Cannabis sativa (L), a plant with an extensive history of medicinal usage across numerous cultures, has received increased
attention over recent years for its therapeutic potential for gynecological disorders such as endometriosis, chronic pelvic
pain, and primary dysmenorrhea, due at least in part to shortcomings with current management options. Despite this grow -
ing interest, cannabis inhabits an unusual position in the modern medical pharmacopoeia, being a legal medicine, legal
recreational drug, and an illicit drug, depending on jurisdiction. To date, the majority of studies investigating cannabis use
have found that most people are using illicit cannabis, with numerous obstacles to medical cannabis adoption having been
identified, including outdated drug-driving laws, workplace drug testing policies, the cost of quality-assured medical can-
nabis products, a lack of cannabis education for healthcare professionals, and significant and persistent stigma. Although
currently lacking robust clinical trial data, a growing evidence base of retrospective data, cohort studies, and surveys does
support potential use in gynecological pain conditions, with most evidence focusing on endometriosis. Cannabis consumers
report substantial reductions in pelvic pain, as well as common comorbid symptoms such as gastrointestinal disturbances,
mood disorders such as anxiety and depression, and poor sleep. Substitution effects were reported, with >50% reduction or
cessation in opioid and/or non-opioid analgesics being the most common. However, a substantial minority report not disclos-
ing cannabis consumption to their health professional. Therefore, while such deprescribing trends are potentially beneficial,
the importance of medical supervision during this process is paramount given the possibility for withdrawal symptoms.
Plain Language Summary
Cannabis, whether purchased illicitly, or obtained through legal means, is commonly used by those with chronic pelvic pain,
especially people with endometriosis. People report several benefits from using cannabis, including being able to reduce
their normal medications including opioid based painkillers, but often don’t tell their health professional about this. This
could lead to issues with withdrawal symptoms, so clinicians should be aware of the high prevalence of use of cannabis in
this population.
* Justin Sinclair
[email protected]
* Mike Armour
[email protected]
1 NICM Health Research Institute, Western Sydney
University, Sydney, NSW, Australia
2 Division of Obstetrics and Gynaecology, School of Clinical
Medicine, Medicine and Health, UNSW, Sydney, NSW,
Australia
3 Gynaecological Research and Clinical Research (GRACE)
Unit, Royal Hospital for Women, UNSW, Sydney, NSW,
Australia
4 Translational Health Research Institute, Western Sydney
University, Sydney, NSW, Australia
5 Medical Research Institute of New Zealand (MRINZ),
Wellington, New Zealand
Key Points
Robust clinical trial data is currently lacking for gyneco-
logical pain conditions.
Despite this, cannabis is being used to treat gynecologi-
cal pain, especially in those with endometriosis or other
forms of chronic pelvic pain, with reductions in symp-
toms such as pelvic pain commonly reported.
Cannabis consumption for gynecological pain should be
undertaken under medical supervision, especially when
reducing pharmaceutical interventions like opioids.
1572 J. Sinclair et al.
1 Introduction
Current global estimates suggest 39.6% of women and those
assigned female at birth* (hereafter denoted as women)—or
approximately 1.53 billion people, live with gynecological
disease [1], with pain often a key symptom. The most com-
mon causes of gynecological pain are primary or secondary
dysmenorrhea, with over 70% of women reporting dysmen-
orrhea (period pain) at some stage of their life [2 ]. Primary
dysmenorrhea is defined as menstrual pain in the absence of
underlying structural changes [3]. Primary dysmenorrhea’s
characteristic symptom is crampy, colicky spasms of pain in
the suprapubic area, occurring within 8–72 h of menstrua-
tion and peaking within the first few days as menstrual flow
increases [3, 4]. In addition to painful cramps, many women
with primary dysmenorrhea experience other menstrual-
related symptoms, including back and thigh pain, headaches,
diarrhea, nausea, and vomiting [4]. The largest contributing
physiological factor in primary dysmenorrhea is increased
amounts of prostaglandins present in the menstrual fluid [5].
