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Wikipedia

Medical cannabis

Medical cannabis, or medical marijuana (MMJ), is cannabis and cannabinoids that are prescribed by physicians for their patients.[1][2] The use of cannabis as medicine has not been rigorously tested due to production and governmental restrictions, resulting in limited clinical research to define the safety and efficacy of using cannabis to treat diseases.[3]

Preliminary evidence has indicated that cannabis might reduce nausea and vomiting during chemotherapy and reduce chronic pain and muscle spasms.[4][5] Regarding non-inhaled cannabis or cannabinoids, a 2021 review found that it provided little relief against chronic pain and sleep disturbance, and caused several transient adverse effects, such as cognitive impairment, nausea, and drowsiness.[6]

Short-term use increases the risk of minor and major adverse effects.[5] Common side effects include dizziness, feeling tired, vomiting, and hallucinations.[5] Long-term effects of cannabis are not clear.[5] Concerns include memory and cognition problems, risk of addiction, schizophrenia in young people, and the risk of children taking it by accident.[4]

Many cultures have used cannabis for therapeutic purposes for thousands of years.[7] Some American medical organizations have requested removal of cannabis from the list of Schedule I controlled substances maintained by the United States federal government, followed by regulatory and scientific review.[8][9] Others oppose its legalization, such as the American Academy of Pediatrics.[10]

Medical cannabis can be administered through various methods, including capsules, lozenges, tinctures, dermal patches, oral or dermal sprays, cannabis edibles, and vaporizing. Synthetic cannabinoids are available for prescription use in some countries, such as dronabinol and nabilone. Countries that allow the medical use of whole-plant cannabis include Argentina, Australia, Canada, Chile, Colombia, Germany, Greece, Israel, Italy, the Netherlands, Peru, Poland, Portugal, Spain, and Uruguay. In the United States, 38 states and the District of Columbia have legalized cannabis for medical purposes, beginning with the passage of California's Proposition 215 in 1996.[11] Although cannabis remains prohibited for any use at the federal level, the Rohrabacher–Farr amendment was enacted in December 2014, limiting the ability of federal law to be enforced in states where medical cannabis has been legalized.

Classification

The National Institute on Drug Abuse defines medical cannabis as "using the whole, unprocessed marijuana plant or its basic extracts to treat symptoms of illness and other conditions".[12]

A cannabis plant includes more than 400 different chemicals, of which about 70 are cannabinoids.[13] In comparison, typical government-approved medications contain only one or two chemicals.[13] The number of active chemicals in cannabis is one reason why treatment with cannabis is difficult to classify and study.[13]

A 2014 review stated that the variations in ratio of CBD-to-THC in botanical and pharmaceutical preparations determines the therapeutic vs psychoactive effects (CBD attenuates THC's psychoactive effects[14]) of cannabis products.[15]

Medical uses

 
Cannabis as illustrated in Köhler's Book of Medicinal Plants, 1897

Overall, research into the health effects of medical cannabis has been of low quality and it is not clear whether it is a useful treatment for any condition, or whether harms outweigh any benefit.[16] There is no consistent evidence that it helps with chronic pain and muscle spasms.[16]

Low quality evidence suggests its use for reducing nausea during chemotherapy, improving appetite in HIV/AIDS, improving sleep, and improving tics in Tourette syndrome.[5] When usual treatments are ineffective, cannabinoids have also been recommended for anorexia, arthritis, glaucoma,[17] and migraine.[18]

It is unclear whether American states might be able to mitigate the adverse effects of the opioid epidemic by prescribing medical cannabis as an alternative pain management drug.[19]

Cannabis should not be used in pregnancy.[20]

Nausea and vomiting

Medical cannabis is somewhat effective in chemotherapy-induced nausea and vomiting (CINV)[4][17] and may be a reasonable option in those who do not improve following preferential treatment.[21] Comparative studies have found cannabinoids to be more effective than some conventional antiemetics such as prochlorperazine, promethazine, and metoclopramide in controlling CINV,[22] but these are used less frequently because of side effects including dizziness, dysphoria, and hallucinations.[23][24] Long-term cannabis use may cause nausea and vomiting, a condition known as cannabinoid hyperemesis syndrome (CHS).[25]

A 2016 Cochrane review said that cannabinoids were "probably effective" in treating chemotherapy-induced nausea in children, but with a high side-effect profile (mainly drowsiness, dizziness, altered moods, and increased appetite). Less common side effects were "ocular problems, orthostatic hypotension, muscle twitching, pruritus, vagueness, hallucinations, lightheadedness and dry mouth".[26]

HIV/AIDS

Evidence is lacking for both efficacy and safety of cannabis and cannabinoids in treating patients with HIV/AIDS or for anorexia associated with AIDS. As of 2013, current studies suffer from the effects of bias, small sample size, and lack of long-term data.[27]

Pain

A 2021 review found little effect of using non-inhaled cannabis to relieve chronic pain.[6] According to a 2019 systematic review, there have been inconsistent results of using cannabis for neuropathic pain, spasms associated with multiple sclerosis and pain from rheumatic disorders, but was not effective treating chronic cancer pain. The authors state that additional randomized controlled trials of different cannabis products are necessary to make conclusive recommendations.[16]

When cannabis is inhaled to relieve pain, blood levels of cannabinoids rise faster than when oral products are used, peaking within three minutes and attaining an analgesic effect in seven minutes.[28]

A 2011 review considered cannabis to be generally safe,[29] and it appears safer than opioids in palliative care.[30]

A 2022 review concluded the pain relief experienced after using medical cannabis is due to the placebo effect, especially given widespread media attention that sets the expectation for pain relief.[31]

Neurological conditions

Cannabis' efficacy is not clear in treating neurological problems, including multiple sclerosis (MS) and movement problems.[15] Evidence also suggests that oral cannabis extract is effective for reducing patient-centered measures of spasticity.[15] A trial of cannabis is deemed to be a reasonable option if other treatments have not been effective.[4][by whom?] Its use for MS is approved in ten countries.[4][32][conflicted source?] A 2012 review found no problems with tolerance, abuse, or addiction.[33] In the United States, cannabidiol, one of the cannabinoids found in the marijuana plant, has been approved for treating two severe forms of epilepsy, Lennox-Gastaut syndrome and Dravet syndrome.[34]

Mental disorders

A 2019 systematic review found that there is a lack of evidence that cannabinoids are effective in treating depressive or anxiety disorders, attention-deficit hyperactivity disorder (ADHD), Tourette syndrome, post-traumatic stress disorder, or psychosis.[35]

