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Mitragyna speciosa

From Wikipedia, the free encyclopedia
Mitragyna speciosa
Mitragyna speciosa111.JPG
Scientific classification e
Kingdom: Plantae
Clade: Angiosperms
Clade: Eudicots
Clade: Asterids
Order: Gentianales
Family: Rubiaceae
Genus: Mitragyna
Species: M. speciosa
Binomial name
Mitragyna speciosa
(Korth.) Havil.
  • Nauclea korthalsii Steud. nom. inval.
  • Nauclea luzoniensis Blanco
  • Nauclea speciosa (Korth.) Miq.
  • Stephegyne speciosa Korth.

Mitragyna speciosa (commonly known as kratom[2] also ketum) is a tropical evergreen tree in the coffee family native to Southeast Asia. M. speciosa is indigenous to Thailand, Indonesia, Malaysia, Myanmar, and Papua New Guinea,[3] where it has been used in traditional medicine since at least the 19th century.[4] Kratom has opioid properties and some stimulant-like properties.[5][6][7]

As of 2018, little is known of kratom's worth or safety as a therapeutic agent, since research into its use has been of poor quality.[8][9] In February 2018, the FDA stated that there is no evidence kratom is safe or effective for treating any condition.[6] Some people take it for managing chronic pain, for treating opioid withdrawal symptoms, or – more recently – for recreational purposes.[3][9] Onset of effects typically begins within 5 to 10 minutes and lasts 2 to 5 hours.[3]

Common minor side effects may include nausea, vomiting, and constipation.[3] More severe side effects may include respiratory depression (decreased breathing), seizure, addiction, and psychosis.[3][6][10][11] Other side effects may include high heart rate and blood pressure, trouble sleeping, and, rarely, liver toxicity.[3][12][13] When use is stopped, withdrawal may occur.[7][9] Deaths have occurred with kratom both by itself and mixed with other substances.[6][14] There were 44 kratom-related deaths in the United States between 2011 and 2017,[6] and nine in Sweden over 2011 to 2012.[14]

As of 2018, there is growing international concern about a possible threat to public health from kratom use.[6][9][15] In some jurisdictions, its sale and importation have been restricted, and a number of public health authorities have raised alerts.[9][15][16] Kratom is a controlled substance in 16 countries,[6] and in 2014, the United States Food and Drug Administration (FDA) banned imports and manufacturing of kratom as a dietary supplement.[17] Sometimes, the finished product is mixed into cocktails with other psychoactive drugs such as caffeine and codeine.[7][18]


Young M. speciosa tree

Mitragyna speciosa is an evergreen tree that can grow to a height of 25 m (82 ft) tall and the trunk may grow to a 0.9 m (3 ft) diameter.[19] The trunk is generally straight and the outer bark is smooth and grey.[19] The leaves are dark green and glossy,[9] and can grow to over 14–20 cm (5.5–7.9 in) long and 7–12 cm (2.8–4.7 in) wide when fully open, are ovate-acuminate in shape, and opposite in growth pattern, with 12–17 pairs of veins.[19] The flowers grow in clusters of three at the ends of the branches. The calyx-tube is 2 mm (0.079 in) long and has 5 lobes; the corolla-tube is 2.5–3 millimetres (0.098–0.118 in) long.[19]

M. speciosa is indigenous to Thailand, Indonesia, Malaysia, Myanmar, and Papua New Guinea.[3]

Mitragyna speciosa was first formally described by the Dutch colonial botanist Pieter Korthals in 1839, who named it as such; it was renamed and reclassified several times before George Darby Haviland provided the final name and classification in 1859.[19]:59


The United States Drug Enforcement Administration stated in 2013: "There is no legitimate medical use for kratom".[10] Kratom has become popular as a recreational drug and has been promoted with claims that it can improve mood, relieve pain and help with opiate addiction.[16] As of 2013, kratom and key extracts have been studied in cells and in animals, but no clinical trials have been conducted in the United States.[4]

Opioid withdrawal

In 1836, kratom was reported to be used as an opium substitute in Malaysia. Kratom was also used as an opium substitute in Thailand in the 19th century.[4]

