submission received | 2009-11-09 | |
| Status | Complete | |
| Date recommendation issued | 2010-06-17 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Revatio | |
|---|---|---|
| Manufacturer | Pfizer Canada Inc. | |
| Indication | Pulmonary arterial hypertension (WHO class II and III) | |
| Submission type | Initial | |
| Date submission received | 2006-09-20 | |
| Status | Complete | |
| Date recommendation issued | 2007-02-14 | Recommendation and reasons |
| Recommendation | List in a similar manner |
| Brand name | Januvia | |
|---|---|---|
| Manufacturer | Merck Frosst Canada Ltd. | |
| Indication | Diabetes Mellitus (Type 2) | |
| Submission type | Resubmission #1 | |
| Date submission received | 2009-10-29 | |
| Status | Complete | |
| Date recommendation issued | 2010-06-23 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Januvia | |
|---|---|---|
| Manufacturer | Merck Frosst Canada Ltd. | |
| Indication | Diabetes Mellitus (Type 2) | |
| Submission type | Initial | |
| Date submission received | 2007-12-20 | |
| Status | Complete | |
| Date recommendation issued | 2008-06-18 | Recommendation and reasons |
| Recommendation | Do not list | |
| Plain language recommendation | Plain language recommendation | |
| Summary of CEDAC Discussion | Summary of CEDAC Discussion | |
| Overview of CDR reports | Overview of CDR reports | |
| Brand name | Janumet | |
|---|---|---|
| Manufacturer | Merck Frosst Canada Ltd. | |
| Indication | Diabetes Mellitus (Type 2) | |
| Submission type | Initial | |
| Date submission received | 2009-11-04 | |
| Status | Complete | |
| Date recommendation issued | 2010-06-23 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Thelin | |
|---|---|---|
| Manufacturer | Encysive Canada Inc. | |
| Indication | Pulmonary arterial hypertension (WHO class II and III) | |
| Submission type | Resubmission #1 | |
| Date submission received | 2008-05-05 | |
| Status | Complete | |
| Date recommendation issued | 2009-01-28 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Thelin | |
|---|---|---|
| Manufacturer | Encysive Canada Inc. | |
| Indication | Pulmonary arterial hypertension (WHO class II and III) | |
| Submission type | Initial | |
| Date submission received | 2007-06-22 | |
| Status | Complete | |
| Date recommendation issued | 2008-01-30 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Xyrem | |
|---|---|---|
| Manufacturer | Valeant Canada Ltd. | |
| Indication | Narcolepsy | |
| Submission type | Resubmission #1 | |
| Date submission received | 2008-07-09 | |
| Status | Complete | |
| Date recommendation issued | 2009-01-28 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Xyrem | |
|---|---|---|
| Manufacturer | Valeant Canada Ltd. | |
| Indication | Narcolepsy | |
| Submission type | Initial | |
| Date submission received | 2007-08-29 | |
| Status | Withdrawn |
| Brand name | Vesicare | |
|---|---|---|
| Manufacturer | Astellas Pharma Canada Inc. | |
| Indication | Bladder, overactive | |
| Submission type | Resubmission #1 | |
| Date submission received | 2009-01-05 | |
| Status | Complete | |
| Date recommendation issued | 2009-06-17 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Vesicare | |
|---|---|---|
| Manufacturer | Astellas Pharma Canada Inc. | |
| Indication | Bladder, overactive | |
| Submission type | Initial | |
| Date submission received | 2006-07-24 | |
| Status | Complete | |
| Date recommendation issued | 2007-01-24 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Omnitrope | |
|---|---|---|
| Manufacturer | Sandoz Canada Inc. | |
| Indication | Growth hormone deficiency in children and adults | |
| Submission type | Initial | |
| Date submission received | 2009-06-12 | |
| Status | Complete | |
| Date advice issued | 2009-12-16 | Advice - SEB |
| Brand name | Nexavar | |
|---|---|---|
| Manufacturer | Bayer Inc. | |
| Indication | Renal cell carcinoma | |
| Submission type | Initial | |
| Date submission received | 2006-07-31 | |
| Status | Complete | |
| Date recommendation issued | 2007-02-28 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Sutent | |
|---|---|---|
| Manufacturer | Pfizer Canada Inc. | |
| Indication | Gastrointestinal stromal tumour (GIST) | |
| Submission type | Initial | |
| Date submission received | 2006-07-20 | |
| Status | Complete | |
| Date recommendation issued | 2007-03-28 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Sutent | |
|---|---|---|
| Manufacturer | Pfizer Canada Inc. | |
| Indication | Metastatic renal cell carcinoma | |
| Submission type | Resubmission #1 | |
| Date submission received | 2006-09-20 | |
| Status | Complete | |
| Date recommendation issued | 2007-04-26 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Adcirca | |
|---|---|---|
| Manufacturer | Eli Lilly Canada Inc. | |
| Indication | Pulmonary Arterial Hypertension | |