Adverse effects

 
American medical hashish

Medical use

There is insufficient data to draw strong conclusions about the safety of medical cannabis.[36] Typically, adverse effects of medical cannabis use are not serious;[4] they include tiredness, dizziness, increased appetite, and cardiovascular and psychoactive effects. Other effects can include impaired short-term memory; impaired motor coordination; altered judgment; and paranoia or psychosis at high doses.[37] Tolerance to these effects develops over a period of days or weeks. The amount of cannabis normally used for medicinal purposes is not believed to cause any permanent cognitive impairment in adults, though long-term treatment in adolescents should be weighed carefully as they are more susceptible to these impairments. Withdrawal symptoms are rarely a problem with controlled medical administration of cannabinoids. The ability to drive vehicles or to operate machinery may be impaired until a tolerance is developed.[21] Although supporters of medical cannabis say that it is safe,[36] further research is required to assess the long-term safety of its use.[23][38]

Cognitive effects

Recreational use of cannabis is associated with cognitive deficits, especially for those who begin to use cannabis in adolescence. As of 2021 there is a lack of research into long-term cognitive effects of medical use of cannabis, but one 12-month observational study reported that "MC patients demonstrated significant improvements on measures of executive function and clinical state over the course of 12 months".[39]

Impact on psychosis

Exposure to THC can cause acute transient psychotic symptoms in healthy individuals and people with schizophrenia.[14]

A 2007 meta analysis concluded that cannabis use reduced the average age of onset of psychosis by 2.7 years relative to non-cannabis use.[40] A 2005 meta analysis concluded that adolescent use of cannabis increases the risk of psychosis, and that the risk is dose-related.[41] A 2004 literature review on the subject concluded that cannabis use is associated with a two-fold increase in the risk of psychosis, but that cannabis use is "neither necessary nor sufficient" to cause psychosis.[42] A French review from 2009 came to a conclusion that cannabis use, particularly that before age 15, was a factor in the development of schizophrenic disorders.[43]

Pharmacology

The genus Cannabis contains two species which produce useful amounts of psychoactive cannabinoids: Cannabis indica and Cannabis sativa, which are listed as Schedule I medicinal plants in the US;[4] a third species, Cannabis ruderalis, has few psychogenic properties.[4] Cannabis contains more than 460 compounds;[7] at least 80 of these are cannabinoids[44][45]chemical compounds that interact with cannabinoid receptors in the brain.[4] As of 2012, more than 20 cannabinoids were being studied by the U.S. FDA.[46]

The most psychoactive cannabinoid found in the cannabis plant is tetrahydrocannabinol (or delta-9-tetrahydrocannabinol, commonly known as THC).[7] Other cannabinoids include delta-8-tetrahydrocannabinol, cannabidiol (CBD), cannabinol (CBN), cannabicyclol (CBL), cannabichromene (CBC) and cannabigerol (CBG); they have less psychotropic effects than THC, but may play a role in the overall effect of cannabis.[7] The most studied are THC, CBD and CBN.[47]

CB1 and CB2 are the primary cannabinoid receptors responsible for several of the effects of cannabinoids, although other receptors may play a role as well. Both belong to a group of receptors called G protein-coupled receptors (GPCRs). CB1 receptors are found in very high levels in the brain and are thought to be responsible for psychoactive effects.[48] CB2 receptors are found peripherally throughout the body and are thought to modulate pain and inflammation.[49]

Absorption

Cannabinoid absorption is dependent on its route of administration.

Inhaled and vaporized THC have similar absorption profiles to smoked THC, with a bioavailability ranging from 10 to 35%. Oral administration has the lowest bioavailability of approximately 6%, variable absorption depending on the vehicle used, and the longest time to peak plasma levels (2 to 6 hours) compared to smoked or vaporized THC.[50]

Similar to THC, CBD has poor oral bioavailability, approximately 6%. The low bioavailability is largely attributed to significant first-pass metabolism in the liver and erratic absorption from the gastrointestinal tract. However, oral administration of CBD has a faster time to peak concentrations (2 hours) than THC.[50]

Due to the poor bioavailability of oral preparations, alternative routes of administration have been studied, including sublingual and rectal. These alternative formulations maximize bioavailability and reduce first-pass metabolism. Sublingual administration in rabbits yielded bioavailability of 16% and time to peak concentration of 4 hours.[51] Rectal administration in monkeys doubled bioavailability to 13.5% and achieved peak blood concentrations within 1 to 8 hours after administration.[52]

Distribution

Like cannabinoid absorption, distribution is also dependent on route of administration. Smoking and inhalation of vaporized cannabis have better absorption than do other routes of administration, and therefore also have more predictable distribution.[52][53] THC is highly protein bound once absorbed, with only 3% found unbound in the plasma. It distributes rapidly to highly vascularized organs such as the heart, lungs, liver, spleen, and kidneys, as well as to various glands. Low levels can be detected in the brain, testes, and unborn fetuses, all of which are protected from systemic circulation via barriers.[54] THC further distributes into fatty tissues a few days after administration due to its high lipophilicity, and is found deposited in the spleen and fat after redistribution.[53][55][56]

Metabolism

Delta-9-THC is the primary molecule responsible for the effects of cannabis. Delta-9-THC is metabolized in the liver and turns into 11-OH-THC.[57] 11-OH-THC is the first metabolic product in this pathway. Both Delta-9-THC and 11-OH-THC are psychoactive. The metabolism of THC into 11-OH-THC plays a part in the heightened psychoactive effects of edible cannabis.[58]

Next, 11-OH-THC is metabolized in the liver into 11-COOH-THC, which is the second metabolic product of THC.[59] 11-COOH-THC is not psychoactive.[57]

Ingestion of edible cannabis products lead to a slower onset of effect than the inhalation of it because the THC travels to the liver first through the blood before it travels to the rest of the body. Inhaled cannabis can result in THC going directly to the brain, where it then travels from the brain back to the liver in recirculation for metabolism.[57] Eventually, both routes of metabolism result in the metabolism of psychoactive THC to inactive 11-COOH-THC.

Excretion

Due to substantial metabolism of THC and CBD, their metabolites are excreted mostly via feces, rather than by urine.[50][60] After delta-9-THC is hydroxylated into 11-OH-THC via CYP2C9, CYP2C19, and CYP3A4, it undergoes phase II metabolism into more than 30 metabolites, a majority of which are products of glucuronidation. Approximately 65% of THC is excreted in feces and 25% in the urine, while the remaining 10% is excreted by other means.[50] The terminal half-life of THC is 25 to 36 hours,[61] whereas for CBD it is 18 to 32 hours.[60]

CBD is hydroxylated by P450 liver enzymes into 7-OH-CBD. Its metabolites are products of primarily CYP2C19 and CYP3A4 activity, with potential activity of CYP1A1, CYP1A2, CYP2C9, and CYP2D6.[62] Similar to delta-9-THC, a majority of CBD is excreted in feces and some in the urine.[50] The terminal half-life is approximately 18–32 hours.[63]