Data on how often it is used worldwide are lacking as it is not detected by typical drug screening tests.[20] Rates of kratom use appears to be increasing among those who have been self-managing chronic pain with opioids purchased without a prescription and are cycling (but not quitting) their use.[20] As of 2018, there have been no formal trials to study the efficacy or safety of kratom to treat opioid addiction.[6]

Traditional use

Kratom leaves

In cultures where the plant grows, it has been used in traditional medicine. The leaves are chewed to relieve musculoskeletal pain and increase energy, appetite, and sexual desire in ways similar to khat and coca.[9] The leaves or extracts from them are used to heal wounds and as a local anesthetic. Extracts and leaves have been used to treat coughs, diarrhea, and intestinal infections.[3][4][19] Kratom is often used by workers in laborious or monotonous professions to stave off exhaustion as well as a mood enhancer and/or painkiller.[19] In Thailand, kratom was "used as a snack to receive guests and was part of the ritual worship of ancestors and gods."[21] The herb is very bitter and is generally combined with a sweetener.[20]

Recreational use

Across Southeast Asia, and especially in Thailand in the 2010s, a tea-based cocktail known as 4×100 became popular among some younger people. It is a mix of kratom leaves, cough syrup, Coca-Cola, and ice; as of 2011, people who consumed this were often viewed more negatively than users of traditional kratom, but not as negatively as users of heroin.[22] As of 2012, use of the cocktail was a severe problem among youth in three provinces along the border with Malaysia.[23]

In the US, as of 2015, kratom was available in head shops and over the internet; prevalence of use was unknown as of that time.[9]

Adverse effects

At relatively low doses (1–5 g of raw leaves) at which there are mostly stimulant effects, side effects include contracted pupils and blushing; adverse effects related to stimulation include anxiety and agitation, and opioid-related effects like itching, nausea, loss of appetite, and increased urination begin to appear.[3][9] At moderate (5 to 15 g of raw leaves) doses and higher, at which opioid effects generally appear, additional adverse effects include tachycardia (increased stimulant effect) as well as the opioid side effects of constipation, dizziness, hypotension, dry mouth, and sweating.[9][11] Frequent use of high doses of kratom may cause tremor, anorexia, weight loss, seizures, and psychosis.[9] If heavy users try to stop using kratom, they may experience withdrawal symptoms including irritability, feelings of distress, nausea, hypertension, insomnia, runny nose, muscle and joint pain, and diarrhea.[9][7]

Serious toxicity is relatively rare and generally appears at high doses or when kratom is used with other substances.[3][9]

In July 2016, the Centers for Disease Control (CDC) issued a report stating that between 2010 and 2015, US Poison Centers received 660 reports of exposure to kratom. Medical outcomes associated with kratom exposure were reported as minor (minimal signs or symptoms, which resolved rapidly with no residual disability) for 162 (24.5%) exposures, moderate (non-life-threatening, with no residual disability, but requiring some form of treatment) for 275 (41.7%) exposures, and major (life-threatening signs or symptoms, with some residual disability) for 49 (7.4%) exposures.[13] One death was reported in a person who was exposed to the medications paroxetine (an antidepressant) and lamotrigine (an anticonvulsant and mood stabilizer) in addition to kratom. For 173 (26.2%) exposure calls, no effects were reported, or poison center staff members were unable to follow up again regarding effects.[13]

Overdose of kratom is managed similar to opioid overdose, and naloxone can be considered to treat an overdose that results in a reduced impulse to breathe, despite mixed results for its utility, based on animal models.[3]

Respiratory depression

Respiratory depression is a major risk with opioids, especially those that have activity at the mu-opioid receptor. This is the leading cause of death from opioid use.[24]:196 In animal studies at very high doses, mitragynine caused respiratory depression, but less than morphine or codeine.[24]:196[20] The respiratory effects of kratom and its main bioactive components have not been studied in people.[4][24]:196

A 2016 CDC report on kratom exposures did not list respiratory depression as a risk of kratom,[13] nor did a 2013 DEA report.[10] The Food and Drug Administration in a July 2016 report does however list respiratory depression as one of the concerns.[25] Some literature review articles do not list respiratory depression;[4][9] however other literature reviews and some medical textbooks do name respiratory depression as a risk.[3][26][11][27]:15