| Submission type | Initial | |
| Date submission received | 2010-02-05 | |
| Status | Complete | |
| Date recommendation issued | 2010-07-15 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Sebivo | |
|---|---|---|
| Manufacturer | Novartis Pharmaceuticals Canada Inc. | |
| Indication | Hepatitis B (chronic) | |
| Submission type | Initial | |
| Date submission received | 2006-12-04 | |
| Status | Complete | |
| Date recommendation issued | 2007-09-26 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Twynsta | |
|---|---|---|
| Manufacturer | Boehringer Ingelheim (Canada) Ltd | |
| Indication | Essential Hypertension | |
| Submission type | Pre-NOC | |
| Project Number | S0207 | |
| Date submission received | 2010-07-09 | |
| Patient input deadline | 2010-07-30 | |
| Status | Active | |
| Brand name | Viread | |
|---|---|---|
| Manufacturer | Gilead Sciences Canada Inc. | |
| Indication | Hepatitis B (Chronic) | |
| Submission type | New Indication | |
| Date submission received | 2008-10-02 | |
| Status | Complete | |
| Date recommendation issued | 2009-03-18 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Viread | |
|---|---|---|
| Manufacturer | Gilead Sciences Canada Inc. | |
| Indication | HIV infection | |
| Submission type | Request for Advice | |
| Date submission received | 2008-07-07 | |
| Status | Complete |
| Brand name | Viread | |
|---|---|---|
| Manufacturer | Gilead Sciences Canada Inc. | |
| Indication | HIV infection | |
| Submission type | Resubmission #1 | |
| Date submission received | 2005-08-11 | |
| Status | Complete | |
| Date recommendation issued | 2006-03-15 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Viread | |
|---|---|---|
| Manufacturer | Gilead Sciences Canada Inc. | |
| Indication | HIV infection | |
| Submission type | Initial | |
| Date submission received | 2004-02-23 | |
| Status | Complete | |
| Date recommendation issued | 2004-08-25 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Forteo | |
|---|---|---|
| Manufacturer | Eli Lilly Canada Inc. | |
| Indication | Severe osteoporosis in women | |
| Submission type | ACP Submission | |
| Date submission received | 2009-10-23 | |
| Status | Complete | |
| Date recommendation issued | 2010-03-17 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Forteo | |
|---|---|---|
| Manufacturer | Eli Lilly Canada Inc. | |
| Indication | Osteoporosis | |
| Submission type | Resubmission #3 | |
| Date submission received | 2009-06-12 | |
| Status | Withdrawn |
| Brand name | Forteo | |
|---|---|---|
| Manufacturer | Eli Lilly Canada Inc. | |
| Indication | Osteoporosis (glucocorticoid induced) | |
| Submission type | New Indication | |
| Date submission received | 2008-12-18 | |
| Status | Complete | |
| Date recommendation issued | 2009-07-22 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Forteo | |
|---|---|---|
| Manufacturer | Eli Lilly Canada Inc. | |
| Indication | Osteoporosis | |
| Submission type | Resubmission #2 | |
| Date submission received | 2008-12-18 | |
| Status | Withdrawn |
| Brand name | Forteo | |
|---|---|---|
| Manufacturer | Eli Lilly Canada Inc. | |
| Indication | Osteoporosis | |
| Submission type | Resubmission #1 | |
| Date submission received | 2006-05-29 | |
| Status | Withdrawn |
| Brand name | Forteo | |
|---|---|---|
| Manufacturer | Eli Lilly Canada Inc. | |
| Indication | Osteoporosis | |
| Submission type | Initial | |
| Date submission received | 2004-06-08 | |
| Status | Complete | |
| Date recommendation issued | 2004-12-22 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Brilinta | |
|---|---|---|
| Manufacturer | AstraZeneca Canada Inc | |
| Indication | Acute Coronary Syndromes (ACS) | |
| Submission type | Pre-NOC - Initial | |
| Project Number | S0203 | |
| Date submission received | 2010-06-08 | |
| Patient input deadline | 2010-06-30 | |
| Status | Active | |
| Brand name | Aptivus | |
|---|---|---|
| Manufacturer | Boehringer Ingelheim (Canada) Inc. | |
| Indication | HIV infection | |
| Submission type | Initial | |
| Date submission received | 2005-12-15 | |
| Status | Complete | |
| Date recommendation issued | 2006-05-17 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Actemra | |
|---|---|---|
| Manufacturer | Hoffmann-La Roche Limited | |
| Indication | Arthritis, Rheumatoid | |
| Submission type | Initial | |
| Project Number | S0201 | |
| Date submission received | 2010-05-27 | |
| Patient input deadline | 2010-06-17 | |
| Status | Active | |
| Brand name | Tridural | |
|---|---|---|
| Manufacturer | Labopharm Inc. | |
| Indication | Pain | |
| Submission type | Initial | |
| Date submission received | 2007-11-29 | |
| Status | Complete | |
| Date recommendation issued | 2008-04-17 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Ralivia | |
|---|---|---|
| Manufacturer | Biovail Pharmaceuticals Canada | |