Administration

 
Illustrating various forms of medicinal cannabis

Smoking has been the means of administration of cannabis for many users, but it is not suitable for the use of cannabis as a medicine.[64] It was the most common method of medical cannabis consumption in the US as of 2013.[4] It is difficult to predict the pharmacological response to cannabis because concentration of cannabinoids varies widely, as there are different ways of preparing it for consumption (smoked, applied as oils, eaten, infused into other foods, or drunk) and a lack of production controls.[4] The potential for adverse effects from smoke inhalation makes smoking a less viable option than oral preparations.[64] Cannabis vaporizers have gained popularity because of a perception among users that fewer harmful chemicals are ingested when components are inhaled via aerosol rather than smoke.[4] Cannabinoid medicines are available in pill form (dronabinol and nabilone) and liquid extracts formulated into an oromucosal spray (nabiximols).[4] Oral preparations are "problematic due to the uptake of cannabinoids into fatty tissue, from which they are released slowly, and the significant first-pass liver metabolism, which breaks down Δ9THC and contributes further to the variability of plasma concentrations".[64]

The US Food and Drug Administration (FDA) has not approved smoked cannabis for any condition or disease, as it deems that evidence is lacking concerning safety and efficacy.[65] The FDA issued a 2006 advisory against smoked medical cannabis stating: "marijuana has a high potential for abuse, has no currently accepted medical use in treatment in the United States, and has a lack of accepted safety for use under medical supervision."[65]

History

Ancient

Cannabis, called 麻 (meaning "hemp; cannabis; numbness") or dàmá 大麻 (with "big; great") in Chinese, was used in Taiwan for fiber starting about 10,000 years ago.[66] The botanist Hui-lin Li wrote that in China, "The use of Cannabis in medicine was probably a very early development. Since ancient humans used hemp seed as food, it was quite natural for them to also discover the medicinal properties of the plant."[67] Emperor Shen-Nung, who was also a pharmacologist, wrote a book on treatment methods in 2737 BCE that included the medical benefits of cannabis. He recommended the substance for many ailments, including constipation, gout, rheumatism, and absent-mindedness.[68] Cannabis is one of the 50 "fundamental" herbs in traditional Chinese medicine.[69]

The Ebers Papyrus (c. 1550 BCE) from Ancient Egypt describes medical cannabis.[70] The ancient Egyptians used hemp (cannabis) in suppositories for relieving the pain of hemorrhoids.[71]

Surviving texts from ancient India confirm that cannabis' psychoactive properties were recognized, and doctors used it for treating a variety of illnesses and ailments, including insomnia, headaches, gastrointestinal disorders, and pain, including during childbirth.[72]

The Ancient Greeks used cannabis to dress wounds and sores on their horses,[73] and in humans, dried leaves of cannabis were used to treat nose bleeds, and cannabis seeds were used to expel tapeworms.[73]

In the medieval Islamic world, Arabic physicians made use of the diuretic, antiemetic, antiepileptic, anti-inflammatory, analgesic and antipyretic properties of Cannabis sativa, and used it extensively as medication from the 8th to 18th centuries.[74]

Landrace strains

 
Evolution of cultivated cannabis strains. The cultivar, Cannabis ruderalis, still grows wild today.

Cannabis seeds may have been used for food, rituals or religious practices in ancient Europe and China.[75]: 19–22  Harvesting the plant led to the spread of cannabis throughout Eurasia about 10,000 to 5,000 years ago, with further distribution to the Middle East and Africa about 2,000 to 500 years ago.[75]: 18–19  A landrace strain of cannabis developed over centuries.[76] They are cultivars of the plant that originated in one specific region.

Widely cultivated strains of cannabis, such as "Afghani" or "Hindu Kush", are indigenous to the Pakistan and Afghanistan regions, while "Durban Poison" is native to Africa.[75]: 45–48  There are approximately 16 landrace strains of cannabis identified from Pakistan, Jamaica, Africa, Mexico, Central America and Asia.[77]

Modern

An Irish physician, William Brooke O'Shaughnessy, is credited with introducing cannabis to Western medicine.[78] O'Shaughnessy discovered cannabis in the 1830s while living abroad in India, where he conducted numerous experiments investigating the drug's medical utility (noting in particular its analgesic and anticonvulsant effects).[79] He returned to England with a supply of cannabis in 1842, after which its use spread through Europe and the United States.[80] In 1845 French physician Jacques-Joseph Moreau published a book about the use of cannabis in psychiatry.[81] In 1850 cannabis was entered into the United States Pharmacopeia.[79] An anecdotal report of Cannabis indica as a treatment for tetanus appeared in Scientific American in 1880.[82]

The use of cannabis in medicine began to decline by the end of the 19th century, due to difficulty in controlling dosages and the rise in popularity of synthetic and opium-derived drugs.[80] Also, the advent of the hypodermic syringe allowed these drugs to be injected for immediate effect, in contrast to cannabis which is not water-soluble and therefore cannot be injected.[80]

In the United States, the medical use of cannabis further declined with the passage of the Marihuana Tax Act of 1937, which imposed new regulations and fees on physicians prescribing cannabis.[83] Cannabis was removed from the U.S. Pharmacopeia in 1941, and officially banned for any use with the passage of the Controlled Substances Act of 1970.[80]

Cannabis began to attract renewed interest as medicine in the 1970s and 1980s, in particular due to its use by cancer and AIDS patients who reported relief from the effects of chemotherapy and wasting syndrome.[84] In 1996, California became the first U.S. state to legalize medical cannabis in defiance of federal law.[85] In 2001, Canada became the first country to adopt a system regulating the medical use of cannabis.[86]

Society and culture

Legal status

 
Legal status of (whole-plant) medical cannabis worldwide
  Legal as authorized by a physician
  Legal for any use (no prescription required)

See also countries that have decriminalized or where enforcement is limited.

Countries that have legalized the medical use of cannabis include Argentina,[87] Australia,[88] Brazil,[89] Canada,[90] Chile,[90] Colombia,[90] Costa Rica,[91] Croatia,[92] Cyprus,[93] Czech Republic,[90] Finland,[94] Germany,[95] Greece,[96] Israel,[97] Italy,[98] Jamaica,[99] Lebanon,[100] Luxembourg,[101] Malta,[102] Morocco,[103] the Netherlands,[90] New Zealand,[104] North Macedonia,[105] Panama,[106] Peru,[107] Poland,[108] Portugal,[109] Rwanda,[110] Spain,[111] Sri Lanka,[112] Switzerland,[113] Thailand,[114] the United Kingdom,[115] and Uruguay.[90] Other countries have more restrictive laws that allow only the use of isolated cannabinoid drugs such as Sativex or Epidiolex.[116][117] Countries with the most relaxed policies include Canada,[118] the Netherlands,[90] Thailand,[119] and Uruguay,[90] where cannabis can be purchased without need for a prescription. In Mexico, THC content of medical cannabis is limited to one percent.[120] In the United States, the legality of medical cannabis varies by state.[11]