If there is no pregnancy after ovulation, progesterone levels
decline in the late luteal phase of the cycle. Reduction in
progesterone levels destabilizes cell membranes in endo-
metrial tissue and causes the hydrolyzation of cell mem-
brane phospholipids (mainly omega-6) to form arachadonic
acid. Arachadonic acid is converted via the cyclooxygenase
pathway to prostaglandins PGE2 and PGF2a [5 , 6]. These
excess prostaglandins are released when the endometrial lin-
ing breaks down during menses. Prostaglandins, especially
PGF2a, stimulate myometrial contractions, reducing uterine
blood flow and causing uterine hypoxia. This is responsible
for the painful cramping that characterizes primary dysmen-
orrhea [5 , 7]. Secondary dysmenorrhea is menstrual pain
associated with structural changes in the pelvis or an identifi-
able cause such as endometriosis [4]. In Australia and other
high-income countries, persistent dysmenorrhea is reported
in over 90% of women and girls under age 25 years [8 , 9].
Dysmenorrhea may lead to absenteeism at work [10], and
affect attendance and academic performance both at school
and in tertiary education [2 ], with many people reporting
inadequate symptom management [11–13].
Chronic pelvic pain (CPP), defined as pain in the pel-
vis for > 6 months’ duration that is severe enough to cause
functional disability or require medical intervention [14] is
a common type of gynecological pain [15– 17]. CPP may
be cyclic, non-cyclic or both [ 18] and commonly includes
dysmenorrhea (period pain), non-cyclical pelvic pain, dys-
pareunia (painful intercourse), dysuria (pain on urination),
and dyschezia (pain on defecation) [19]. CPP affects one in
four women (26%) [18, 20], accounting for 40% of laparos-
copies, 10% of specialist gynecology consultations, and 12%
of hysterectomies in the USA annually [18]. CPP includes
conditions such as endometriosis, adenomyosis, vulvodynia,
interstitial cystitis, and bladder pain syndrome [19, 21, 22],
with endometriosis the single most prevalent disease in this
group [23]. Symptom management is frequently challenging
due to involvement of neuropathic, nociplastic, and nocicep-
tive pain pathways [21].
Current management strategies for gynecological pain
depend on its underlying cause. Primary dysmenorrhea is
commonly managed by non-steroidal anti-inflammatory
drugs (NSAIDs) and/or the oral contraceptive pill as first-
line treatment(s) [24], however a significant number of
women report less than optimal symptom management,
with 25% of those using ibuprofen and 35% of those using
paracetamol reporting no reduction in dysmenorrhea sever-
ity [12]. This may explain why women are open to using
other treatments such as cannabis to manage their primary
dysmenorrhea symptoms [13]. Current treatments for endo-
metriosis and chronic pelvic pain are generally considered
suboptimal by those with the disease [15, 25], with only
25% of those with endometriosis being satisfied with their
symptom management [25]. There are concerns about lack
of effectiveness and problematic side effects of many medi-
cations for pelvic pain, leading to discontinuation rates of
25–50% [26]. Opioid analgesics are not recommended for
chronic pelvic pain due to both a lack of efficacy and safety
concerns with respect to ongoing use [27]. However, despite
this they continue to be prescribed; women with endometrio-
sis have a four times greater risk of chronic opioid use com-
pared with women with no endometriosis [28]. For those
with endometriosis, surgery is considered the gold standard
but often has significant costs, long waiting times [29], and
substantial recurrence rates, even with expert endometriosis
surgeons [30].
Given the prevalence of gynecological pain, its delete-
rious effect on quality of life, and the current difficulties
in managing this pain, finding effective, safe interventions
with low addictive/dependence potential is identified as an
international priority [31– 33].