| Indication | Pain | |
| Submission type | Initial | |
| Date submission received | 2007-10-29 | |
| Status | Complete | |
| Date recommendation issued | 2008-06-25 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Zytram XL | |
|---|---|---|
| Manufacturer | Purdue Pharma | |
| Indication | Pain | |
| Submission type | Resubmission #1 | |
| Date submission received | 2007-03-15 | |
| Status | Complete | |
| Date recommendation issued | 2007-09-26 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Zytram XL | |
|---|---|---|
| Manufacturer | Purdue Pharma | |
| Indication | Acute pain | |
| Submission type | Initial | |
| Date submission received | 2006-11-03 | |
| Status | Withdrawn |
| Brand name | Tramacet | |
|---|---|---|
| Manufacturer | Janssen-Ortho Inc. | |
| Indication | Acute pain | |
| Submission type | Initial | |
| Date submission received | 2006-10-02 | |
| Status | Complete | |
| Date recommendation issued | 2007-05-17 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | DuoTrav | |
|---|---|---|
| Manufacturer | Alcon Canada Inc. | |
| Indication | Glaucoma | |
| Submission type | Initial | |
| Date submission received | 2006-03-24 | |
| Status | Complete | |
| Date recommendation issued | 2006-08-24 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Remodulin | |
|---|---|---|
| Manufacturer | Northern Therapeutics Inc. | |
| Indication | Pulmonary arterial hypertension (NYHA Class III and IV patients) | |
| Submission type | Resubmission #1 | |
| Date submission received | 2006-02-24 | |
| Status | Complete | |
| Date recommendation issued | 2006-07-20 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Remodulin | |
|---|---|---|
| Manufacturer | Northern Therapeutics Inc. | |
| Indication | Pulmonary arterial hypertension (NYHA Class III and IV patients) | |
| Submission type | Initial | |
| Date submission received | 2004-07-14 | |
| Status | Complete | |
| Date recommendation issued | 2004-11-17 | Recommendation and reasons |
| Recommendation | Do not list |
| Brand name | Trelstar | |
|---|---|---|
| Manufacturer | Watson Laboratories Inc. | |
| Indication | Prostate cancer | |
| Submission type | Initial | |
| Date submission received | 2006-02-27 | |
| Status | Complete | |
| Date recommendation issued | 2006-07-20 | Recommendation and reasons |
| Recommendation | List in a similar manner to other drugs in class |
| Brand name | Trosec | |
|---|---|---|
| Manufacturer | Oryx Pharmaceuticals Inc. | |
| Indication | Bladder, overactive | |
| Submission type | Initial | |
| Date submission received | 2006-03-24 | |
| Status | Complete | |
| Date recommendation issued | 2006-08-24 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Stelara | |
|---|---|---|
| Manufacturer | Janssen-Ortho Inc. | |
| Indication | Psoriasis | |
| Submission type | Initial | |
| Date submission received | 2009-01-07 | |
| Status | Complete | |
| Date recommendation issued | 2009-06-17 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Champix | |
|---|---|---|
| Manufacturer | Pfizer Canada Inc. | |
| Indication | Smoking-cessation | |
| Submission type | Initial | |
| Date submission received | 2007-03-21 | |
| Status | Complete | |
| Date recommendation issued | 2007-08-16 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | VFEND | |
|---|---|---|
| Manufacturer | Pfizer Canada Inc. | |
| Indication | Candidemia | |
| Submission type | Resubmission #2 | |
| Date submission received | 2006-03-24 | |
| Status | Complete | |
| Date recommendation issued | 2006-10-25 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | VFEND | |
|---|---|---|
| Manufacturer | Pfizer Canada Inc. | |
| Indication | Aspergillosis, invasive | |
| Submission type | Resubmission #1 | |
| Date submission received | 2004-10-25 | |
| Status | Complete | |
| Date recommendation issued | 2005-04-14 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | VFEND | |
|---|---|---|
| Manufacturer | Pfizer Canada Inc. | |
| Indication | Aspergillosis, Invasive | |
| Submission type | Initial | |
| Date submission received | 2004-08-24 | |
| Status | Withdrawn |
| Brand name | Zeldox | |
|---|---|---|
| Manufacturer | Pfizer Canada Inc. | |
| Indication | Schizophrenia and related psychotic disorders | |
| Submission type | Initial | |
| Date submission received | 2008-01-10 | |
| Status | Complete | |
| Date recommendation issued | 2008-08-14 | Recommendation and reasons |
| Recommendation | List with criteria/condition |
| Brand name | Aclasta | |
|---|---|---|
| Manufacturer | Novartis Pharmaceuticals Canada Inc. | |
| Indication | Osteoporosis (postmenopausal women) | |
| Submission type | Initial | |
| Date submission received | 2007-11-29 | |
| Status | Complete | |
| Date recommendation issued | 2008-06-25 | Recommendation and reasons |
| Recommendation | Do not list |