Cannabis and its derivatives are subject to regulation under three United Nations treaties: the 1961 Single Convention on Narcotic Drugs, the 1971 Convention on Psychotropic Substances, and the 1988 Convention Against Illicit Traffic in Narcotic Drugs and Psychotropic Substances.[121] Cannabis is classified as a Schedule I drug under the Single Convention treaty, meaning that medical use is allowed but that it is considered to be an addictive drug with a serious risk of abuse – along with other drugs such as opium and cocaine.[122] Prior to December 2020 it was also included in Schedule IV, a subset of Schedule I, which is for only the most dangerous drugs such as heroin and fentanyl.[123] Member nations of the UN Commission on Narcotic Drugs voted 27–25 to remove it from Schedule IV on 2 December 2020,[124] following a World Health Organization recommendation for removal in January 2019.[125][126]

United States

In the United States, the use of cannabis for medical purposes is legal in 38 states, four out of five permanently inhabited U.S. territories, and the District of Columbia.[11] An additional 10 states have more restrictive laws allowing the use of low-THC products.[11] Cannabis remains illegal at the federal level under the Controlled Substances Act, which classifies it as a Schedule I drug with a high potential for abuse and no accepted medical use. In December 2014, however, the Rohrabacher–Farr amendment was signed into law, prohibiting the Justice Department from prosecuting individuals acting in accordance with state medical cannabis laws.[127]

Economics

Distribution

 
Medical marijuana dispensary in Denver, Colorado

The method of obtaining medical cannabis varies by region and by legislation. In the US, most consumers grow their own or buy it from cannabis dispensaries in states where it is legal.[4][128] Marijuana vending machines for selling or dispensing cannabis are in use in the United States and are planned to be used in Canada.[129] In 2014, the startup Meadow began offering on-demand delivery of medical marijuana in the San Francisco Bay Area, through their mobile app.[130]

Almost 70% of medical cannabis is exported from the United Kingdom, according to a 2017 United Nations report, with much of the remaining amount coming from Canada and the Netherlands.[131]

Insurance

In the United States, health insurance companies may not pay for a medical marijuana prescription as the Food and Drug Administration must approve any substance for medicinal purposes. Before this can happen, the FDA must first permit the study of the medical benefits and drawbacks of the substance, which it has not done since it was placed on Schedule I of the Controlled Substances Act in 1970. Therefore, all expenses incurred fulfilling a medical marijuana prescription will possibly be incurred as out-of-pocket.[132] However, the New Mexico Court of Appeals has ruled that workers' compensation insurance must pay for prescribed marijuana as part of the state's Medical Cannabis Program.[133]

Positions of medical organizations

Medical organizations that have issued statements in support of allowing access to medical cannabis include the American Nurses Association,[8] American Public Health Association,[134] American Medical Student Association,[135] National Multiple Sclerosis Society,[136] Epilepsy Foundation,[137] and Leukemia & Lymphoma Society.[138]

Organizations that oppose the legalization of medical cannabis include the American Academy of Pediatrics[10] and American Psychiatric Association.[139] However, the AAP also supports rescheduling for the purpose of facilitating research.[10]

The American Medical Association[140] and American College of Physicians[141] do not take a position on the legalization of medical cannabis, but have called for the Schedule I classification to be reviewed. The American Academy of Family Physicians[9] and American Society of Addiction Medicine[142] also do not take a position, but do support rescheduling to better facilitate research. The American Heart Association says that "many of the concerning health implications of cannabis include cardiovascular diseases" but that it supports rescheduling to allow "more nuanced ... marijuana legislation and regulation" and to "reflect the existing science behind cannabis".[143] The American Cancer Society[144] and American Psychological Association[145] have noted the obstacles that exist for conducting research on cannabis, and have called on the federal government to better enable scientific study of the drug.

Cancer Research UK say that while cannabis is being studied for therapeutic potential, "claims that there is solid "proof" that cannabis or cannabinoids can cure cancer is highly misleading to patients and their families, and builds a false picture of the state of progress in this area".[146]

Brand names

In the US, the FDA has approved two oral cannabinoids for use as medicine: dronabinol and nabilone.[4] Dronabinol, synthetic THC, is listed as Schedule II.[147] Nabilone, a synthetic cannabinoid, is also Schedule II, indicating high potential for side effects and addiction.[46] Both received approval for sale in the US in 1985, under the brand names Marinol and Cesamet.[148] Nabiximols, an oromucosal spray derived from two strains of Cannabis sativa and containing THC and CBD,[46] is not approved in the United States, but is approved in several European countries, Canada, and New Zealand as of 2013.[4] As of 2018, medical marijuana in Canada is being legally distributed to registered patients in bud, drops and capsule forms by such companies as Canopy Growth Corp. and Aurora Cannabis.

Generic
medication
Brand
name(s)
Country Licensed indications
Nabilone Cesamet U.S., Canada Antiemetic (treatment of nausea or vomiting) associated with chemotherapy that has failed to respond adequately to conventional therapy[4]
Dronabinol Marinol
Syndros U.S. Anorexia associated with AIDS–related weight loss[4]
Nabiximols Sativex Canada, New Zealand,
majority of the EU[149]
Limited treatment for spasticity and neuropathic pain associated with multiple sclerosis and intractable cancer pain.[4]

As an antiemetic, these medications are usually used when conventional treatment for nausea and vomiting associated with cancer chemotherapy fail to work.[4]

Nabiximols is used for treatment of spasticity associated with MS when other therapies have not worked, and when an initial trial demonstrates "meaningful improvement".[4] Trials for FDA approval in the US are underway.[4] It is also approved in several European countries for overactive bladder and vomiting.[46] When sold under the trade name Sativex as a mouth spray, the prescribed daily dose in Sweden delivers a maximum of 32.4 mg of THC and 30 mg of CBD; mild to moderate dizziness is common during the first few weeks.[150]

Relative to inhaled consumption, peak concentration of oral THC is delayed, and it may be difficult to determine optimal dosage because of variability in patient absorption.[4]

In 1964, Albert Lockhart and Manley West began studying the health effects of traditional cannabis use in Jamaican communities. They developed, and in 1987 gained permission to market, the pharmaceutical "Canasol", one of the first cannabis extracts.[151]

Research

Medical cannabis research includes any medical research on using cannabis as a treatment for any medical condition. For reasons including increased popular support of cannabis use, a trend of cannabis legalization, and the perception of medical usefulness, more scientists are doing medical cannabis research. Medical cannabis is broad for many conditions, each of which has its own state of research.

