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PLOS ONE logoLink to PLOS ONE
. 2023 Mar 23;18(3):e0271079. doi: 10.1371/journal.pone.0271079

Lessons from 20 years of medical cannabis use in Canada

Minsup Shim 1, Hai Nguyen 2, Paul Grootendorst 1,3,*
Editor: Julian Aherne4
PMCID: PMC10035846  PMID: 36952564

Abstract

Background

Canada was one of the first countries to regulate the medical use of cannabis. However, literature on Canada’s medical cannabis program is limited.

Methods

We use administrative data from the medical cannabis program, and licensed cannabis vendor catalog data to describe a) the participation of patients, physicians, and cannabis vendors in the program from its inception in 1999 to 2021, and b) trends in medical cannabis consumption, prices and potency. We also use national surveys conducted over the last several decades to estimate trends in regular cannabis use (medical or otherwise) and how it changed during the medical cannabis access regimes.

Results

In 2001, the Canadian government granted access to those with physician-documented evidence of a severe health problem that could not be managed using conventional therapies. Most patients accessed cannabis grown under a personal production license. By 2013, authorized daily cannabis dosages were very high. In 2014, the government, concerned over illegal diversion, required that cannabis be purchased from a licensed commercial grower; personal production was banned. Physicians were given responsibility for authorizing patient access. To fill the regulatory void, the physician regulatory bodies in Canada imposed their own prescribing restrictions. After these changes, the number of physicians who were willing to support patient cannabis use markedly decline but the number of patients participating in the program sharply increased. Medical cannabis use varied by province–rates were generally lower in provinces with stricter regulations on physician cannabis prescribing. Most varieties of cannabis oil available for sale are now high in CBD and low in THC. Dry cannabis varieties, conversely, tend to be high in THC and low in CBD. Inflation adjusted prices of most varieties of medical cannabis have declined over time. We find that rates of daily cannabis use (medical or otherwise) increased markedly after the 2014 policy regime. The fraction of Canadians using cannabis daily increased again after the 2018 legalization of recreational cannabis; at the same time, participation in the medical access program declined.

Conclusion

The implications for patient health outcomes of changes in the medical cannabis program and legalization of recreational use remains an important area for future research.

Introduction

Canada introduced a medical cannabis access program in 1999, making it one of the first countries to do so. The regulations that govern patient eligibility and the legal sources of supply, however, have evolved over time. These changes have broadened patient eligibility criteria, made it easier for patients to obtain authorization, and created a regulated domestic cannabis industry which offers a large range of products that vary in both potency and dosage forms. In this paper, we provide descriptive evidence on the participation of physicians, patients and cannabis vendors in the Canadian medical cannabis access regime over the last two decades. As far as we are aware, we are the first to do so.

We begin by outlining the history of Canada’s medical cannabis access regime. Next, we present empirical evidence on national trends in patient and physician participation in the medical cannabis regime. We also examine trends in the prices and varieties of medical cannabis for sale by authorized vendors, known as Licensed Producers. We then examine provincial trends in the volume of medical cannabis sold by Licensed Producers and explore possible reasons for the interprovincial variation. One such reason is the degree of restrictiveness of province-specific regulations on physician cannabis prescribing. Next, we use repeated cross sectional national level surveys to examine the possible effects of the liberalization of the medical cannabis access system on overall rates of regular cannabis use (medical or otherwise) in the community.

The plan of the paper is as follows. In the following section we briefly describe Canada’s cannabis access policy over the last two decades. Next, we present the data used to describe various aspects of the program. We then present results and finally discuss results.

Canada’s Medical Cannabis Regulatory Policy, 1999–2021

Prior to 2001, severely ill patients could petition the federal Minister of Health for an exemption from the Controlled Drugs and Substances Act (CDSA); the CDSA prohibits or regulates the use of cannabis, opiates, and other drugs [1]. This ministerial exemption, codified in Section 56 of the CDSA, was unused until the Ontario Superior Court instructed Health Canada (the federal Ministry of Health) to liberalize medical cannabis access [2]. In response, the Minister granted authorization, on compassionate grounds, to two individuals who were living with HIV/AIDS [2]; these individuals were allowed to cultivate their own cannabis [3].

These regulations were overturned by the courts in 2000. A man who had experienced severe epilepsy since childhood, Terrance Parker, found that smoking cannabis was more effective than conventional medicines in reducing the frequency of debilitating seizures. He cultivated and used cannabis without ministerial approval and, in 1996, was charged under the CDSA. Parker prevailed at trial; the crown appealed and the court again ruled in favor of Parker. Moreover, the appeals court found that the arbitrariness of the Section 56 exemption breached patients’ constitutional right to life, liberty, and security [4].

Health Canada duly promulgated the Marihuana Medical Access Regulations (MMAR) in 2001. Patients were required to apply to Health Canada for authorization to possess cannabis; the 29 page application required inter alia written documentation from the patient’s primary physician (and in some cases a physician specialist as well) that the patient was either receiving palliative care or was experiencing debilitating symptoms related to specific medical conditions or treatments, such as severe nausea from chemotherapy, that could not be treated using conventional pharmaceuticals [2]. The first patients were enrolled in the program in early 2003.

Under the MMAR, authorized patients or their designates could obtain a license to grow cannabis plants; patients could also purchase dried cannabis from Health Canada at $5 per gram. These production licenses stipulated the number of cannabis plants allowed; this was determined formulaically from the authorized daily consumption and an estimated average yield per cannabis plant [5].

By December 2013, the average authorized daily consumption under the MMAR was about 18 grams. A person authorized to consume 18 grams daily was allowed to grow 88 cannabis plants [1]. A delegated producer could grow cannabis on behalf of 4 authorized users; thus a delegated production facility could contain several hundred plants [1]. Authorities grew concerned about both the safety of residential cannabis cultivation [6] and the diversion of cannabis to the illicit market [1]. These concerns were especially pronounced in the province of British Columbia. In that province, over 2 million cannabis plants were authorized under the MMAR.

In response to these concerns, Health Canada replaced the MMAR with a new set of regulations known as the Marihuana for Medical Purposes Regulations (MMPR). The MMPR, introduced in late 2013 and fully enacted on April 1, 2014, revoked the cannabis production licenses. Authorized patients could obtain cannabis (in dried form only) via mail order from a Licensed Producer, a commercial vendor approved and regulated by Health Canada.

