Canadian Pharmaceutical Spending: 50% of the cost for 2% of the population
In Canada, public drug program spending exceeded approximately $20 billion in 2024, and total pharmaceutical expenditures approaching $40 billion annually when private insurance, hospital medications, and cancer therapies are included.1 Historically, medication spending was driven primarily by the number of users. Increasingly, however, costs are being driven by a small number of high-cost medications. Approximately 50% of public drug spending is now attributable to about 2% of patients receiving medications costing more than $10,000 annually.1 Biologics alone account for nearly 30% of public drug spending in Canada.1,2
At the same time, some commonly prescribed medication classes are becoming more affordable through generic competition and biosimilar availability. For example, many chronic disease medications are expected to decrease substantially in price over the coming years. However, rapid uptake of newer expensive medications — particularly GLP-1 receptor agonists such as semaglutide — continues to drive major increases in drug spending. Canadian total (public and private) spending on semaglutide is around $2 billion annually.2 Generic semaglutide was approved in Canada in April 2026 and use could potentially save hundreds of millions of dollars annually.
Canada has one of the lowest rates of biosimilar uptake among OECD countries.1,3 Evidence demonstrates that biosimilars provide similar clinical outcomes and safety compared with originator products.4,5 British Columbia leads all provinces in their biosimilar initiatives, saving $730 million over five years without increasing healthcare utilization or adverse patient outcomes.6,7
Similarly, evidence suggests that in several therapeutic areas, lower-cost medications within a class provide comparable patient-oriented outcomes to substantially more expensive alternatives.
Examples of evidence and cost informed prescribing for primary care practitioners include:
In addition to selecting lower-cost therapeutic alternatives, other strategies to reduce medication expenditures include:
Canada remains the only OECD country with universal healthcare coverage that does not yet provide universal pharmacare coverage for outpatient prescription medications. In 2024, the federal Pharmacare Act initiated limited national coverage for diabetes medications and supplies, oral contraceptives, and some menopause hormone therapies in participating provinces and territories.11 While a few provinces have signed onto this initiative, broader implementation of the national pharmacare programs could substantially reduce drug expenditures and improving medication access.
In Alberta, several commonly used medication classes — including ACE inhibitors, ARBs, calcium channel blockers, statins, and proton pump inhibitors — are subject to maximal allowable cost (MAC) pricing policies. Additional information regarding Alberta’s MAC pricing and biosimilar initiatives can be found through Alberta Blue Cross and provincial formulary resources.
We are pleased to provide the updated Price Comparison of Commonly Prescribed Pharmaceuticals in Alberta for 2026. We encourage prescribers to consider medication cost, formulary coverage, and evidence for patient-oriented outcomes when selecting therapies — particularly when choosing among therapeutically similar medications.
1Canadian Institute for Health Information (CIHI): National health expenditure trends. Available: https://www.cihi.ca/en/national-health-expenditure-trends. Accessed April 25, 2026.
2Tadrous M, Wang KZ, Chaudhry S et al. Canadian Trends in Estimated Drug Purchases and Projections: 2024 and 2025. Canadian Journal of Health Technologies CDA-AMC: 2024; 4 (12).
3Zhang Y. Canada’s evolving market for biosimilars and what it means for payers. Patented Medicine Prices Review Board, National Prescription Drug Utilization Information System (NPDUIS). Available at: https://www.canada.ca/en/patented-medicine-prices-review/services/npduis/analytical-studies/posters/biosimilars-2025poster.html. Accessed April 27, 2026.
4Herndon TM, Ausin C. Brahme NN. Safety outcomes when swithing between biosimilars and reference biologics: A systematic review and meta-analysis. PLoS ONE 2023; 18(10): e0292231.
5Perry D, Ton J, Kolber MR. Tools for Practice # 236, May 27, 2019.
6McClean AR, Law MR, Harrison M et al. Uptake of biosimilar drugs in Canada: analysis of provincial policies and usage data. CMAJ. 2022;194(15):e556-560.
7British Columbia Ministry of Health. B.C.’s Biosimilars Initiative: A Report on Patient and Financial Impact. Available at: https://news.gov.bc.ca/files/BCBiosimilarsInitiativeAReportonPatientandFinancialImpact_June%202024.pdf. Accessed April 25, 2026.
8Dugre N, McCormack J, Nickonchuk T, Kolber MR. Tools for Practice #412, Apr 20, 2026. Available at: https://cfpclearn.ca/tfp412.
9Moe S. Allan GM, Tools for Practice #250, Jan 6, 2020. Available at: https://cfpclearn.ca/tfp250.
10Zinman B, Wanner C, Lachin JM et al. Empagliflozin, Cardiovascular Outcomes, and Mortality in Type 2 Diabetes. N Engl J Med 2015;373:2117-28.
11Government of Canada. National Pharmacare. Available at: https://www.canada.ca/en/health-canada/services/health-services-benefits/national-pharmacare.html. Accessed Apr 27, 2026.