A 2022 review concluded that "oral, synthetic cannabis products with high THC-to-CBD ratios and sublingual, extracted cannabis products with comparable THC-to-CBD ratios may be associated with short-term improvements in chronic pain and increased risk for dizziness and sedation."[152]

See also

References

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Further reading

  • National Academies Of Sciences, Engineering; Health Medicine, Division; Board on Population Health Public Health Practice; Committee on the Health Effects of Marijuana: An Evidence Review Research Agenda (2017). The Health Effects of Cannabis and Cannabinoids: The Current State of Evidence and Recommendations for Research. National Academies of Sciences, Engineering, and Medicine: The National Academies Press. doi:10.17226/24625. ISBN 978-0-309-45304-2. PMID 28182367. from the original on 14 July 2020. Retrieved 7 February 2017. {{cite book}}: |website= ignored (help)  

External links

  • Medical cannabis at Curlie, links to websites about medical cannabis
  • Information on Cannabis and Cannabinoids from the U.S. National Cancer Institute
  • Information on cannabis (marihuana, marijuana) and the cannabinoids from Health Canada
  • Medical Marijuana – a 2014–2015 three-part CNN documentary produced by Sanjay Gupta
  • Marijuana and Medical Marijuana collected news and commentary at The New York Times

medical, cannabis, other, uses, cannabis, cannabis, disambiguation, medical, marijuana, redirects, here, company, medical, marijuana, medical, marijuana, cannabis, cannabinoids, that, prescribed, physicians, their, patients, cannabis, medicine, been, rigorousl. For other uses of Cannabis see Cannabis disambiguation Medical marijuana redirects here For the company see Medical Marijuana Inc Medical cannabis or medical marijuana MMJ is cannabis and cannabinoids that are prescribed by physicians for their patients 1 2 The use of cannabis as medicine has not been rigorously tested due to production and governmental restrictions resulting in limited clinical research to define the safety and efficacy of using cannabis to treat diseases 3 Preliminary evidence has indicated that cannabis might reduce nausea and vomiting during chemotherapy and reduce chronic pain and muscle spasms 4 5 Regarding non inhaled cannabis or cannabinoids a 2021 review found that it provided little relief against chronic pain and sleep disturbance and caused several transient adverse effects such as cognitive impairment nausea and drowsiness 6 Short term use increases the risk of minor and major adverse effects 5 Common side effects include dizziness feeling tired vomiting and hallucinations 5 Long term effects of cannabis are not clear 5 Concerns include memory and cognition problems risk of addiction schizophrenia in young people and the risk of children taking it by accident 4 Many cultures have used cannabis for therapeutic purposes for thousands of years 7 Some American medical organizations have requested removal of cannabis from the list of Schedule I controlled substances maintained by the United States federal government followed by regulatory and scientific review 8 9 Others oppose its legalization such as the American Academy of Pediatrics 10 Medical cannabis can be administered through various methods including capsules lozenges tinctures dermal patches oral or dermal sprays cannabis edibles and vaporizing Synthetic cannabinoids are available for prescription use in some countries such as dronabinol and nabilone Countries that allow the medical use of whole plant cannabis include Argentina Australia Canada Chile Colombia Germany Greece Israel Italy the Netherlands Peru Poland Portugal Spain and Uruguay In the United States 38 states and the District of Columbia have legalized cannabis for medical purposes beginning with the passage of California s Proposition 215 in 1996 11 Although cannabis remains prohibited for any use at the federal level the Rohrabacher Farr amendment was enacted in December 2014 limiting the ability of federal law to be enforced in states where medical cannabis has been legalized Contents 1 Classification 2 Medical uses 2 1 Nausea and vomiting 2 2 HIV AIDS 2 3 Pain 2 4 Neurological conditions 2 5 Mental disorders 3 Adverse effects 3 1 Medical use 3 2 Cognitive effects 3 3 Impact on psychosis 4 Pharmacology 4 1 Absorption 4 2 Distribution 4 3 Metabolism 4 4 Excretion 5 Administration 6 History 6 1 Ancient 6 2 Landrace strains 6 3 Modern 7 Society and culture 7 1 Legal status 7 1 1 United States 7 2 Economics 7 2 1 Distribution 7 2 2 Insurance 7 3 Positions of medical organizations 7 4 Brand names 8 Research 9 See also 10 References 11 Further reading 12 External linksClassificationThe National Institute on Drug Abuse defines medical cannabis as using the whole unprocessed marijuana plant or its basic extracts to treat symptoms of illness and other conditions 12 A cannabis plant includes more than 400 different chemicals of which about 70 are cannabinoids 13 In comparison typical government approved medications contain only one or two chemicals 13 The number of active chemicals in cannabis is one reason why treatment with cannabis is difficult to classify and study 13 A 2014 review stated that the variations in ratio of CBD to THC in botanical and pharmaceutical preparations determines the therapeutic vs psychoactive effects CBD attenuates THC s psychoactive effects 14 of cannabis products 15 Medical uses nbsp Cannabis as illustrated in Kohler s Book of Medicinal Plants 1897Overall research into the health effects of medical cannabis has been of low quality and it is not clear whether it is a useful treatment for any condition or whether harms outweigh any benefit 16 There is no consistent evidence that it helps with chronic pain and muscle spasms 16 Low quality evidence suggests its use for reducing nausea during chemotherapy improving appetite in HIV AIDS improving sleep and improving tics in Tourette syndrome 5 When usual treatments are ineffective cannabinoids have also been recommended for anorexia arthritis glaucoma 17 and migraine 18 It is unclear whether American states might be able to mitigate the adverse effects of the opioid epidemic by prescribing medical cannabis as an alternative pain management drug 19 Cannabis should not be used in pregnancy 20 Nausea and vomiting Medical cannabis is somewhat effective in chemotherapy induced nausea and vomiting CINV 4 17 and may be a reasonable option in those who do not improve following preferential treatment 21 Comparative studies have found cannabinoids to be more effective than some conventional antiemetics such as prochlorperazine promethazine and metoclopramide in controlling CINV 22 but these are used less frequently because of side effects including dizziness dysphoria and hallucinations 23 24 Long term cannabis use may cause nausea and vomiting a condition known as cannabinoid hyperemesis syndrome CHS 25 A 2016 Cochrane review said that cannabinoids were probably effective in treating chemotherapy induced nausea in children but with a high side effect profile mainly drowsiness dizziness altered moods and increased appetite Less common side effects were ocular problems orthostatic hypotension muscle twitching pruritus vagueness hallucinations lightheadedness and dry mouth 26 HIV AIDS Evidence is lacking for both efficacy and safety of cannabis and cannabinoids in treating patients with HIV AIDS or for anorexia associated with AIDS As of 2013 current studies suffer from the effects of bias small sample size and lack of long term data 27 Pain A 2021 review found little effect of using non inhaled cannabis to relieve chronic pain 6 According to a 2019 systematic review there have been inconsistent results of using cannabis for neuropathic pain spasms associated with multiple sclerosis and pain from rheumatic disorders but was not effective treating chronic cancer pain The authors state that additional randomized controlled trials of different cannabis products are necessary to make conclusive recommendations 16 When cannabis is inhaled to relieve pain blood levels of cannabinoids rise faster than when oral products are used peaking within three minutes and attaining an