Kratom

Purported Benefits, Side Effects & More

Kratom

Purported Benefits, Side Effects & More
Share
Share
Kratom

Common Names

  • Kratom; Cratom
  • Ketum; Kakuam
  • Biak
  • Mitragyne; Mitragyna; Mitragynine
  • Thang; Thom

For Patients & Caregivers

Tell your healthcare providers about any dietary supplements you’re taking, such as herbs, vitamins, minerals, and natural or home remedies. This will help them manage your care and keep you safe.


What is it?

Kratom is an herbal supplement that has properties similar to other opioids. It is not recommended as a treatment for pain at this time due to lack of research, harmful side effects, and product contamination.

Kratom is an herbal supplement known to have both stimulant and calming effects. It may also have pain-relieving properties similar to opioids. However, kratom cannot be used as a substitution for prescription pain medications, because studies on its safety or usefulness in humans have not been conducted. Its use is banned in some countries and US states due to potential for abuse. Moreover, some kratom products were recalled due to contamination.

What are the potential uses and benefits?

In general there are very limited data on effects in humans for all uses. More research is needed to determine the safety and effectiveness of this herbal supplement.

Anxiety

Although animal studies suggest kratom may relieve anxiety, it may also cause anxiety in humans during withdrawal.

Insomnia

Kratom appears to have sedative effects at higher doses.

Pain relief

Kratom appears to have pain-relieving effects at higher doses.

Stimulant

Lower doses of kratom have been traditionally used for its stimulating effects. It may also cause appetite suppression.

What are the side effects?

Withdrawal symptoms: Flu-like symptoms such as nausea, vomiting, chills, sweats, muscle spasms and pain, decreased appetite, or diarrhea; anxiety, irritability, depressed mood, hot flashes, sleeping difficulty. Symptoms are more likely with heavier use.

Case reports

Numerous adverse effects involving the use of kratom and mitragynine have been reported in the medical literature across the following categories:

  • Addiction, withdrawal symptoms
  • Depression/anxiety relapse
  • Heart and lung problems
  • Kidney and liver injury
  • Multiorgan dysfunction/failure
  • Psychosis, seizures
  • Tissue damage
  • Temporary paralysis
  • Overdose, death
What else do I need to know?

Patient Warnings:

  • The FDA recently recalled powdered kratom supplements for salmonella contamination and issued a public health advisory against kratom. It also issued warnings of addiction and overdose risks similar to that of other opioids.
  • The Drug Enforcement Administration includes kratom on its Drugs of Concern list. These substances are not currently regulated by the Controlled Substances Act, but pose risks to persons who abuse them. In addition, the National Institute of Drug Abuse identified kratom as an emerging drug of abuse.

Do Not Take if:

  • You have heart problems: Lab studies and case reports suggest kratom could worsen heart problems.
  • You are taking CYP450 or UGT substrate drugs: Kratom may affect the clearance of these drugs.
  • You are taking P-glycoprotein substrate drugs: When taken with psychoactive drugs that are P-gp substrates, mitragynine may cause significant toxicity.

Special Point:

  • Several countries and US states have banned kratom.

For Healthcare Professionals

Scientific Name
Mitragyna speciosa
Clinical Summary

Mitragyna speciosa, commonly known as kratom, is indigenous to Southeast Asia. The leaves have been used in traditional medicine to treat pain, fatigue, fever, diarrhea, and wounds (1), while its extracts are known for their psychoactive properties, especially morphine-like effects (2). Kratom has gained popularity as a supplement to improve mood, and decrease anxiety and pain. It has also been a source of significant controversy. The FDA has issued numerous statements against kratom, citing adverse events, potentially related deaths, risk of addiction or overdose, and incidences of contaminated supplements (3) (4) (5).

Kratom has both stimulant and sedative properties (6). The main psychoactive constituents are mitragynine and 7-hydroxymitragynine (7). In vivo studies of derivative compounds and analogs from kratom demonstrate antinociceptive effects (8). Animal models suggest that kratom has muscle relaxant (9), anti-inflammatory (10), analgesic (11), and anorectic (12) properties. Mitragynine has also shown antioxidant and antiproliferative effects in a few cancer cell lines (13).

Data on the use and safety of kratom in humans are very limited. Stimulant effects occur at lower doses, while sedative and pain-relieving effects occur at higher doses (14). Kratom users may develop physiological dependence and experience withdrawal (15), but this risk has not yet been adequately quantified (16). More research on the therapeutic uses for kratom and its constituents, as well as its toxic effects and abuse potential is needed.

The biological activities of kratom in humans are still poorly characterized (17). Because of its potential interactions with other drugs (18) (19) and possible side effects (20), kratom should not be used as a substitute for prescription pain medications. Several countries and US states have banned the use of kratom due to its potential for abuse (21) (22).