The second goal of the MMPR was to remove Health Canada from the business of authorizing patient access to medical cannabis. Health Canada delegated this responsibility to physicians and nurse practitioners, who could authorize cannabis use through a one-page prescription-like form called a “medical document”. Health Canada did not regulate the potency or daily consumption of cannabis, although it did set a possession limit of 150 grams. To fill the regulatory void [79], each provincial College of Physicians and Surgeons (hereafter, the “Colleges”) imposed their own prescribing restrictions. (These Colleges, which are responsible for licensing, disciplining, and regulating physicians, are the provincial equivalents to state medical boards in the United States.) The cannabis prescribing rules varied by province and include inter alia requirements that the physician meet with the patient at least every 3 months, assess patient addiction risk, and in Quebec, enroll the patient into a research study on cannabis use [10]. None of the authorities that regulate nurse practitioners have allowed cannabis prescribing.

Patient groups, in turn, successfully petitioned the courts to allow the sale of cannabis oil and fresh cannabis leaves (in 2015) [11] and again allow patients (or their designates) to cultivate cannabis for personal use (in August 2016) albeit with more restrictions than under the MMAR. The revised set of rules are known as the Access to Cannabis for Medical Purposes Regulations (ACMPR) [12, 13].

More recently, in October 2018, Canada legalized the recreational use of cannabis for those aged 19 and older. Canada was only the second country, after Uruguay, to do so. As before, only Licensed Producers are eligible to produce cannabis commercially although individuals are allowed to grow a limited number of cannabis plants for personal use. Each province has authority over i) cannabis use, including age restrictions on users and locations that cannabis can be consumed; ii) retail sales formats; iii) excise taxes levied on cannabis sales; and finally, iv) the regulations governing cultivation for personal use. Recreational cannabis sales are subject to both federal and provincial excise and sales taxes. Controversially, these taxes also apply to medical cannabis use. Fig 1 summarizes the timeline of medical and non-medical cannabis access regimes.

Fig 1. Timeline of medical and recreational cannabis access regimes in Canada.

Fig 1

Note: MMAR: Marihuana Medical Access Regulations. MMPR: Marihuana for Medical Purposes Regulations. ACMPR: Access to Cannabis for Medical Purposes Regulations.

Methods

We collected data that reflect physician and patient participation in the medical cannabis program, the prices and potency of medical cannabis sold by Licensed Producers, rates of medical cannabis use and the fraction of the population using cannabis regularly over time.

Information on the MMAR regime came from Health Canada administrative records and affidavits of a Health Canada employee [1, 14] in a Federal Court challenge over the constitutionality of the MMPR regime [15]. Health Canada provided data on the number of patients authorized to possess cannabis, by province and month, and the number of physicians supporting these cannabis possession applications nationally, by month. The affidavits contained data on the number of personal and delegated cannabis production licenses [14], and the number of cannabis plants authorized [1], by province, in December 2013. We expressed these data as rates per 100,000 population age 20+ using Statistics Canada provincial population estimates for July 2013 [16]. Some of the Health Canada administrative data we relied on are also available online [17, 18].

National data on the number of individuals authorized to possess cannabis, the number of production licenses, and permitted daily dosages, annually, from 2001–2014 were reported in an affidavit [14]. Daily dosages were reported in 18 irregularly spaced intervals, starting at 0 to 2.9 grams, then 3.0 to 4.9 grams, up to 250 to 299.9 grams. (Only 1 individual was authorized to use over 300 grams daily.) We used these data to estimate, by year, the average authorized daily dose; this is the weighted average of the interval midpoints, where the interval weights were the fraction of patients authorized to use the quantity of cannabis in the interval.

Health Canada also provided, for the MMPR/ACMPR regimes, data on the number of medical cannabis mail order shipments from Licensed Producers to authorized patients, by province and month. We expressed shipments as rates per 1,000 population, using Statistics Canada quarterly province-level population estimates [19].

Health Canada also provided data on the quantity of cannabis sold by Licensed Producers nationally, by presentation (dry vs oil) and month from May 2014 to September 2019. Dry cannabis includes “any part of a cannabis plant, except seeds, that has been through a drying process (dried flowers, pre-ground/milled (trim/shake), pre-rolls)” [20]. Oils are “made using extraction processing methods or by synthesizing phytocannabinoids and intended for inhalation or ingestion, including by absorption in the mouth or other routes of administration (e.g. vape pens, hash, tinctures, softgels, suppositories)” [20]. Dry cannabis is normally smoked and sometimes vaped, while oils are used primarily for vaping. Product sales were measured in kilograms until September 2018; afterwards cannabis oil was measured in litres. As a litre of oil weighs less than a kilogram, this measure change will cause unit oil sales to be modestly overstated.

Starting October 2019, Health Canada changed the way it reported Licensed Producer product sales. Sales volumes were measured in “packaged units” sold to patients, cannabis oil was relabelled as “cannabis extracts” and sales of cannabis “edibles” (which include cannabis-infused beverages, and foods such as gummies and chocolates) were reported. These data were obtained from the Government of Canada “Open Government” website [20].

We examined the impact on interprovincial rates of medical cannabis use of the number and type of cannabis prescribing restrictions imposed by each provincial College. To do so we surveyed these restrictions during April 2016 and assigned each restriction a score from 0.5 to 4, with larger values representing more onerous restrictions. For instance, the requirement that the prescriber meet with the patient in person to prescribe cannabis was assigned a score of 1. The requirement that the prescriber be the patient’s primary physician was assigned a score of 3. These requirements were independently rated by two of the investigators and differences resolved via consensus. We then summed the scores to generate, for each province, a composite cannabis prescribing restriction score. These scores were plotted against province-level data on medical cannabis use. This was measured as the average number of cannabis shipments from Licensed Producers to registered clients over the three-month period March to May 2016. Rates were expressed as shipments per 100,000 population using the quarterly Statistics Canada population estimates [21].

We also investigated the association between the provincial restrictions on physician cannabis prescribing and the fraction of regular cannabis users (those who use cannabis weekly or daily) aged 20 and older who are enrolled in the medical cannabis program. This fraction was estimated as the ratio of the number of individuals enrolled in the medical access program in July 2015 to the number of regular users, estimated from the public use version of the 2015 Statistics Canada Canadian Tobacco, Alcohol and Drugs Survey. Presumably, the more stringent the regulations, the greater the fraction of regular users who obtain cannabis outside of the medical program.

To infer trends in the prices and potency of prescribed dry and oil-based cannabis under the MMPR/ACMPR regimes, we extracted data from the on-line product catalogs of Licensed Producers at the start of each month from June 2016 to December 2022 (except for December 2019). We excluded “micro-licence holders”, Licensed Producers that are limited to a maximum of 200 square metres of growing surface. Despite comprising 38% of all federal licence holders by July 31, 2022, they accounted for less than 1% of LP sales [22].