analgesic effect in seven minutes 28 A 2011 review considered cannabis to be generally safe 29 and it appears safer than opioids in palliative care 30 A 2022 review concluded the pain relief experienced after using medical cannabis is due to the placebo effect especially given widespread media attention that sets the expectation for pain relief 31 Neurological conditions Cannabis efficacy is not clear in treating neurological problems including multiple sclerosis MS and movement problems 15 Evidence also suggests that oral cannabis extract is effective for reducing patient centered measures of spasticity 15 A trial of cannabis is deemed to be a reasonable option if other treatments have not been effective 4 by whom Its use for MS is approved in ten countries 4 32 conflicted source A 2012 review found no problems with tolerance abuse or addiction 33 In the United States cannabidiol one of the cannabinoids found in the marijuana plant has been approved for treating two severe forms of epilepsy Lennox Gastaut syndrome and Dravet syndrome 34 Mental disorders Further information Posttraumatic stress disorder Cannabinoids A 2019 systematic review found that there is a lack of evidence that cannabinoids are effective in treating depressive or anxiety disorders attention deficit hyperactivity disorder ADHD Tourette syndrome post traumatic stress disorder or psychosis 35 Adverse effects nbsp American medical hashishMedical use There is insufficient data to draw strong conclusions about the safety of medical cannabis 36 Typically adverse effects of medical cannabis use are not serious 4 they include tiredness dizziness increased appetite and cardiovascular and psychoactive effects Other effects can include impaired short term memory impaired motor coordination altered judgment and paranoia or psychosis at high doses 37 Tolerance to these effects develops over a period of days or weeks The amount of cannabis normally used for medicinal purposes is not believed to cause any permanent cognitive impairment in adults though long term treatment in adolescents should be weighed carefully as they are more susceptible to these impairments Withdrawal symptoms are rarely a problem with controlled medical administration of cannabinoids The ability to drive vehicles or to operate machinery may be impaired until a tolerance is developed 21 Although supporters of medical cannabis say that it is safe 36 further research is required to assess the long term safety of its use 23 38 Cognitive effects Further information long term effects of cannabis Recreational use of cannabis is associated with cognitive deficits especially for those who begin to use cannabis in adolescence As of 2021 update there is a lack of research into long term cognitive effects of medical use of cannabis but one 12 month observational study reported that MC patients demonstrated significant improvements on measures of executive function and clinical state over the course of 12 months 39 Impact on psychosis Exposure to THC can cause acute transient psychotic symptoms in healthy individuals and people with schizophrenia 14 A 2007 meta analysis concluded that cannabis use reduced the average age of onset of psychosis by 2 7 years relative to non cannabis use 40 A 2005 meta analysis concluded that adolescent use of cannabis increases the risk of psychosis and that the risk is dose related 41 A 2004 literature review on the subject concluded that cannabis use is associated with a two fold increase in the risk of psychosis but that cannabis use is neither necessary nor sufficient to cause psychosis 42 A French review from 2009 came to a conclusion that cannabis use particularly that before age 15 was a factor in the development of schizophrenic disorders 43 PharmacologyThe genus Cannabis contains two species which produce useful amounts of psychoactive cannabinoids Cannabis indica and Cannabis sativa which are listed as Schedule I medicinal plants in the US 4 a third species Cannabis ruderalis has few psychogenic properties 4 Cannabis contains more than 460 compounds 7 at least 80 of these are cannabinoids 44 45 chemical compounds that interact with cannabinoid receptors in the brain 4 As of 2012 more than 20 cannabinoids were being studied by the U S FDA 46 The most psychoactive cannabinoid found in the cannabis plant is tetrahydrocannabinol or delta 9 tetrahydrocannabinol commonly known as THC 7 Other cannabinoids include delta 8 tetrahydrocannabinol cannabidiol CBD cannabinol CBN cannabicyclol CBL cannabichromene CBC and cannabigerol CBG they have less psychotropic effects than THC but may play a role in the overall effect of cannabis 7 The most studied are THC CBD and CBN 47 CB1 and CB2 are the primary cannabinoid receptors responsible for several of the effects of cannabinoids although other receptors may play a role as well Both belong to a group of receptors called G protein coupled receptors GPCRs CB1 receptors are found in very high levels in the brain and are thought to be responsible for psychoactive effects 48 CB2 receptors are found peripherally throughout the body and are thought to modulate pain and inflammation 49 Absorption Cannabinoid absorption is dependent on its route of administration Inhaled and vaporized THC have similar absorption profiles to smoked THC with a bioavailability ranging from 10 to 35 Oral administration has the lowest bioavailability of approximately 6 variable absorption depending on the vehicle used and the longest time to peak plasma levels 2 to 6 hours compared to smoked or vaporized THC 50 Similar to THC CBD has poor oral bioavailability approximately 6 The low bioavailability is largely attributed to significant first pass metabolism in the liver and erratic absorption from the gastrointestinal tract However oral administration of CBD has a faster time to peak concentrations 2 hours than THC 50 Due to the poor bioavailability of oral preparations alternative routes of administration have been studied including sublingual and rectal These alternative formulations maximize bioavailability and reduce first pass metabolism Sublingual administration in rabbits yielded bioavailability of 16 and time to peak concentration of 4 hours 51 Rectal administration in monkeys doubled bioavailability to 13 5 and achieved peak blood concentrations within 1 to 8 hours after administration 52 Distribution Like cannabinoid absorption distribution is also dependent on route of administration Smoking and inhalation of vaporized cannabis have better absorption than do other routes of administration and therefore also have more predictable distribution 52 53 THC is highly protein bound once absorbed with only 3 found unbound in the plasma It distributes rapidly to highly vascularized organs such as the heart lungs liver spleen and kidneys as well as to various glands Low levels can be detected in the brain testes and unborn fetuses all of which are protected from systemic circulation via barriers 54 THC further distributes into fatty tissues a few days after administration due to its high lipophilicity and is found deposited in the spleen and fat after redistribution 53 55 56 Metabolism Delta 9 THC is the primary molecule responsible for the effects of cannabis Delta 9 THC is metabolized in the liver and turns into 11 OH THC 57 11 OH THC is the first metabolic product in this pathway Both Delta 9 THC and 11 OH THC are psychoactive The metabolism of THC into 11 OH THC plays a part in the heightened psychoactive effects of edible cannabis 58 Next 11 OH THC is metabolized in the liver into 11 COOH THC which is the second metabolic product of THC 59 11 COOH THC is not psychoactive 57 Ingestion of edible cannabis products lead to a slower onset of effect than the inhalation of it because the THC travels to the liver first through the blood before it travels to the rest of the body Inhaled cannabis can result in THC going directly to the brain where it then travels from the brain back to the liver in recirculation for metabolism 57 Eventually both routes of metabolism result in the metabolism of psychoactive THC to inactive 11 COOH THC Excretion Due to substantial metabolism of THC and CBD their metabolites are excreted mostly via feces rather than by