Liver toxicity

In rare cases, chronic use of kratom has been linked to acute liver injury with associated symptoms of fatigue, nausea, itching and jaundice.[12][28] Liver injury is associated with cholestasis and may involve acute renal failure.[12] As of 2016, the mechanism by which kratom causes liver damage in some people was poorly understood.[28]


Kratom overdose is a subject of concern in many countries because of the rising number of hospitalizations and deaths from chronic kratom abuse.[5][9][12] According to clinical reviews, kratom overdose can cause liver toxicity, seizures, coma and death,[12] especially when in combination with alcohol abuse.[5] Between 2011 and 2017, forty four deaths in the United States were kratom-related.[6] In one autopsy, substantial levels of mitragynine and the psychostimulant, propylhexedrine, were found in the blood sample.[14] In an additional autopsy were high levels of mitragynine and signs of opioid toxicity.[9] Nine deaths occurred in Sweden during 2010-11 relating to use of Krypton, a kratom mixture with O-desmethyltramadol.[14][26]


The key psychoactive compounds in M. speciosa are mitragynine and 7-hydroxymitragynine (7-HMG),[9] but there are more than 40 compounds in M. speciosa leaves,[20] including about 25 alkaloids other than mitragynine and 7-hydroxymitragynine including ajmalicine, mitraphylline, mitragynine pseudoindoxyl, and Rhynchophylline.[29][30] Other active chemicals in M. speciosa include raubasine (best known from Rauvolfia serpentina) and Pausinystalia johimbe alkaloids such as corynantheidine.[31]

Mitragynine is about 60% of alkaloid extractions, while 7-hydroxymitragynine is about 2%.[9] Mitragynine is structurally similar to yohimbine and voacangine.[9]


As of 2017, much of the pharmacology of kratom was not well understood, having stimulant effects at low doses, an opioid-like effect at higher doses, as well as sedative and sensory-suppressive effects.[5][8][9]

Both mitragynine and 7-HMG are selective full agonists of the μ-opioid receptor; 7-HMG appears to have higher affinity.[9] The stimulant effects appear to be mediated via prevention of activation of serotonin 5-HT2A receptors and postsynaptic α2-adrenergic receptors.[9] Rhynchophylline is a non-competitive NMDA antagonist found in kratom.[9]

Mitragynine is metabolized in humans via phase I and phase II mechanisms with the resulting metabolites excreted in urine.[9] In in vitro experiments, kratom extracts inhibited CYP3A4, CYP2D6, and CYP1A2 enzymes, which results in significant potential for drug interactions.[9]

Detection in body fluids

The plant's active compounds and metabolites are not detected by a typical drug screening test, but can be detected by more specialized testing.[32][26] Blood mitragynine concentrations are expected to be in a range of 10–50 μg/L in persons using the drug recreationally. Detection in body fluids is typically by liquid chromatography-mass spectrometry.[26][33]


As of January 2018, neither the plant nor its alkaloids were listed in any of the Schedules of the United Nations Drug Conventions.[15]


As of 2013, kratom was listed by ASEAN in its annex of products that cannot be included in traditional medicines and health supplements that are traded across ASEAN nations.[34]

Australia and New Zealand

As of January 2015, kratom was controlled as a narcotic in Australia and under Medicines Regulations 1985 (Amended August 6, 2015)[35] of New Zealand.[15]


As of October 2016, it was not legal to market kratom for any use in which it was ingested, but could be marketed for other uses, such as incense.[36] Health Canada has taken action against companies marketing it for ingestion.[37][38]


In Europe, as of 2011, the plant was controlled in Denmark, Latvia, Lithuania, Poland, Romania and Sweden.[15] In the UK, since 2016, the sale, import, and export of kratom are prohibited under the Psychoactive Substances Act.[39]


The use of kratom leaves, known locally as 'ketum', is prohibited in Malaysia under Section 30 (3) Poisons Act 1952 and the user may be fined with a maximum amount of MYR 10,000 (USD 3,150) or up to 4 years imprisonment.[40] Certain parties have urged the government to penalize the use of kratom under the Dangerous Drugs Act instead of the Poisons Act, which will carry heavier penalties.[41]