We recorded the concentrations of the two primary active ingredients, tetrahydrocannabinol (THC) and cannabidiol (CBD) and the Canadian dollar price per gram (dried cannabis) or the price per ml (oil) for each product on offer. Products were assigned to one of four categories based on the strength of THC and CBD: THC≥10% and CBD≥10%; THC≥10% and CBD<10%; THC<10% and CBD≥10%; and THC<10% and CBD<10%. We calculated the average price of products, by strength category, month, and type of cannabis presentation (dry vs oil). We divided by the Statistics Canada all-item consumer price index (CPI) to adjust for inflation [23]. We did not collect pricing data for other types of cannabis products on offer, such as skin creams and other topicals or cannabis infused teas, chocolates and other types of edible cannabis.

These pricing data have some limitations. First, a referee notes that Licensed Producer reported concentrations of THC and CBD per ml of oil-based cannabis products can diverge from actual concentrations. This may introduce some error when estimating the price per unit of THC or CBD contained in the product. Second, to calculate average prices, ideally, we would weight the prices by the market share of the Licensed Producer selling the product, but Licensed Producer specific sales data are not publicly available. Third, some Licensed Producer pricing data was not available on-line; in some cases, on-line access was restricted to registered users.

To assess our price data, we compared our data with monthly Statistics Canada national “medicinal cannabis” CPI data from January 2019 to October 2022 [23]. These data are a weighted average of consumer price indices for both dry and oil forms [24]; each of the price indices are based on a sample of products [25]. Statistics Canada’s publications do not disclose the weights in this weighted average or how cannabis product sampling was conducted.

We calculated the strength category specific share of all products on offer, by month, and type of cannabis presentation. We then graphed these data to illustrate trends in the potency of medical cannabis on offer. These graphs reflect trends in the potency of medical cannabis being used if the number of products in a strength category is proportional to the level of patient demand for all products in the category.

We next examined province-level trends in rates of regular cannabis use over the period 1989 to 2021 to assess possible impacts of the introduction of the medical cannabis access system in 2003 and its liberalization in 2013. To do so, we assembled the national health and drug use surveys conducted over this period and estimated the fraction of the residential population aged 20 and older that consumes cannabis daily or almost daily. These estimates were stratified by survey, year and province. Next, for each province, we fit a median spline curve with 9 bands to these year and survey-specific estimates to discern local trends. We use the public use versions of the 1989 National Alcohol and Drugs Survey; 1994 Canada’s Alcohol and Other Drugs Survey; 2002 Canadian Community Health Survey; 2004 Canadian Addiction Survey (CAS); 2005–2013 Canadian Tobacco Use Monitoring Surveys; 2008–2012 Canadian Alcohol and Drug Use Monitoring Surveys (CADUMS); the 2013, 2015, 2017 Canadian Tobacco, Alcohol and Drugs Survey; the 2019–2021 Canadian Tobacco and Nicotine Survey; and the 2018, 2019 and 2020 National Cannabis Survey (NCS). All surveys were conducted by Statistics Canada except for the CAS, CADUMS and NCS; these were commissioned by Health Canada and conducted by private sector firms.

All these surveys used telephone interviews of provincial households with land-based telephones. Households were selected using random-digit dialing and questionnaires were administered to a randomly selected household member, age 15 or older, using Computer Assisted Telephone Interviewing. The NCS was the exception; households were selected using random-digit dialing of both land and cell phone numbers. Screening questions were asked over the phone and eligible individuals were invited to complete an on-line survey.

Households from the smaller provinces, and younger individuals were oversampled. The surveys include observation specific weights that adjust for household non-response and other factors that make population estimates consistent with known province-age-sex totals. We use these survey weights when estimating the proportion of the residential population aged 20+ that use cannabis regularly. The median number of observations per estimate was over 1,200; 75% of the estimates were obtained from samples exceeding 900 observations.

Results

Physician and patient participation in the medical access program

Panel (a) of Fig 2 plots the number of physicians across Canada who authorized medical cannabis use, by month, 2003–5 to 2014–3 (under the MMAR regime) and 2014–4 to 2021–12 (under the MMPR/ACMPR regime). Recall that under the MMAR, Health Canada adjudicated patient requests for medical cannabis. Under the MMPR and ACMPR regimes, Health Canada ceded prescribing authority to physicians. This policy change, and the attendant promulgation of provincial College regulations, evidently reduced the number of physicians participating in the medical access program. The policy change, however, no longer restricted medical cannabis to just severely ill patients; this may explain the increase in the number of patients registered in the program evident in panel (b) of Fig 2. At its peak, about 400,000 Canadians (just over 1% of the population) were registered. (An additional 40,000 individuals had licenses to cultivate cannabis under the ACMPR regime.) These two effects imply that the remaining participating physicians authorized cannabis use for a larger number of patients after the MMPR was introduced. Indeed, the number of patients per prescriber increased from about 5 under the MMAR regime to over 150 under the MMPR regime (panel c). It appears that this prescribing takes place mainly by physicians who work in “cannabis clinics” that specialize in cannabis authorizations, typically using online consultations [26]. In 2018, after the legalization of non-medical cannabis, the number of patients participating in the medical program declined.

Fig 2.

Fig 2

Number of physicians prescribing patient medical cannabis use (panel a), number of authorized patients, in thousands (panel b) and number of patients per physician (panel c), by month, 2003–5 to 2014–3 (MMAR) and 2014–4 to 2021–12 (MMPR/ACMPR). Note: Monthly data from the Marihuana Medical Access Regulations (MMAR) regime in blue. Data from the Marihuana for Medical Purposes Regulations (MMPR) and Access to Cannabis for Medical Purposes Regulations (ACMPR) regimes in red. The vertical line indicates the date of legalization of use of non-medical cannabis (October 2018). Data source: Health Canada administrative data provided to the authors.

Cannabis dosage size, dosage form, and potency

The average daily dose of dry cannabis authorized by Health Canada under the MMAR increased gradually from 5.6 grams/day in 2001 to 8.6 grams/day in 2011. Mean dosages then increased sharply to 12.1 grams/day in 2012 and 20.6 grams/day in 2013 [14]. It is unlikely that MMAR program enrollees consumed all the authorized cannabis dosage amounts. This is unlikely given the evidence from law enforcement personnel that cannabis grown under the auspices of the MMAR was being diverted [1].