2 Historical Use of Cannabis
Cannabis sativa is one of the oldest cultivated plants utilized
by humans, being used as a food, textile and as a medicine
for millennia [34–36]. The Ebers Papyrus (1550 BCE) from
ancient Egypt describes the use of cannabis to aid child -
birth [37]. In ancient China, the use of cannabis for female
reproductive symptoms was reported in the Pen-Tsao Ching,
based on the oral traditions passed down from the Emperor
Shen-Nung, who lived circa 2700 BCE [36, 38]. The age-
old Indian Atharva Veda of 1000 BCE described cannabis
as a sacred plant, used as an analgesic, anesthetic, anti-
inflammatory, anti-spasmodic, and hypnotic medicine [36].
1573
Cannabis for Gynecological Conditions
More recently, the Chinese Bencao Gang Mu compiled in
1596 recommended cannabis flowers for menstrual disorders
[37], the Persians utilized it for calming uterine pains [37],
African cultures utilized it to facilitate childbirth, and South
American cultures reported its utility for menstrual cramps
in the 16th century [36].
Cannabis was introduced to Western medicine in 1842
by the Irish physician O’Shaughnessy [37]. Soon after, it
was acknowledged in the Dispensatory of the United States,
and tinctures of cannabis were prescribed to manage uter -
ine hemorrhage [39], assistance in childbirth [40], neuralgic
dysmenorrhea [41], hyperemesis gravidarum, dysmenorrhea,
and heavy menstrual bleeding—the latter being published
in the British Medical Journal [ 37, 42]. In the 19th cen-
tury, cannabis was also prescribed as an anodyne in chronic
metritis, endometritis, and chronic cystitis [37]. Importantly,
cannabis was found to have advantages over opiates for
pain [43], and could also be useful for opiate withdrawal
[44–46]. Notwithstanding its widespread popularity, can-
nabis started falling out of favor as a medical treatment in the
early 20th century, due mainly to a lack of quality assurance
and standardization from imported material [47]—factors
that were being addressed by the newly birthed pharmaceu-
tical industry and its single active drug model. However,
with the implementation of the Marihuana Tax Act in 1937
[48], which effectively criminalized the possession and use
of cannabis as a medicine in the US, widespread medical
use largely ceased. Cannabis was subsequently removed
from the United States Pharmacopoeia in 1942 and was
added to the United Nation’s Single Convention on Narcotic
Drugs in 1961. Cannabis was prohibited through the US
Controlled Substances Act of 1970 where it was classified
as a Schedule 1 controlled substance—defined as having
no accepted medicinal use, high abuse potential, and con-
cerns for dependence [48]. Whilst history suggests that the
drivers for this prohibitionist position were more idealistic
than evidence-based [49, 50], the fact remains that Cannabis
sativa remains a largely prohibited substance globally, with
changes to legislation only relatively recently allowing for
medicinal use in a growing number of nations.
Despite decades of prohibition and Schedule 1 relegation,
research into the therapeutic potential of cannabis continued
largely unabated, with two of the main active constituents
of cannabis, the terpeno-phenolic cannabinoids cannabidiol
(CBD) and delta-9-tetrahydrocannabinol (THC) discovered
in 1940 and 1964, respectively [51, 52]. Cannabidiol, a non-
intoxicating cannabinoid, has a wide range of pharmaco -
logical activities, including neuroprotective, anti-convulsant,
anxiolytic, analgesic, anti-depressant, antioxidant, and anti-
inflammatory properties [53– 58]. THC also has a broad
array of pharmacological actions, including analgesic, anti-
emetic, anti-inflammatory, muscle relaxant, and sedative
properties [59–62]—all of which can be of potential benefit
to gynecological pain conditions, but must be balanced with
its intoxicating effects. To date, there are over 144 different
cannabinoids identified across the Cannabis genus [63], with
research ongoing into their pharmacological activities and
potential benefit in human health. Additional research has
also identified an entire neuromodulatory system within the
body—the endocannabinoid system (ECS)—with receptors
identified in most organ systems, including the female repro-
ductive system, resulting in various changes to physiological
processes [64].