Possession of kratom leaves is illegal in Thailand. The Thai government passed the Kratom Act 2486, effective August 3, 1943, which made planting the tree illegal,[10] in response to a rise in its use when opium became very expensive in Thailand and the Thai government was attempting to gain control in the opium market.[9] In 1979, the Thai government placed kratom, along with marijuana, in Category V of a five category classification of narcotics.[10] Kratom accounted for less than 2% of arrests for narcotics between 1987 and 1992.[42]

The government considered legalizing kratom in 2004, 2009, and 2013.[43]

United States

The FDA coordinated with other US agencies to seize shipments of imported kratom in 2014, as the product was being marketed as a dietary supplement, but had never been commonly used in the United States or to be confirmed as safe.[17][44]

On 30 August 2016, the Drug Enforcement Administration (DEA) announced its intention to place the active materials in the kratom plant into Schedule I of the Controlled Substances Act as a warning about an imminent hazard to public safety, citing over 600 calls to poison control centers between 2010 and 2015 and 15 kratom-related deaths between 2014 and 2016.[16] This drew strong protests among those using kratom to deal with chronic pain or wean themselves off opioids or alcohol.[45] A group of 51 members of the US House of Representatives and a group of 9 senators each sent letters to Acting DEA Administrator Chuck Rosenberg protesting the listing and around 140,000 people signed an online White House Petition protesting it.[46][47] The DEA noted the responses but said that it intended to go forward with the listing; a spokesman said: "We can't rely upon public opinion and anecdotal evidence. We have to rely upon science."[48] In October 2016, the DEA withdrew its notice of intent while inviting public comments over a review period ending 1 December 2016.[49][50]

As of May 2016, Alabama, Arkansas, Indiana, Tennessee, Vermont, and Wisconsin had made kratom illegal,[51] and the US Army had forbidden soldiers from using it.[52]

In November 2017, the FDA cited serious concerns over the marketing and effects (including death) associated with the use of kratom in the United States, stating that "There is no reliable evidence to support the use of kratom as a treatment for opioid use disorder; there are currently no FDA-approved therapeutic uses of kratom... and the FDA has evidence to show that there are significant safety issues associated with its use."[53] In February 2018, the Commissioner of the FDA, Scott Gottlieb, released a statement describing further opioid-like properties of kratom and that it should not be used for any medical treatment or recreational use.[6]