Most authorized patients elected to use cannabis grown under a personal or delegated production license. In 2013, only 19% of the 36,797 authorized users procured cannabis directly from Health Canada [14]. There are no data on the THC and CBD concentrations of cannabis authorized under the MMAR. While Health Canada regulated the number of cannabis plants individuals could grow, potency was unregulated.

Under the MMPR/ACMPR, physician-authorized daily doses declined over time, from 4 grams of dry cannabis in mid 2014 to 2 grams in late 2020. The average daily amount per Licensed Producer shipment was markedly lower. For instance, in the fourth quarter of 2016, the mean physician authorized daily dose was 2.5 grams but the average daily amount per Licensed Producer shipment was 0.79 grams [18]. This reduction in cannabis doses likely reflects the expansion of the medical access program to include patients who experienced lower levels of morbidity compared to those who were eligible under the MMAR.

Panel (a) of Fig 3 reports the sales volumes, in kilograms, of both dry and oil cannabis, by month over the period April 2014 to September 2019. The data indicate that medical cannabis users were increasingly using cannabis oil instead of dry over this period. Cannabis oil sales grew steadily from their market introduction in early 2016, overtaking dry cannabis sales in early 2017, and grew until mid-2019. Unit sales declined in the final two months. Panel (b) of Fig 3 measures sales to consumers in “packaged units” of dry cannabis, cannabis extracts (previously labeled as oils) and edibles over the period October 2019 to March 2022. Medical cannabis users are increasingly using edibles (cannabis-infused drinks and foods). Measured in packaged units, unit sales of extracts, dry cannabis and edibles had roughly equal market shares by March 2022.

Fig 3. Volume of cannabis sales from Licensed Producers to registered patients, by cannabis presentation and month.

Fig 3

Panel (a) Volume in kilograms; dry and oil-based presentations; 2014–04 to 2019–09. Panel (b) Volume in packaged units; dry, extracts, and edible presentations; 2019–10 to 2022–03. Panel (a) data source: Health Canada administrative data provided to the authors. Note: after September 2018, cannabis oil sales volumes were measured in litres, not kilograms. Panel (b) data source: Health Canada administrative data obtained from Government of Canada Open Government website [20].

There are no statistics on the potency of the cannabis authorized by physicians under the MMPR/ACMPR, but this can be inferred from our survey of Licensed Producer product catalogs. We collected 18,703 observations on dry cannabis products and 6,939 observations on cannabis oil products collected monthly from June 2016 to December 2022. Fig 4 graphs the share of products on offer by Licensed Producers by concentration of THC and CBD and by presentation (cannabis oil, dried cannabis) and by month. Among the varieties of cannabis oil on offer, the product share of low THC—high CBD varieties is increasing and now account for the largest product share, slightly higher than the low CBD—high THC products. The latter group of products have been steadily declining over time. Among dry cannabis varieties, over 80% of products are high THC—low CBD and this share is increasing. The median THC content of the dry cannabis varieties available for sale in December 2022 is 20.5% and increasing over time. The median CBD content of the cannabis oil available for sale is about 13% and is also increasing.

Fig 4. Fraction of cannabis products sold by Licensed Producers, by THC and CBD concentrations, month (2016–06 to 2022–12) and presentation: Oil vs dry cannabis.

Fig 4

Data Source: monthly review of on-line Licensed Producers product catalogs.

Cannabis prices

Fig 5 reports the inflation-adjusted (i.e., “real”) pre-tax price trends of medical cannabis on offer from Licensed Producers by THC and CBD strength and by presentation. Panel (a) displays graphs for mean prices for dry cannabis; panel (b) displays graphs for cannabis oil. Real prices of dried cannabis have tended downwards during the last 3 years. The high THC, high CBD varieties are the exception; these prices have recently increased. The prices of most cannabis oil varieties have also declined in recent years. The exception are the prices for low THC, low CBD varieties.

Fig 5.

Fig 5

Mean real price of cannabis sold by Licensed Producers, by THC and CBD concentration, month (2016–06 to 2022–12) and presentation: dry (a) and oil (b). Data Source: monthly review of on-line product catalogs of Licensed Producers. Note: nominal prices deflated using all-item CPI with 2016–07 = 100. Prices do not include sales and excise taxes.

We next compare changes in Statistics Canada’s national medicinal cannabis real price index with changes in the prices of cannabis displayed above. The presentation and dosage strength specific real prices we collected dropped to varying degrees between January 2019 and October 2021: prices of high THC, low CBD dry varieties dropped by 21%. The low THC, high CBD oil prices dropped by 17% while the high THC, low CBD oil prices dropped by 42%. Statistic Canada’s price index declined by 32.4% over the same period, which is within the range of the price declines we found.

Province-level analysis of patient participation in the medical access program

We next focus on province-specific trends in patient participation in the medical access program. Table 1 presents data on the number of enrollees, number of enrollees with cannabis production licenses, and number of cannabis plants authorized under the MMAR, in December 2013, by province. Table 1 also displays the number of patients, production licenses and plants per 100,000 population aged 20 and older.

Table 1. Number of patients, number of patients with cannabis production licenses, and number of cannabis plants authorized under the MMAR, December 2013, by province.

Province # authorized patients # patients authorized to grow # plants allowed # auth patients per 100,000 pop 20+ # auth to grow per 100,000 pop 20+ # auth plants per 100,000 pop 20+ # plants per authorized grower
British Columbia 18,383 16,010 2,090,743 501 436 56,955 131
Alberta 2,364 1,328 151,446 79 44 5,048 114
Saskatchewan 952 423 20,249 116 52 2,469 48
Manitoba 855 735 82,059 91 78 8,735 112
Ontario 11,071 7,322 526,242 106 70 5,044 72
Quebec 1,120 891 78,826 18 14 1,233 88
New Brunswick 805 609 17,781 133 101 2,945 29
Nova Scotia 1,903 1,443 40,790 254 192 5,434 28
Prince Edward Island 78 - 741 70 - 661 -
Newfoundland 192 68 2,240 45 16 531 33

Data Source: # cannabis plants authorized: [1]; # patients authorized to grow: [14]; population estimates: [16].

Rates of cannabis use authorized under the MMAR program were particularly high in British Columbia. The number of enrollees per capita in that province were about double the rates in Nova Scotia, the next highest province. The number of authorized cannabis plants per capita in British Columbia was about 6 times the rate in Manitoba, the next highest province.

The MMPR regime, in effect from August 2013 to August 2016, banned personal and delegated cannabis production. Patients were required to obtain cannabis via mail order from Licensed Producers, until the ACMPR replaced the MMPR in 2016. Fig 6 displays the number of cannabis shipments from Licensed Producers per 1,000 population, by month, and patient province of residence. This graph covers the start of the MMPR regime in 2013 to March 2022.