3 Mechanisms of Action
The ECS consists of G-protein coupled receptors (i.e., Can-
nabinoid 1 and 2 receptors), endogenous ligands (i.e., the
endocannabinoids), and ligand metabolic enzymes [65]
responsible for the synthesis and degradation of endocan-
nabinoids. More broadly, the ECS is involved in the mod-
ulation of a host of physiological responses, inclusive of
inflammation, nociception, appetite regulation, respiration,
and metabolism [66], with more recent research highlighting
ECS involvement across many aspects of the female repro-
ductive system. The ECS engages in a complex interplay
with the hypothalamic pituitary ovarian (HPO) axis to exert
control over certain female reproductive processes [67],
including pain modulation, oocyte maturation, ovarian endo-
crine secretion, folliculogenesis, uterine decidualization and
placentation, implantation, and embryo transport [67– 69].
Research into the role of ECS in gynecological conditions
has highlighted that elevated systemic levels of endocan-
nabinoids (i.e., anandamide and 2-arachidonoyl glycerol
[2-AG]), along with decreased local cannabinoid 1 receptor
(CB1) expression are present in people with endometriosis
[70], and that the ECS may be a promising target to address
endometriosis-related pain [71–73]. Furthermore, alterations
in ECS homeostasis may lead to dysfunctional modulation
of cellular processes involved in reproductive pathologies,
namely pre-eclampsia, miscarriage, and ectopic pregnancy
[74]. Research also posits that ECS dysfunction is involved
in the pathogenesis of dysmenorrhea in adenomyosis [75].
Proposed mechanisms by which both endocannabinoids
and cannabinoids exert analgesic effect across gynecologi-
cal pain and associated disorders are numerous and inter-
related. Neural and non-neural cells produce arachidonic
acid derivatives known as endocannabinoids in response to
tissue injury [76]. These endocannabinoids, mainly anan-
damide and 2-AG, modulate neural pain signal conduction
by mitigating sensitization and inflammation via activation
of cannabinoid receptors, which are also targets for phyto-
cannabinoids such as THC [77, 78]. Cannabinoid 1 (CB1)
receptors are predominantly expressed throughout the cen-
tral nervous system where they modulate neurotransmitter
1574 J. Sinclair et al.
release; however, they are also present in the pain-modu-
lating areas such as the dorsal root ganglion [ 78], periaq -
ueductal grey, and rostral ventral medulla [ 79, 80]. Addi -
tionally, CB1-mediated analgesia is not solely via nervous
system modulation, but also potentiates anti-inflammatory
effects on mast cells [81]. Cannabinoid 2 (CB2) receptors
are widely expressed in high concentrations throughout the
periphery and immune cells [80], but are also found in lower
amounts in the brain and spinal cord [78]. CB2 receptors
increase in response to peripheral nerve damage, interfere
with inflammatory hyperalgesia, and modulate neuroim-
mune activity [78, 82]. Furthermore, CB2 activation inhibits
proinflammatory signaling released near nociceptive nerves
and can propagate downstream release of opioids [81, 83],
and has demonstrated antinociceptive activity in inflamma-
tory hyperalgesia and neuropathic pain [84, 85].
Focusing on endometriosis as an exemplar, there are sev-
eral drivers for the pain experience, including nociceptive,
inflammatory, and neuropathic pain mechanisms which are
interconnected and complex to manage [ 73]. Additionally,
the psychological impact of the pain experience in people
with endometriosis can cause anxiety and pain catastrophiz-
ing, with the related sequalae of impacting self-esteem and
relationships, worsening the pain experience further [ 73].