See also


  1. ^ Mitragyna speciosa (Korth.) Havil. is an accepted name . Retrieved 2013-12-26.
  2. ^ "Mitragyna speciosa". Germplasm Resources Information Network (GRIN). Agricultural Research Service (ARS), United States Department of Agriculture (USDA). Retrieved 2013-12-26. 
  3. ^ a b c d e f g h i j k l Rech, MA; Donahey, E; Cappiello Dziedzic, JM; Oh, L; Greenhalgh, E (February 2015). "New drugs of abuse". Pharmacotherapy. 35 (2): 189–97. doi:10.1002/phar.1522. PMID 25471045. 
  4. ^ a b c d e f Hassan, Z; Muzaimi, M; Navaratnam, V; Yusoff, N. H; Suhaimi, F. W; Vadivelu, R; Vicknasingam, B. K; Amato, D; von Hörsten, S; Ismail, N. I; Jayabalan, N; Hazim, A. I; Mansor, S. M; Müller, C. P (2013). "From Kratom to mitragynine and its derivatives: Physiological and behavioural effects related to use, abuse, and addiction". Neuroscience & Biobehavioral Reviews. 37 (2): 138–51. doi:10.1016/j.neubiorev.2012.11.012. PMID 23206666. 
  5. ^ a b c d Fluyau, D; Revadigar, N (2017). "Biochemical Benefits, Diagnosis, and Clinical Risks Evaluation of Kratom". Frontiers in Psychiatry. 8: 62. doi:10.3389/fpsyt.2017.00062. PMC 5402527Freely accessible. PMID 28484399. 
  6. ^ a b c d e f g h i j Gottlieb, Scott (6 February 2018). "Statement from FDA Commissioner Scott Gottlieb, M.D., on the agency's scientific evidence on the presence of opioid compounds in kratom, underscoring its potential for abuse". US Food and Drug Administration. Retrieved 6 February 2018. 
  7. ^ a b c d Cinosi, E; Martinotti, G; Simonato, P; Singh, D; Demetrovics, Z; Roman-Urrestarazu, A; Bersani, F. S; Vicknasingam, B; Piazzon, G; Li, J. H; Yu, W. J; Kapitány-Fövény, M; Farkas, J; Di Giannantonio, M; Corazza, O (2015). "Following "the Roots" of Kratom (Mitragyna speciosa): The Evolution of an Enhancer from a Traditional Use to Increase Work and Productivity in Southeast Asia to a Recreational Psychoactive Drug in Western Countries". BioMed Research International. 2015: 968786. doi:10.1155/2015/968786. PMC 4657101Freely accessible. 
  8. ^ a b White CM (2017). "Pharmacologic and clinical assessment of kratom". Am J Health Syst Pharm (Review). doi:10.2146/ajhp161035. PMID 29255059. 
  9. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z Warner ML, Kaufman NC, Grundmann O (2016). "The pharmacology and toxicology of kratom: from traditional herb to drug of abuse". Int. J. Legal Med. (Review). 130 (1): 127–38. doi:10.1007/s00414-015-1279-y. PMID 26511390. 
  10. ^ a b c d e "KRATOM (Mitragyna speciosa korth)" (PDF). U.S. Drug Enforcement Administration. January 2013. Archived from the original (PDF) on 11 June 2016. 
  11. ^ a b c Marx, John; Walls, Ron; Hockberger, Robert (2014). "Chapter 156: Hallucinogens". Rosen's emergency medicine : concepts and clinical practice (Eighth ed.). London: Elsevier Health Sciences. pp. 2015–23. ISBN 9781455749874. 
  12. ^ a b c d e "Kratom". LiverTox, National Library of Medicine, US National Institutes of Health. 9 March 2017. Retrieved 29 March 2017. 
  13. ^ a b c d Anwar, Mehruba; Law, Royal; Schier, Josh (2016-01-01). "Notes from the Field: Kratom (Mitragyna speciosa) Exposures Reported to Poison Centers – United States, 2010–2015". MMWR. Morbidity and Mortality Weekly Report. 65 (29): 748–49. doi:10.15585/mmwr.mm6529a4. ISSN 0149-2195. PMID 27466822. 
  14. ^ a b c d "Mitragynine". Toxnet, National Library of Medicine, US National Institutes of Health. 14 February 2012. Retrieved 15 February 2018. 
  15. ^ a b c d e "Kratom profile (chemistry, effects, other names, origin, mode of use, other names, medical use, control status)". Page last updated 8 January 2015: European Monitoring Centre for Drugs and Drug Addiction. Retrieved 12 September 2016. 
  16. ^ a b c "DEA Announces Intent to Schedule Kratom: SE Asian drug is imminent hazard to public safety". US Drug Enforcement Administration. 30 August 2016. Archived from the original on 15 September 2016. Retrieved 31 August 2016. 