urine 50 60 After delta 9 THC is hydroxylated into 11 OH THC via CYP2C9 CYP2C19 and CYP3A4 it undergoes phase II metabolism into more than 30 metabolites a majority of which are products of glucuronidation Approximately 65 of THC is excreted in feces and 25 in the urine while the remaining 10 is excreted by other means 50 The terminal half life of THC is 25 to 36 hours 61 whereas for CBD it is 18 to 32 hours 60 CBD is hydroxylated by P450 liver enzymes into 7 OH CBD Its metabolites are products of primarily CYP2C19 and CYP3A4 activity with potential activity of CYP1A1 CYP1A2 CYP2C9 and CYP2D6 62 Similar to delta 9 THC a majority of CBD is excreted in feces and some in the urine 50 The terminal half life is approximately 18 32 hours 63 Administration nbsp Illustrating various forms of medicinal cannabisSmoking has been the means of administration of cannabis for many users but it is not suitable for the use of cannabis as a medicine 64 It was the most common method of medical cannabis consumption in the US as of 2013 update 4 It is difficult to predict the pharmacological response to cannabis because concentration of cannabinoids varies widely as there are different ways of preparing it for consumption smoked applied as oils eaten infused into other foods or drunk and a lack of production controls 4 The potential for adverse effects from smoke inhalation makes smoking a less viable option than oral preparations 64 Cannabis vaporizers have gained popularity because of a perception among users that fewer harmful chemicals are ingested when components are inhaled via aerosol rather than smoke 4 Cannabinoid medicines are available in pill form dronabinol and nabilone and liquid extracts formulated into an oromucosal spray nabiximols 4 Oral preparations are problematic due to the uptake of cannabinoids into fatty tissue from which they are released slowly and the significant first pass liver metabolism which breaks down D9THC and contributes further to the variability of plasma concentrations 64 The US Food and Drug Administration FDA has not approved smoked cannabis for any condition or disease as it deems that evidence is lacking concerning safety and efficacy 65 The FDA issued a 2006 advisory against smoked medical cannabis stating marijuana has a high potential for abuse has no currently accepted medical use in treatment in the United States and has a lack of accepted safety for use under medical supervision 65 HistoryMain article History of medical cannabis Ancient Cannabis called ma 麻 meaning hemp cannabis numbness or dama 大麻 with big great in Chinese was used in Taiwan for fiber starting about 10 000 years ago 66 The botanist Hui lin Li wrote that in China The use of Cannabis in medicine was probably a very early development Since ancient humans used hemp seed as food it was quite natural for them to also discover the medicinal properties of the plant 67 Emperor Shen Nung who was also a pharmacologist wrote a book on treatment methods in 2737 BCE that included the medical benefits of cannabis He recommended the substance for many ailments including constipation gout rheumatism and absent mindedness 68 Cannabis is one of the 50 fundamental herbs in traditional Chinese medicine 69 The Ebers Papyrus c 1550 BCE from Ancient Egypt describes medical cannabis 70 The ancient Egyptians used hemp cannabis in suppositories for relieving the pain of hemorrhoids 71 Surviving texts from ancient India confirm that cannabis psychoactive properties were recognized and doctors used it for treating a variety of illnesses and ailments including insomnia headaches gastrointestinal disorders and pain including during childbirth 72 The Ancient Greeks used cannabis to dress wounds and sores on their horses 73 and in humans dried leaves of cannabis were used to treat nose bleeds and cannabis seeds were used to expel tapeworms 73 In the medieval Islamic world Arabic physicians made use of the diuretic antiemetic antiepileptic anti inflammatory analgesic and antipyretic properties of Cannabis sativa and used it extensively as medication from the 8th to 18th centuries 74 Landrace strains nbsp Evolution of cultivated cannabis strains The cultivar Cannabis ruderalis still grows wild today Cannabis seeds may have been used for food rituals or religious practices in ancient Europe and China 75 19 22 Harvesting the plant led to the spread of cannabis throughout Eurasia about 10 000 to 5 000 years ago with further distribution to the Middle East and Africa about 2 000 to 500 years ago 75 18 19 A landrace strain of cannabis developed over centuries 76 They are cultivars of the plant that originated in one specific region Widely cultivated strains of cannabis such as Afghani or Hindu Kush are indigenous to the Pakistan and Afghanistan regions while Durban Poison is native to Africa 75 45 48 There are approximately 16 landrace strains of cannabis identified from Pakistan Jamaica Africa Mexico Central America and Asia 77 Modern An Irish physician William Brooke O Shaughnessy is credited with introducing cannabis to Western medicine 78 O Shaughnessy discovered cannabis in the 1830s while living abroad in India where he conducted numerous experiments investigating the drug s medical utility noting in particular its analgesic and anticonvulsant effects 79 He returned to England with a supply of cannabis in 1842 after which its use spread through Europe and the United States 80 In 1845 French physician Jacques Joseph Moreau published a book about the use of cannabis in psychiatry 81 In 1850 cannabis was entered into the United States Pharmacopeia 79 An anecdotal report of Cannabis indica as a treatment for tetanus appeared in Scientific American in 1880 82 The use of cannabis in medicine began to decline by the end of the 19th century due to difficulty in controlling dosages and the rise in popularity of synthetic and opium derived drugs 80 Also the advent of the hypodermic syringe allowed these drugs to be injected for immediate effect in contrast to cannabis which is not water soluble and therefore cannot be injected 80 In the United States the medical use of cannabis further declined with the passage of the Marihuana Tax Act of 1937 which imposed new regulations and fees on physicians prescribing cannabis 83 Cannabis was removed from the U S Pharmacopeia in 1941 and officially banned for any use with the passage of the Controlled Substances Act of 1970 80 Cannabis began to attract renewed interest as medicine in the 1970s and 1980s in particular due to its use by cancer and AIDS patients who reported relief from the effects of chemotherapy and wasting syndrome 84 In 1996 California became the first U S state to legalize medical cannabis in defiance of federal law 85 In 2001 Canada became the first country to adopt a system regulating the medical use of cannabis 86 nbsp The use of cannabis at least as fiber has been shown to go back at least 10 000 years in Taiwan Da ma Pinyin pronunciation is the Chinese expression for cannabis the first character meaning big and the second character meaning hemp nbsp Cannabis indica fluid extract American Druggists Syndicate pre 1937 nbsp An advertisement for cannabis americana distributed by a pharmacist in New York in 1917 nbsp The Ebers Papyrus c 1550 BCE from Ancient Egypt has a prescription for medical marijuana applied directly for inflammation Society and cultureLegal status See also Legality of cannabis by country nbsp Legal status of whole plant medical cannabis worldwide Legal as authorized by a physician Legal for any use no prescription required See also countries that have decriminalized or where enforcement is limited Countries that have legalized the medical use of cannabis include Argentina 87 Australia 88 Brazil 89 Canada 90 Chile 90 Colombia 90 Costa Rica 91 Croatia 92 Cyprus 93 Czech Republic 90 Finland 94 Germany 95 Greece 96 Israel 97 Italy 98 Jamaica 99 Lebanon 100 Luxembourg 101 Malta 102 Morocco 103 the Netherlands 90 New Zealand 104 North Macedonia 105 Panama 106 Peru 107 Poland 108 Portugal 109 Rwanda 110 Spain 111 Sri Lanka 112 Switzerland 113 Thailand 114 the United Kingdom 115 and Uruguay 90 Other countries have more restrictive laws that allow only the use of isolated cannabinoid