Phytocannabinoids from Cannabis spp not only interact
with CB1 and CB2 receptors to exert analgesic activity, but
also modulate transient receptor potential vanilloid (TRPV)
channels which are involved in neuropathic pain signals
[81, 86]. Modulation of serotonin receptors (5HT1A) by
phytocannabinoids such as cannabidiol can assist in pain
through exerting anxiolytic and antidepressant activity, and
other antinociceptive effects of cannabinoids have been pro-
posed specific to endometriosis, including antiangiogenic,
immunomodulating, and antiproliferative activities [81,
87, 88].Whilst more research is needed to fully elucidate
the efficacy and safety of cannabis and cannabinoid-based
medicinal products in endometriosis and other gynecologi-
cal conditions, recent changes in regulatory scheduling of
cannabis has opened up this field of research to the broader
international scientific community.
4 Access to Medicinal Cannabis
With the enactment of the Compassionate Use Act (Propo-
sition 215) in 1996, California became the first US state
to permit legal access to cannabis for medical reasons
under physician supervision [48]. This started a ripple
effect throughout the USA, with 37 states allowing legal-
ized medicinal cannabis, including seven states allowing
access to CBD-containing products only. In contrast, Canada
adopted the Marijuana Medical Access Regulations in 2001
that was replaced by the Marijuana for Medical Purposes
Regulations in 2014 with no restrictions on the clinical indi-
cations for which cannabis could be prescribed [89]. More
than 50 countries have followed suit, adopting assorted
medicinal cannabis regulatory models [90], including Israel,
the United Kingdom, Australia, and New Zealand. Different
nations have varying degrees of regulatory oversight and
product quality assurance standards. Changes to laws and
regulations have also allowed the scientific community to
research cannabis more rigorously and allowed people with
gynecological pain to access cannabis legally for medicinal
purposes.
5 Evidence for Gynecological Pain
Conditions
Currently there are few properly designed and controlled
randomized clinical trials investigating the efficacy of can-
nabis for gynecological symptoms, which limits clear guid-
ance around clinical recommendations. Until such studies
are undertaken, there is a reliance on evidence that is lower
on the evidence pyramid, supported by a growing body of
retrospective data, cohort studies, and surveys, reporting
the positive effects of cannabis from patients with gyneco-
logical symptoms [91]. Given poor symptom management
[15], long waiting times for endometriosis surgery in some
jurisdictions [29], and side effects of many medications for
pelvic pain [26], it is perhaps unsurprising that people with
CPP are using cannabis as a substitute for, or in addition to,
more orthodox treatments. A cross-sectional survey of 240
CPP patients recruited in an outpatient gynecology office
reported that one-quarter of patients with CPP used can -
nabis regularly as an adjunct to prescribed medicines, with
96% reporting improvements in their symptoms, including
84% reporting improved muscle pain, 72% a reduction in
irritability, depression, and anxiety, and 68% an improve-
ment in sleep [92]. Similarly, a cross-sectional survey of 484
endometriosis patients in Australia on self-management of
endometriosis reported illicit cannabis was the most effec-
tive self-management strategy [93]. In this survey, one in
ten respondents reported utilizing illicit cannabis for thera-
peutic purposes to manage their endometriosis symptoms,
with self-reported pain reduction rated at 7.6/10. In addi-
tion, over half (56%) of the cohort reported a 50% or more
reduction in pharmaceutical medications typically used for
endometriosis management [ 93, 94]. From a retrospective,
electronic record-based cohort study of 252 patients with
self-reported endometriosis, cannabis use for decreasing
pelvic pain was described, with inhaled delivery being the
most common mode of administration [95]. This prefer -
ence for inhalation may be due to the rapid speed of onset
of pharmacological effects for inhaled cannabis compared
with oral forms [ 96], which could provide better control
1575
Cannabis for Gynecological Conditions
for the sudden breakthrough pain that commonly occurs in
endometriosis (so called ‘endo flares’). This study also sug-
gested improvements in comorbid symptoms such as mood
and gastrointestinal symptoms, common in those with endo-
metriosis [19], and had greater improvement for oral dosage
forms compared with inhaled [95], suggesting that tailoring
the mode of administration to target specific symptoms is
an important clinical consideration. During the COVID-19
pandemic, an international cross-sectional survey found that
51% of 1634 respondents with endometriosis used cannabis
in the 3 months prior [97]. Respondents with legal access
were more likely to consume cannabis than those without
and were also more likely to disclose their usage to health-
care professionals. In many of these studies, a deprescribing
or ‘substitution effect’ is reported where uptake in cannabis
usage results in a reduction in one or more pharmaceuti-
cals [94]. From a cross-sectional study of 213 participants
in New Zealand, illicit cannabis use for managing pain
and to improve sleep was reported in 95% of respondents,
with over 80% (n = 176/213) indicating that cannabis had
reduced their normal pharmaceutical medication usage [98].