Fig 6. Number of cannabis shipments from Licensed Producers per 1,000 population, by month, 2013–08 to 2022–03, and patient province of residence.

Fig 6

Note: The first red vertical line indicates the date of introduction of the Access to Cannabis for Medical Purposes Regulations (August 2016), which allowed those authorized to use medical cannabis to cultivate cannabis for personal use; the second red vertical line indicates the date of legalization of use of non-medical cannabis (October 2018). Data source: Health Canada administrative data provided to the authors.

The data indicate that medical cannabis consumption varied markedly across the provinces. Licensed Producer shipments per capita were particularly high in Alberta and Nova Scotia and particularly low in Quebec and British Columbia. The 2016 policy change that allowed for personal or delegated cultivation of medical cannabis did not appear to have an appreciable effect on rates of Licensed Producer shipments. Shipments dropped off in all provinces, to varying degrees, after the legalization of non-medical cannabis in late 2018. This suggests that some medical cannabis program enrollees elected to acquire cannabis outside of the medical access program, likely from the new retail channels allowed under the recreational cannabis program.

Impact of province-level factors on medical cannabis use under the MMPR and ACMPR

As was noted, the use of medical cannabis (as measured by shipments from Licensed Producers) varied considerably across provinces under the MMPR and ACMPR regimes. For instance, in January 2018, the per capita number of shipments in Alberta was over ten times the number in the neighbouring province of British Columbia. One potential reason for this variation was the willingness of physicians in the different provinces to authorize cannabis use. This willingness, in turn, could have been affected by the restrictions that the provincial Colleges imposed on cannabis prescribers. To investigate, we graphed province-specific medical cannabis use and the composite cannabis prescribing restriction score as of April 2016 (described in Table 2, below). Medical cannabis use was measured using the average monthly shipments from Licensed Producers per 100,000 population, March to May 2016.

Table 2. Provincial College of Physicians restrictions on prescribing of medical cannabis, by province, April 2016.

province
prescribing physician must … bc ab sk mb on pq nb ns pe nf
meet with patient every 3 months 3 3
register with regulator as cannabis prescriber 2
review patient’s medicines use 2 2
send in Medical Document to LP 1
be patient’s primary physician 3 3
meet patient in person to prescribe 1 1 1
have patient sign written treatment agreement 1 1 1
have patient enroll in research study 2
create and maintain registry of patients using cannabis 4
have patient sign consent form 1 1 1
assess patient risk of addiction using standardized tool 1.5 1.5 1.5 1.5
implement process to identify patient misuse 2 2 2 2 2 2
keep medical documents separate for inspection by regulator 1 1 1 1
specify THC percentage on Medical Document 0.5
specify medical condition on Medical Document 0.5 0.5 0.5
composite cannabis prescribing restriction score 7.5 11 5.5 6.5 5 13 0 1 4 4.5
Higher scores indicate more restrictions

Data Source:

British Columbia: College of Physicians and Surgeons of British Columbia–Practice Standard: Cannabis for Medical Purposes: https://www.cpsbc.ca/files/pdf/PSG-Cannabis-for-Medical-Purposes.pdf

Alberta: College of Physicians and Surgeons of Alberta (BPSA)–Cannabis for Medical Purposes Standard of Practice: https://cpsa.ca/physicians/standards-of-practice/cannabis-for-medical-purposes/

Saskatchewan: College of Physicians and Surgeons of Saskatchewan–Medical Cannabis: https://www.cps.sk.ca/imis/CPSS/CPSS/Programs_and_Services/Medical_Marijuana/Medical_Cannabis.aspx

Manitoba: College of Physicians and Surgeons of Manitoba–Standard of Practice Authorizing Cannabis for Medical Purposes: http://www.cpsm.mb.ca/assets/Standards%20of%20Practice/Standard%20of%20Practice%20 Authorizing%20Cannabis%20for%20Medical%20Purposes.pdf

Ontario: College of Physicians and Surgeons of Ontario–Cannabis for Medical Purposes: https://www.cpso.on.ca/Physicians/Policies-Guidance/Policies/Cannabis-for-Medical-Purposes

Quebec: College des Medecins du Quebec–Ordonnance de Cannabis a des Fins Medicales: http://www.cmq.org/publications-pdf/p-1-2018-09-20-fr-ordonnance-cannabis-fins-medicales.pdf

New Brunswick: College of Physicians and Surgeons of New Brunswick–Guidelines: Medical Marijuana: https://cpsnb.org/en/medical-act-regulations-and-guidelines/guidelines/444-medical-marijuana

Nova Scotia: College of Physicians and Surgeons of Nova Scotia–Professional Standards Regarding the Authorization of Marijuana for Medical Purposes: https://cpsns.ns.ca/wp-content/uploads/2017/12/Authorization-of-Marijuana-Medical-Purposes.pdf

Prince Edward Island: The College of Physicians and Surgeons of Prince Edward Island–Prescribing of Medical Marijuana Policy: https://cpspei.ca/wp-content/uploads/2017/03/Marijuana-Prescribing-Nov-3016.pdf

Newfoundland and Labrador: College of Physicians and Surgeons of Newfoundland and Labrador–Medical Marihuana: Advisory and Interim Guideline: https://imis.cpsnl.ca/WEB/CPSNL/Policies/Advisory_and_Interim_Guideline_-_Medical_Marihuana.aspx

The scatterplot (Fig 7) reveals that per capita medical cannabis shipment volume tended to be lower in provinces with stricter College restrictions on cannabis prescribing.

Fig 7. Average monthly cannabis shipments from Licensed Producers per 100,000 population, March to May 2016, and composite cannabis prescribing restriction score, by province.

Fig 7

Note: BC = British Columbia, AB = Alberta, SK = Saskatchewan, MB = Manitoba, ON = Ontario, QC = Quebec, NB = New Brunswick, NS = Nova Scotia, PE = Prince Edward Island, NF = Newfoundland and Labrador. Shipments Data Source: Health Canada administrative data provided to the authors.

One possible reason for this association is that rates of regular cannabis use–both medical and non-medical–are lower in provinces with stricter College regulations. However, Fig 8 reveals that the estimated fraction of regular users who are enrolled in the medical access program also tended to be higher in provinces with less stringent prescribing controls. Thus, it appears that the cannabis prescribing restrictions affected rates of participation in the medical cannabis program.

Fig 8. Ratio of patients enrolled in medical cannabis access program to the estimated population aged 20 years and older that uses cannabis daily or weekly, by province, July 2015.