  17. ^ a b "Import Alert 54-15; Detention without physical examination of dietary supplements and bulk dietary ingredients that are or contain Mitragyna speciosa or kratom". U.S. Food and Drug Administration. 28 February 2014. Retrieved 18 April 2014. 
  18. ^ Karch, Steven B.; Drummer, Olaf (2015). Karch's Pathology of Drug Abuse (Fifth ed.). CRC Press. p. 528. ISBN 9781439861479. 
  19. ^ a b c d e f g Eisenman, Sasha W (2014). "Chapter 5. The Botany of Mitragyna speciosa (Korth.) Havil. and Related Species". In Raffa, Robert B. Kratom and Other Mitragynines: The Chemistry and Pharmacology of Opioids from a Non-Opium. CRC Press. pp. 57–76. ISBN 978-1-4822-2519-8. 
  20. ^ a b c d e Adkins, Jessica E.; Edward W. Boyer; Christopher R. McCurdy (2011-05-01). "Mitragyna speciosa, a psychoactive tree from Southeast Asia with opioid activity". Current Topics in Medicinal Chemistry. 11 (9): 1165–75. doi:10.2174/156802611795371305. PMID 21050173. 
  21. ^ Singh, Darshan; Narayanan, Suresh; Vicknasingam, Balasingam (September 2016). "Traditional and non-traditional uses of Mitragynine (Kratom): A survey of the literature". Brain Research Bulletin. 126 (Pt 1): 41–46. doi:10.1016/j.brainresbull.2016.05.004. PMID 27178014. 
  22. ^ Tanguay, Pascal (April 2011). "Kratom in Thailand: Decriminalisation and Community Control?" (PDF). Transnational Institiute. Young people feel the need to drink 4x100 in hidden settings due to fears of arrest by law enforcement. In one district, 21 of 39 villages reported the presence of 4x100 users in their community. Compared to traditional use, 4x100 users are subject to some measure of community discrimination, though community perceptions are far milder than for yaba or heroin users. 
  23. ^ Fuller, Thomas (23 July 2012). "A Fading Thai Drug Finds Its Resurgence in a Cocktail". The New York Times. 
  24. ^ a b c Jaclyn R. Beckett (2014). "Non-Analgesic CNS Effects". In Raffa, Robert B. Kratom and other mitragynines : the chemistry & pharmacology of opioids from. CRC Press. pp. 195–204. ISBN 9781482225181. 
  25. ^ "Import Alert 54-15". FDA. 25 July 2016. Retrieved 4 October 2016. 
  26. ^ a b c d Rosenbaum CD, Carreiro SP, Babu KM (2012). "Here today, gone tomorrow…and back again? A review of herbal marijuana alternatives (K2, Spice), synthetic cathinones (bath salts), kratom, Salvia divinorum, methoxetamine, and piperazines". Journal of Medical Toxicology. 8 (1): 15–32. doi:10.1007/s13181-011-0202-2. PMC 3550220Freely accessible. PMID 22271566. 
  27. ^ Nelson, Michael E.; Bryant, Sean M.; Aks, Steven E. (2014). "Emerging Drugs of Abuse". In Smith, Silas W.; Lugassy, Daniel M. Clinical Toxicology, An Issue of Emergency Medicine Clinics of North America, Volume 32, Issue 1 of The Clinics: Internal Medicine. Elsevier Health Sciences. pp. 1–28. ISBN 9780323266550. 
  28. ^ a b Pantano, F; Tittarelli, R; Mannocchi, G; Zaami, S; Ricci, S; Giorgetti, R; Terranova, D; Busardò, FP; Marinelli, E (16 April 2016). "Hepatotoxicity Induced by "the 3Ks": Kava, Kratom and Khat". International journal of molecular sciences. 17 (4): 580. doi:10.3390/ijms17040580. PMC 4849036Freely accessible. PMID 27092496. 
  29. ^ Suhaimi FW, Yusoff NH, Hassan R, Mansor SM, Navaratnam V, Müller CP, Hassan Z (2016). "Neurobiology of Kratom and its main alkaloid mitragynine". Brain Res Bull. Mar 25 (Pt 1): 29–40. doi:10.1016/j.brainresbull.2016.03.015. PMID 27018165. 
  30. ^ Prozialeck, WC; Jivan, JK; Andurkar, SV (2012). "Pharmacology of kratom: an emerging botanical agent with stimulant, analgesic, and opioid-like effects". The Journal of the American Osteopathic Association. 112 (12): 792–99. PMID 23212430. 
  31. ^ Takayama, Hiromitsu; et al. (2002). "Studies on the Synthesis and Opioid Agonistic Activities of Mitragynine-Related Indole Alkaloids: Discovery of Opioid Agonists Structurally Different from Other Opioid Ligands". Journal of Medicinal Chemistry. 45 (9): 1949–56. doi:10.1021/jm010576e. PMID 11960505. 