Almost two-thirds (n = 128/213) of respondents completely
stopped a medication, most commonly analgesics (66%,
n = 85/128), with opioids (40%, n = 51/128) being the most
common analgesic stopped, followed by NSAIDs at 17%
(n = 21/128), antidepressants (16%, n = 20/128), and ben-
zodiazepines (15%, n = 9/128) [98]. In a separate study from
Australia and New Zealand, 237 people with endometriosis
reported substantial substitution effects utilizing predomi-
nantly illicit cannabis [99], with a 50% or more reduction in
usage being reported for those who currently or previously
used opioid analgesia (66%, n = 121/183), non-opioid anal-
gesia (63%, n = 147/233), neuroleptics (61%, n = 37/60),
and anxiolytic medications (47.9%, n = 46/96).
6 Risks of Cannabis Usage
Cannabis use for gynecological pain, whether legal or illicit,
is not without side effects or risks [100]. Factors such as
early age of initiation associated with mental ill health in
vulnerable populations, dependence, and abuse potential
(i.e., particularly THC-dominant cannabis) are important
clinical considerations for clinicians to discuss with their
patients before prescribing or recommending medicinal can-
nabis [96, 100]. The most common side effects reported by
cannabis consumers in general include dry mouth, anxiety,
nausea, dizziness, drowsiness/fatigue, and cognitive effects
[96]. These are similar to those reported by people using
cannabis for gynecological pain; 84% of those using can -
nabis for pelvic pain reported side effects, most commonly
dry mouth, sleepiness, and feeling ‘high’ [92]. In those with
endometriosis, just under a third (28%) of cannabis users
reported side effects; 75% reported feelings of euphoria,
72% increased appetite, 67% dry mouth, and 35% feelings
of mild anxiety or paranoia with medically diagnosed can-
nabis; hyperemesis syndrome was reported by only two
respondents (<1%) [97]. However, cessation due to these
side effects is relatively low, with just under 23% of those
who reported cessation of cannabis indicated it was due to
side effects [97].
Deprescribing associated with cannabis substitution is
promising. However, research suggests that people are not
informing their medical doctor of their use of illicit cannabis
for therapeutic purposes, citing concerns over legal reper -
cussions (combined 31.3%), societal judgment (29.2%), the
doctor’s reaction (29.2%), or the doctor’s presumed unwill-
ingness to prescribe (10.4%). This is concerning as many
of the medications that are being reduced or discontinued,
such as opioids and benzodiazepines, have potential for sig-
nificant withdrawal [101, 102] if not tapered off correctly
under medical supervision. Therefore, doctors who work
with patients with endometriosis or other forms of chronic
pelvic pain should be aware of the likelihood of potential
cannabis usage, and try to encourage disclosure of usage,
or at minimum, closely monitor usage of these medications
over time.