Fig 8

Data Source: Enrollment in medical access program (MAP): Health Canada administrative data provided to the authors. Estimated population aged 20 years and older that uses cannabis daily or weekly: 2015 Statistics Canada Canadian Tobacco, Alcohol and Drugs Survey. BC = British Columbia, AB = Alberta, SK = Saskatchewan, MB = Manitoba, ON = Ontario, QC = Quebec, NB = New Brunswick, NS = Nova Scotia, PE = Prince Edward Island, NL = Newfoundland and Labrador.

Fig 7 also suggests that some variation in the volume of Licensed Producer shipments was due to factors other than prescribing restrictions. In particular, British Columbia and Manitoba had particularly low shipment volumes, and Alberta, high volumes, given their prescribing restriction score. The low volume of Licensed Producer shipments to British Columbia and Manitoba could have been due to medical cannabis users in these provinces accessing cannabis from plants that were established under production licenses in the previous MMAR regime.

Rates of regular cannabis use in the community over time

As Table 1 illustrates, during the MMAR regime, almost 3 million cannabis plants were licensed for cultivation in residences. Fig 2 illustrates a marked increase in the number of enrollees in the medical cannabis program across most provinces after eligibility requirements were relaxed in 2013. There was a concurrent increase in medical cannabis sales volumes, from about 300 kg/month in early 2015 to over 6000 kg/month in mid 2018 (Fig 3). This liberalization of the medical cannabis access program may have increased awareness of cannabis’ therapeutic uses and reduced the social stigma from its use. Home-based cultivation, followed by the creation of the Licensed Producer industry may have also increased the availability of cannabis through unauthorized channels, such as through dispensaries and online dealers.

To investigate, we examined rates of regular (daily or almost daily) cannabis use among each provincial adult population from 1989 to 2021; this period spans the different medical cannabis access program regimes and the 2018 legalization of recreational cannabis. These estimates were obtained from the various national health and drug use surveys conducted over this period; we used the sampling weights provided in each survey to render the estimates representative of the residential adult population.

The following features are evident from the province-specific graphs displayed in Fig 9. First, rates of regular cannabis use increased in all provinces over the three decades. Second, the introduction of the 2003 MMAR did not appear to result in an increase in regular cannabis use. However, the 2014 MMPR regime appeared to increase rates of regular use in all provinces, except for Quebec. Finally, the legalization of recreational cannabis in 2018 appeared to markedly increase daily cannabis use in some provinces.

Fig 9. Estimated fraction of community dwelling population aged 20 years and older that consumes cannabis daily or almost daily, by province, survey, and year, 1989–2021.

Fig 9

Note: the blue line is a median spline curve fitted to the provincial estimates (the blue dots). The red vertical lines indicate the introduction of the following policies: 1) the 2001 Marihuana Medical Access Regulations (MMAR) regime which provided medical cannabis access to severely ill patients; 2) the 2014 Marihuana for Medical Purposes Regulations (MMPR) regime which delegated medical cannabis authorization to physicians and expanded the indications for cannabis use; and 3) the 2018 legalization of recreational cannabis. Data source: 1989 National Alcohol and Drugs Survey; 1994 Canada’s Alcohol and Other Drugs Survey; 2002 Canadian Community Health Survey; 2004 Canada Addiction Survey (CAS); 2005–2013 Canadian Tobacco Use Monitoring Survey; 2008–2012 Canadian Alcohol and Drug Use Monitoring Surveys (CADUMS); 2013, 2015, 2017 Canadian Tobacco, Alcohol and Drugs Survey; 2019–2021 Canadian Tobacco and Nicotine Survey; and the 2018, 2019 and 2020 National Cannabis Survey (NCS). All surveys were conducted by Statistics Canada except for the 2004 CAS, the 2008–2012 CADUMS, and the 2018–2020 NCS which were commissioned by Health Canada and conducted by private sector survey firms.

Rates of regular cannabis use in the community and participation in the medical access program over time

Finally, we compared the national participation rates in the medical access program from 2005 to 2021 to the estimated rates of daily cannabis use over the same period (Fig 10). The difference between these reflects the estimated fraction of the adult population that uses cannabis daily outside of the medical cannabis access program and thus likely without physician supervision. We find that only a small fraction of regular users enrolled in the medical access program during the MMAR regime. Rates of enrollment in the medical access program increased under the MMPR, but rates of daily cannabis use increased even faster. Thus, the fraction of daily users who did so outside of the medical access program increased under the MMPR regime. This fraction increased again after the legalization of recreational cannabis use in 2018.

Fig 10. Estimated fraction of national community dwelling population aged 20 years and older that consumes cannabis daily or almost daily, by month, and estimated fraction of population age 20 years and older enrolled in medical cannabis access program, by month 2005m1 – 2021m12.

Fig 10

Note: the blue line is a median spline curve fitted to the national estimates of fraction of population 20+ that uses cannabis daily (the blue dots). The red line is a median spline curve fitted to the national participation rates in the medical access program (the red dots). The green vertical lines indicate the introduction of the following policies: 1) the 2014 Marihuana for Medical Purposes Regulations (MMPR) regime which delegated medical cannabis authorization to physicians and expanded the indications for cannabis use; and 2) the October 2018 legalization of recreational cannabis.

Discussion

This study is the first to examine long-term trends in Canada’s medical cannabis sector and to relate these trends to the medical and recreational cannabis regulatory policy changes. Health Canada initially restricted access to those who had the personal approval of the federal Minister of Health. The courts ruled that the approvals process infringed patients’ constitutional rights [2]. Health Canada, in turn, launched a medical cannabis access program in 2001 that granted access to those with physician-documented evidence of a severe health problem that could not be managed using conventional therapies. Most patients accessed cannabis grown under a personal or delegated production license. By 2013, almost 3 million plants were authorized and the average authorized daily consumption was about 18 grams. Concerned over production safety and illegal diversion, Health Canada in 2014 required that cannabis be purchased from a Licensed Producer, a regulated commercial grower; personal production was banned. Health Canada also ceded to physicians responsibility for authorizing patient access to cannabis.

To fill the regulatory void, each of the physician Colleges imposed their own prescribing restrictions. The number of physicians who were willing to support patient cannabis use subsequently fell; the physicians that were willing to do so, however, authorized cannabis use for large numbers of patients. The result was a marked increase in the number of patients participating in the program.