drugs such as Sativex or Epidiolex 116 117 Countries with the most relaxed policies include Canada 118 the Netherlands 90 Thailand 119 and Uruguay 90 where cannabis can be purchased without need for a prescription In Mexico THC content of medical cannabis is limited to one percent 120 In the United States the legality of medical cannabis varies by state 11 Cannabis and its derivatives are subject to regulation under three United Nations treaties the 1961 Single Convention on Narcotic Drugs the 1971 Convention on Psychotropic Substances and the 1988 Convention Against Illicit Traffic in Narcotic Drugs and Psychotropic Substances 121 Cannabis is classified as a Schedule I drug under the Single Convention treaty meaning that medical use is allowed but that it is considered to be an addictive drug with a serious risk of abuse along with other drugs such as opium and cocaine 122 Prior to December 2020 it was also included in Schedule IV a subset of Schedule I which is for only the most dangerous drugs such as heroin and fentanyl 123 Member nations of the UN Commission on Narcotic Drugs voted 27 25 to remove it from Schedule IV on 2 December 2020 124 following a World Health Organization recommendation for removal in January 2019 125 126 United States See also Medical cannabis in the United States In the United States the use of cannabis for medical purposes is legal in 38 states four out of five permanently inhabited U S territories and the District of Columbia 11 An additional 10 states have more restrictive laws allowing the use of low THC products 11 Cannabis remains illegal at the federal level under the Controlled Substances Act which classifies it as a Schedule I drug with a high potential for abuse and no accepted medical use In December 2014 however the Rohrabacher Farr amendment was signed into law prohibiting the Justice Department from prosecuting individuals acting in accordance with state medical cannabis laws 127 Economics Distribution nbsp Medical marijuana dispensary in Denver ColoradoThe method of obtaining medical cannabis varies by region and by legislation In the US most consumers grow their own or buy it from cannabis dispensaries in states where it is legal 4 128 Marijuana vending machines for selling or dispensing cannabis are in use in the United States and are planned to be used in Canada 129 In 2014 the startup Meadow began offering on demand delivery of medical marijuana in the San Francisco Bay Area through their mobile app 130 Almost 70 of medical cannabis is exported from the United Kingdom according to a 2017 United Nations report with much of the remaining amount coming from Canada and the Netherlands 131 Insurance In the United States health insurance companies may not pay for a medical marijuana prescription as the Food and Drug Administration must approve any substance for medicinal purposes Before this can happen the FDA must first permit the study of the medical benefits and drawbacks of the substance which it has not done since it was placed on Schedule I of the Controlled Substances Act in 1970 Therefore all expenses incurred fulfilling a medical marijuana prescription will possibly be incurred as out of pocket 132 However the New Mexico Court of Appeals has ruled that workers compensation insurance must pay for prescribed marijuana as part of the state s Medical Cannabis Program 133 Positions of medical organizations Medical organizations that have issued statements in support of allowing access to medical cannabis include the American Nurses Association 8 American Public Health Association 134 American Medical Student Association 135 National Multiple Sclerosis Society 136 Epilepsy Foundation 137 and Leukemia amp Lymphoma Society 138 Organizations that oppose the legalization of medical cannabis include the American Academy of Pediatrics 10 and American Psychiatric Association 139 However the AAP also supports rescheduling for the purpose of facilitating research 10 The American Medical Association 140 and American College of Physicians 141 do not take a position on the legalization of medical cannabis but have called for the Schedule I classification to be reviewed The American Academy of Family Physicians 9 and American Society of Addiction Medicine 142 also do not take a position but do support rescheduling to better facilitate research The American Heart Association says that many of the concerning health implications of cannabis include cardiovascular diseases but that it supports rescheduling to allow more nuanced marijuana legislation and regulation and to reflect the existing science behind cannabis 143 The American Cancer Society 144 and American Psychological Association 145 have noted the obstacles that exist for conducting research on cannabis and have called on the federal government to better enable scientific study of the drug Cancer Research UK say that while cannabis is being studied for therapeutic potential claims that there is solid proof that cannabis or cannabinoids can cure cancer is highly misleading to patients and their families and builds a false picture of the state of progress in this area 146 Brand names In the US the FDA has approved two oral cannabinoids for use as medicine dronabinol and nabilone 4 Dronabinol synthetic THC is listed as Schedule II 147 Nabilone a synthetic cannabinoid is also Schedule II indicating high potential for side effects and addiction 46 Both received approval for sale in the US in 1985 under the brand names Marinol and Cesamet 148 Nabiximols an oromucosal spray derived from two strains of Cannabis sativa and containing THC and CBD 46 is not approved in the United States but is approved in several European countries Canada and New Zealand as of 2013 4 As of 2018 medical marijuana in Canada is being legally distributed to registered patients in bud drops and capsule forms by such companies as Canopy Growth Corp and Aurora Cannabis Genericmedication Brand name s Country Licensed indicationsNabilone Cesamet U S Canada Antiemetic treatment of nausea or vomiting associated with chemotherapy that has failed to respond adequately to conventional therapy 4 Dronabinol MarinolSyndros U S Anorexia associated with AIDS related weight loss 4 Nabiximols Sativex Canada New Zealand majority of the EU 149 Limited treatment for spasticity and neuropathic pain associated with multiple sclerosis and intractable cancer pain 4 As an antiemetic these medications are usually used when conventional treatment for nausea and vomiting associated with cancer chemotherapy fail to work 4 Nabiximols is used for treatment of spasticity associated with MS when other therapies have not worked and when an initial trial demonstrates meaningful improvement 4 Trials for FDA approval in the US are underway 4 It is also approved in several European countries for overactive bladder and vomiting 46 When sold under the trade name Sativex as a mouth spray the prescribed daily dose in Sweden delivers a maximum of 32 4 mg of THC and 30 mg of CBD mild to moderate dizziness is common during the first few weeks 150 Relative to inhaled consumption peak concentration of oral THC is delayed and it may be difficult to determine optimal dosage because of variability in patient absorption 4 In 1964 Albert Lockhart and Manley West began studying the health effects of traditional cannabis use in Jamaican communities They developed and in 1987 gained permission to market the pharmaceutical Canasol one of the first cannabis extracts 151 ResearchMain article Medical cannabis research Medical cannabis research includes any medical research on using cannabis as a treatment for any medical condition For reasons including increased popular support of cannabis use a trend of cannabis legalization and the perception of medical 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Cannabis Research of the University of California Medical Marijuana a 2014 2015 three part CNN documentary produced by Sanjay Gupta Marijuana and Medical Marijuana collected news and commentary at The New York Times Retrieved from https en wikipedia org w index php title Medical cannabis amp oldid 1207034203, wikipedia, wiki, book, books, library,

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