7 Barriers to Usage
Whilst the distinct lack of randomized clinical trial data may
be a significant barrier to cannabis adoption for gynecological
pain conditions such as CPP and endometriosis, there may be
more pernicious obstacles. The deleterious impact of stigma
is well described in the medicinal cannabis cohort, and whilst
some have proposed that stigma is diminishing due to normali-
zation in certain localities, there is little evidence to suggest
it has disappeared [103]. Recent data from the UK of 2319
patients utilizing cannabis-based medicines (CBMs) indicated
that participants were afraid of what the police or criminal
justice system (57.1%), other government agencies (55.3%),
and healthcare professionals (40.2%) might think about their
treatment choice, suggestive of a high prevalence of perceived
stigma [104]. Qualitative research of people utilizing illicit
cannabis for therapeutic purposes shows that stigmatization
is related to, and perpetuated by, the ambiguous status of can-
nabis (i.e., both a legal medicine and illegal drug) and the lack
of knowledge about medical cannabis amongst police, medical
professionals, and the general public [105]. Additional qualita-
tive research exploring the barriers, drivers and perceptions
of cannabis use for primary dysmenorrhea (PD) in Australian
women [106] goes further, showing that the perceived dam-
age to their professional and social standing if their cannabis
use became known was a serious concern, despite its legality
for medical purposes. Participants spoke about the clandestine
1576 J. Sinclair et al.
way they had to consume cannabis for their pain and symp-
toms, and that even the possibility of being perceived as irre-
sponsible, simply by virtue of being a cannabis user, was a
significant barrier to adoption [106]. Stigma not only impacts
people directly, but also indirectly in the bias and opinions
of the healthcare professionals they interact with. Surveyed
pharmacists have highlighted the impact that stigma can have
on patients, with the lack of public awareness and inability
to distinguish between medicinal and recreational cannabis
identified as key factors contributing to public stigma [107,
108]. Furthermore, effective treatment with medicinal canna-
bis may be compromised by negative attitudes, stigmatized
perceptions, and subjective norms of nurses and physicians
[109], highlighting that health education for both health pro-
fessionals and the general public plays a crucial role in reduc-
ing the impact of stigma [110]. This is particularly detrimental
given that women with CPP and associated conditions such as
endometriosis already experience stigma and discrimination
[111, 112].
The impact of such stigma permeates into government
laws and corporate policies, notably drug-driving laws
and workplace drug testing policies [113, 114]. This is a
significant challenge as cannabis is one or more of (a) a
legal medicine, (b) a recreational/adult-use drug, and (c) an
illicit/illegal substance, depending on geographic location
and legal jurisdiction. This is reflected in the haze of issues
with preexisting drug-driving laws and workplace policies.
Whilst road safety risks associated with the medicinal use of
cannabis appear to be similar or lower than other potentially
impairing prescription medications [90], including those
commonly used in endometriosis such as opioids, in coun-
tries such as Australia, patients utilizing medicinal cannabis
are still subject to drug-driving testing, which detects for
presence of THC alone, not impairment. Such laws crimi-
nalize the presence of THC in body fluids irrespective of
impairment and appears to be linked to the historical status
of cannabis as a Schedule 9 substance with no recognized
medical value [90]. Research has shown, particularly in
those living in regional and remote locations, that facing
such criminal prosecution for driving whilst using canna-
bis legally as a medicine is a significant barrier to adoption
[106], giving rise to the need for updated drug-driving laws.
Similarly, workers in high-risk industries such as defense,
construction, railroad, transport, maritime, and mining oper-
ations are similarly disadvantaged as these occupations are
usually subjected to workplace drug testing policies [49].
8 Illicit versus Legal Medicinal Cannabis
Illicit cannabis is unlikely to have any accurate indication of
the level of THC, and the lack of any quality control precludes
consistency, making consistent dosing for medical purposes
next to impossible. Medicinal cannabis undergoes rigorous
testing procedures including microbial limits, cannabinoid
standardization, detection of foreign matter, aflatoxins, ochra-
toxin A, pesticide and solvent residues. This ability to culti-
vate and standardize cannabinoids and manufacture medicinal
cannabis products to high quality standards with reproducible