The post-2014 increase in medical cannabis use varied by province–rates of medical cannabis use and the fraction of regular cannabis users who participated in the medical cannabis program were generally lower in provinces with stricter regulations on physician cannabis prescribing. This finding is consistent with survey results reported by Belle-Isle and colleagues; patients in some provinces reported difficulty in finding physicians willing to support medical cannabis use and thus turned to dispensaries and other unsanctioned outlets [27]. It also seems plausible that the low rate of program participation in British Columbia was due to the availability of cannabis from dispensaries. In less populous regions of the province, in which the federal police force, the Royal Canadian Mounted Police (RCMP), provided local law enforcement, illicit cannabis distribution was forced to go underground. However, law enforcement agencies in some large cities in the province allowed cannabis dispensaries to operate [28]. The City of Vancouver even regulated cannabis dispensaries, despite their illegality at the time [29]. Province-wide, the average penalty issued for cannabis possession in BC was lower than in other provinces [30]. This suggests that some of the interprovincial variation in the participation in the MMPR regime was due to variation in the propensity of authorities to enforce the CDSA.

It appears that patients who participate in the medical access program increasingly are using cannabis oils instead of dried cannabis. This accords with the results of surveys of individuals who report using cannabis for medical reasons [3133]. Most varieties of cannabis oil sold by Licensed Producers are now high in CBD and low in THC. Dry cannabis varieties, conversely, tend to be high in THC and low in CBD.

A key policy question is the price spread between medical cannabis grown by Licensed Producers and cannabis available from unauthorized sources. Medical cannabis is typically more expensive because it is subject to excise and sales taxes and must meet stringent production safety requirements. Ideally, the price difference between authorized and unauthorized cannabis is sufficiently small such that consumers would select the former source. We find that real prices of most varieties of medical cannabis are declining over time. However, there is little information on changes in the illicit market prices for the same varieties favored by medical cannabis users; the available evidence focuses on prices of dry cannabis [34, 35].

We estimated rates of daily cannabis use (medical use or otherwise) by province using national surveys conducted over the last three decades and find that rates increased markedly after the introduction of the 2014 MMPR policy regime. Only a small fraction of daily cannabis users (<10%) were enrolled in the medical cannabis access program. The fraction of Canadians using cannabis daily increased markedly after the 2018 legalization of recreational cannabis; at the same time, participation in the medical access program declined. This suggests that increasing numbers of Canadians are using cannabis daily without medical supervision. The literature indicates that individuals who use cannabis therapeutically use it primarily to manage pain and insomnia, and to alleviate the symptoms of psychiatric disorders (such as anxiety and depression) [33, 36, 37]. The health outcomes of the growing numbers of patients using cannabis regularly–and evidently without physician supervision–remains an important area for future research.

Acknowledgments

We thank two anonymous referees for helpful comments and thank Jonathan Fortin at Health Canada for supplying administrative data. We acknowledge the research assistance of Igor Korolija.

Data Availability

The data are available at: Grootendorst, Paul, 2023, "Replication Data for: Canada medical cannabis access regime administrative data and licensed producer catalog data", https://doi.org/10.5683/SP3/SXSYPD, Borealis

Funding Statement

The author(s) received no specific funding for this work.

References

Decision Letter 0

Julian Aherne

10 Oct 2022

PONE-D-22-17767Lessons from 20 years of medical cannabis use in CanadaPLOS ONE

Dear Dr. Grootendorst,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

We urge you to pay particular attention to the concerns of reviewer 2 regarding the data handling, transparency, and accessibility. Further, reviewer 1 notes that the manuscript needs to be revised to be more accessible to a non-Canadian (international) audience. Overall, both reviewers raise a number of substantive concerns.

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I have received comments from two reviewers, they waiver between major revisions and reject but note that it is a “potentially interesting and useful paper”. I have recommended major revisions under the assumption that a revised manuscript can adequately address all reviewers’ concerns. I urge the authors to pay particular attention to the concerns of reviewer 2 regarding the data handling, transparency, and accessibility. Further, reviewer 1 notes that the manuscript needs to be revised to be more accessible to a non-Canadian (international) audience. Please provide a point-by-point response to each reviewers comment and indicate how the manuscript has been revised.

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Reviewer #1: Partly

Reviewer #2: Yes

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Reviewer #1: Yes

Reviewer #2: N/A

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Reviewer #2: No

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Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: This is a potentially interesting and useful paper on the evolution of Canada’s medical cannabis system during the past two decades. The paper points to an interesting story about the interplay of changes in policy at the federal and provincial levels and how those change were reflected in amount of cannabis produced and consumed, the nature of cannabis products, and price of cannabis. The paper would be improved by some edits to help make the paper more accessible to a non-Canadian audience and more clearly describing variation and changes provincial policies. Below are specific suggestions.

1. Not being Canadian, I was unsure what Health Canada and physician Colleges are. The authors should make edits in the Abstract and throughout the paper to make the paper more accessible to a non-Canadian audience. I believe that physician Colleges set province-specific guidelines for medical cannabis, but that is not clearly stated anywhere in the paper.

2. The interplay between provincial and federal regulations could perhaps be discussed more clearly. Pre-2014, it seems there was a huge difference across provinces in authorizations for medical cannabis (lots more medical cannabis authorized in BC), but this changed in 2014 when a system of commercial growers was created. After 2014, it looks like the size of the medical cannabis market was relatively small in BC. I don’t think this dramatic shift is clearly explained in the paper. Maybe there is no easy explanation. There is a story here about variation in policies, regulations, and maybe enforcement of regulations across provinces and how those things evolved across years.

3. The section spanning pages 4 through 6 could be more succinct and would perhaps be helped by a figure showing a policy-change timeline. Ideally, you might have separate timelines for each province as well, although I am not sure that information on changes in province-level policies across years is available to the authors. (They do have information on provincial variation in restrictions in 2016.)

4. The issue of variation in enforcement of cannabis laws might be worth addressing more explicitly. In the US, one aspect of liberalization of cannabis policy is decriminalization, involving reduced priority given to enforcement of cannabis laws as well as reduction in penalties for violation of cannabis laws. I was unable to figure out how much of this is an issue in Canada’s cannabis laws. One guess I have about what happened in BC is that after cannabis growing by those authorized for medical cannabis was banned, very little effort was put into enforcing that ban and people continued to supply themselves by growing their own cannabis (or having a friend who grew their own) rather than switching to authorized commercial growers. There was probably a lot of diversion occurring in BC, although from Figure 8 it does not look like population-wide prevalence of daily or near daily use was much higher in BC than most other provinces.