  32. ^ Le D, Goggin MM, Janis GC (2012). "Analysis of mitragynine and metabolites in human urine for detecting the use of the psychoactive plant kratom". Journal of Analytical Toxicology. 36 (9): 616–25. doi:10.1093/jat/bks073. PMID 23024321. 
  33. ^ Baselt RC (2014). Disposition of toxic drugs and chemicals in man. Seal Beach, Calif.: Biomedical Publications. p. 1382. ISBN 978-0-9626523-9-4. 
  34. ^ "Annex I: ASEAN Guiding Principles For Inclusion into or Exclusion from the Negative List of Substances for Traditional Medicines and Health Supplements" (PDF). Association of South East Asian Nations (ASEAN). June 28, 2014. Retrieved September 12, 2016. 
  35. ^ "Medicines Regulations 1984". New Zealand Legislation. Retrieved 31 May 2017. 
  36. ^ Coles, Terri (14 October 2016). "After U.S. delayed decision on kratom, a look at Canada's laws on the psychadelic plant". Yahoo News Canada. 
  37. ^ "Health Product Advertising Complaints". Health Canada, Health Products and Food Branch. Archived from the original on 14 February 2017. 
  38. ^ Kratom, a controversial herbal product, seized from 2 Edmonton stores: Health Canada
  39. ^ "Psychoactive Substances Act 2016". 
  40. ^ "Amend the Act leaves the density of the Dangerous Drugs Act". 13 December 2012. Retrieved 18 April 2014. 
  41. ^ Pengasih wants abuse of kratom leaves penalised under Dangerous Drugs Act. The Malaysian Insider. October 28, 2012.
  42. ^ Cheurprakobkit, Sutham (2000). "The drug situation in Thailand: the role of government and the police". Drug and Alcohol Review. 19 (1): 17–26. doi:10.1080/09595230096101. 
  43. ^ Prasert, Poungchompoo (October 4, 2013). "Decision yet to be reached on making 'kratom' legal". The Nation (Thailand). 
  44. ^ "Product Seizure Shows FDA Serious about Kratom". Natural Products Insider. 9 January 2016. 
  45. ^ Silverman, Lauren (12 September 2016). "Kratom Advocates Speak Out Against Proposed Government Ban". NPR. Retrieved 12 September 2016. 
  46. ^ Ingraham, Christopher (September 30, 2016). "DEA defies senators' appeal to reconsider 'unprecedented' kratom ban". Washington Post. 
  47. ^ Stapleton, Christine (September 29, 2016). "Congress members ask DEA not to ban kratom: opiod research needed". Palm Beach Post. 
  48. ^ Nelson, Steven (September 30, 2016). "Kratom Will Remain Legal for Days, Possibly Longer". US News & World Report. 
  49. ^ "Kratom Gets Reprieve From Drug Enforcement Administration". Retrieved 2016-10-12. 
  50. ^ "Withdrawal of Notice of Intent to Temporarily Place Mitragynine and 7-Hydroxymitragynine Into Schedule I: A Proposed Rule by the Drug Enforcement Administration on 10/13/2016". Federal Register. Drug Enforcement Administration. 2016-10-13. Retrieved 2016-10-18. 
  51. ^ Brown, Melissa (May 20, 2016). "States ban kratom supplement over abuse worries". Associated Press via US News & World Report. 
  52. ^ Schwarz, Alan (2 January 2016). "Kratom, an Addict's Alternative, Is Found to Be Addictive Itself". The New York Times. 
  53. ^ "Statement from FDA Commissioner Scott Gottlieb, M.D. on FDA advisory about deadly risks associated with kratom". U.S. Food and Drug Administration. 14 November 2017. Retrieved 14 November 2017. Patients addicted to opioids are using kratom without dependable instructions for use and more importantly, without consultation with a licensed health care provider about the product’s dangers, potential side effects or interactions with other drugs. There’s clear data on the increasing harms associated with kratom. Calls to U.S. poison control centers regarding kratom have increased 10-fold from 2010 to 2015, with hundreds of calls made each year. The FDA is aware of reports of 36 deaths associated with the use of kratom-containing products. There have been reports of kratom being laced with other opioids like hydrocodone. The use of kratom is also associated with serious side effects like seizures, liver damage and withdrawal symptoms 

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