5. There were some numbers that were surprising to me about the average number of grams per day per medical cannabis user. In dry form, a gram of cannabis is about 3 joints. Someone who uses daily and heavily might use 1 to 2 grams per day. I was surprised to see 18 grams per day allowed under MNAR in 2013 (page 5) or the average daily dose of cannabis authorized by Health Canada of 5.6 grams (page 10). Even 2 grams per day prescribed by physicians under MMPR (page 11) seems awfully high. Am I misunderstanding something?

6. The authors put information on variation in medical cannabis restrictions by province in 2016 in an online supplement. I would like to see this table included in the body of the paper.

7. In examining national survey data on cannabis use, the authors focus on daily or near daily use. What was the cutoff for daily use? A common cutoff is 20+ days of use in the past 30. Is that what was used here?

8. The authors provide information on price and potency separately for dry cannabis and oils. The authors should briefly clarify how these are linked to different routes of administration (e.g., smoking, vaping, dabbing, and edibles).

9. Does Figure 4 correct for inflation?

Reviewer #2: Uploaded letter, attached.

The authors provide an extensive descriptive history of the Canadian medical cannabis regime by collating data from a wide variety of sources to provide an integrated overview of how the sector has evolved since inception. An extensive amount of data is processed to provide statistical snapshots of several dimensions of the Canadian medical cannabis system over time, including after legalization. The analysis I believe is mostly novel, the manuscript is well-written if not always technically clear, and there are no statistical errors that I can identify.

Unfortunately I can only recommend that PLOS reject the manuscript. The data handling, transparency, and accessibility clearly do not meet the standards of PLOS. This could be potentially fixed, which makes a case for major revisions, but my reading of the manuscript and the authors’ declarations suggests they will be unable to meet the PLOS data standards and hence I recommend rejection. I lay out a number of crucial issues leading to this recommendation below.

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Decision Letter 1

Julian Aherne

7 Feb 2023

PONE-D-22-17767R1Lessons from 20 years of medical cannabis use in CanadaPLOS ONE

Dear Dr. Grootendorst,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

Please ensure that the revised manuscript, including the abstract, is accessible to an international audience; provide clarification regarding the number of grams authorized; and give the manuscript a thorough edit to increase clarity, e.g., ensure manuscript is written entirely in the past tense.

Please submit your revised manuscript by Mar 24 2023 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

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If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: https://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols.

We look forward to receiving your revised manuscript.

Kind regards,

Julian Aherne

Academic Editor

PLOS ONE

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Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

Additional Editor Comments:

Based on the comments from one reviewer, the manuscript requires minor revisions: please ensure that the paper, including the abstract, is accessible to an international audience; provide clarification regarding the number of grams authorized; and

lastly the manuscript requires a thorough edit to increase clarity, e.g., ensure manuscript is written entirely in the past tense. I look forward to your revised submission.

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Reviewer #1: (No Response)

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2. Is the manuscript technically sound, and do the data support the conclusions?

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Reviewer #1: Partly

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

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6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: The revised manuscript includes additional information requested by the other reviewer and me. The authors’ responses to our question and suggestions were thoughtful. I continue to think the information on the evolution of medical cannabis is Canada presented in the manuscript will be useful to the field. The authors do not run statistical models assessing statistical significance of associations or estimating magnitude of “effects” of policy changes. I think that is fine, although there are place in the paper where the authors should make edits to be more cautious about causal inferences.

The other reviewer raised concerns about data sharing and transparency. My understanding is that almost all the data used by the authors is already publicly available. Where they have put effort into interpreting or coding that data—e.g., rating restrictiveness of province policies—they provide information on their process for doing so. I am not entirely clear on all the rules for data sharing in PLOS ONE publications, but it seems like the authors are in accord with the spirit of transparency.

I had requested the authors make sure their paper was accessible to an international audience. The authors added some clarification on how the system of physician Colleges works in setting province-specific policies into the main body of the paper. It would help readers if the Abstract was written in a way that made it clear what Health Canada and physician Colleges are.

Both the other reviewer and I reacted to information reported on average daily doses of cannabis. The response letter provided some reasons why the average authorized dose under MMAR would have been so high. My takeaway from the authors response is that the number of grams authorized under MMAR, the average number of grams supplied under MMPR, and the actual number of grams per day consumed by medical cannabis users are very different things. It would help the reader if the authors added some clarifying information to the text of the manuscript. If they don’t, many readers, thinking in terms of actual grams consumed, are going to think that the high numbers are due to typographical or data coding errors.

In general, the writing quality of the paper is fine in terms of clarity. That said, this paper presents a lot of information and, if you are not Canadian, a lot of that information is new and confusing. The content of the paper also does not neatly fit into the conventional format of journal article. For example, should history of medical cannabis policy be in the Results section of the Abstract? The structure of the Abstract and the body of the manuscript do not match. The paper could be published in close to its current form, but I believe the authors would be much happier with their paper, and it would receive a much wider audience, if it received a thorough edit to increase clarity, eliminate some typographical and grammatical errors, increase precision of word choice, and, in general, make the paper more reader friendly. One recommendation I have is that the paper be written almost entirely in the past tense. There are several places where the authors slip into the present tense, which tends to impart stronger inferences than the past tense. The strength of inferences is general issue with this paper. The manuscript is primarily descriptive. I would caution against make statement that imply specific policy changes “caused…”

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PLoS One. 2023 Mar 23;18(3):e0271079. doi: 10.1371/journal.pone.0271079.r004

Author response to Decision Letter 1


8 Mar 2023

In this revision,

• we have revised the abstract as requested.

• we now clarify that MMAR program enrollees likely did not consume all the authorized cannabis dosage amounts (especially given the concerns that cannabis was being diverted).

• we removed any statements that implied that a specific policy change exerted a causal impact on the outcome variables studied in this paper.

• we have also thoroughly edited the manuscript to improve clarity.

Attachment

Submitted filename: response to reviewers r2.docx

Decision Letter 2

Julian Aherne

9 Mar 2023

Lessons from 20 years of medical cannabis use in Canada

PONE-D-22-17767R2

Dear Dr. Grootendorst,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

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PLOS ONE

Additional Editor Comments (optional):

The revised manuscript addresses the concerns of the reviewers. I recommend that it is accepted for publication.

Reviewers' comments:

Acceptance letter

Julian Aherne

15 Mar 2023

PONE-D-22-17767R2

Lessons from 20 years of medical cannabis use in Canada

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    Submitted filename: response to reviewers r2.docx

    Data Availability Statement

    The data are available at: Grootendorst, Paul, 2023, "Replication Data for: Canada medical cannabis access regime administrative data and licensed producer catalog data", https://doi.org/10.5683/SP3/SXSYPD, Borealis


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