Purported Uses and Benefits
  • Anxiety
  • Insomnia
  • Pain relief
  • Stimulant
Mechanism of Action

The main active alkaloids in kratom are mitragynine and 7-hydroxymitragynine, which is thought to have analgesic effects comparable to morphine (11) (23). Through monoaminergic and opioid receptors, both compounds produce a range of CNS stimulant and depressant effects (23) (24) (25).

Although structurally different (26), mitragynine administration causes cognitive impairment and addiction profiles that closely resemble those of morphine (27). Other research also suggests these compounds share classic opioid characteristics — affinity for opioid receptors, analgesic cross-tolerance, and competitive interaction with naloxone — while possessing other novel attributes (28).

In animal models, anxiolytic-like effects are attributed to opioidergic, GABAergic, and dopaminergic interactions in brain regions (29). Mitragynine may also obstruct neuronal calcium channels (30).

Warnings
  • The FDA recently recalled powdered kratom supplements for salmonella contamination (5) and issued a public health advisory against kratom (3), with warnings of addiction and overdose risks similar to that of other opioids (4).
  • The Drug Enforcement Administration includes kratom on its Drugs of Concern list. These substances are not currently regulated by the Controlled Substances Act, but pose risks to persons who abuse them. In addition, the National Institute of Drug Abuse identified kratom as an emerging drug of abuse (31).
  • Herbal mixtures that contain synthetic compounds and kratom have been linked to altered behavior (32), hemorrhagic stroke (45) and multiple deaths (33).
Contraindications
  • Patients with tachycardia should avoid using kratom as laboratory studies suggest the potential for cardiotoxicity or exacerbation of Torsade de Pointes (34).
Adverse Reactions

Withdrawal symptoms: Flu-like symptoms such as nausea, vomiting, chills, sweats, muscle spasms and pain, decreased appetite, or diarrhea; anxiety, irritability, depressed mood, hot flashes, sleeping difficulty; symptoms are more likely with heavier use (15) (16) (35).

Case reports

Numerous adverse effects involving the use of kratom and mitragynine have been reported in the medical literature across the following categories (53):

  • Addiction, withdrawal symptoms (14) (36)
  • Depression/anxiety relapse
  • Cardiac or cardiorespiratory arrest (38) (49)
  • Cardiotoxicity (34)
  • Intracerebral hemorrhage
  • Kidney and/or liver injury (37) (50) (51)
  • Multiorgan dysfunction/failure
  • Psychosis
  • Rhabdomyolysis
  • Seizures
  • Transient paralysis
  • Overdose (34) and deaths (3) (34) (39) (40) (33) (41) (31) (46) (47) (48), some with multi-drug circumstances that confound conclusive interpretation (42)
Herb-Drug Interactions
  • CYP450 substrates: Increased clearance of drugs metabolized by CYP450 enzymes (18) (19). Kratom may also inhibit 2D6 (43) and induce 1A2 (44).
  • UGT substrates: Increased clearance of drugs metabolized by UGT1A6 with kratom use (18).
  • P-glycoprotein substrates: Mitragynine inhibits P-gp in vitro, and concurrent administration with psychoactive drugs that are P-gp substrates may cause significant toxicity (52).
References
  1. Hassan Z, Muzaimi M, Navaratnam V, et al. From Kratom to mitragynine and its derivatives: physiological and behavioural effects related to use, abuse, and addiction. Neurosci Biobehav Rev. Feb 2013;37(2):138-151.
  2. Sabetghadam A, Ramanathan S, Sasidharan S, et al. Subchronic exposure to mitragynine, the principal alkaloid of Mitragyna speciosa, in rats. J Ethnopharmacol. Apr 19 2013;146(3):815-823.
  3. U.S. Food and Drug Administration. 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. February 6, 2018.
  4. U.S. Food and Drug Administration. FDA oversees destruction and recall of kratom products; and reiterates its concerns on risks associated with this opioid. February 21, 2018.
  5. U.S. Food and Drug Administration. FDA orders mandatory recall for kratom products due to risk of salmonella. April 3, 2018.
  6. Fluyau D, Revadigar N. Biochemical Benefits, Diagnosis, and Clinical Risks Evaluation of Kratom. Front Psychiatry. 2017;8:62.
  7. Griffin OH, 3rd, Daniels JA, Gardner EA. Do You Get What You Paid For? An Examination of Products Advertised as Kratom. J Psychoactive Drugs. Nov-Dec 2016;48(5):330-335.
  8. Varadi A, Marrone GF, Palmer TC, et al. Mitragynine/Corynantheidine Pseudoindoxyls As Opioid Analgesics with Mu Agonism and Delta Antagonism, Which Do Not Recruit beta-Arrestin-2. J Med Chem. Sep 22 2016;59(18):8381-8397.
  9. Chittrakarn S, Keawpradub N, Sawangjaroen K, et al. The neuromuscular blockade produced by pure alkaloid, mitragynine and methanol extract of kratom leaves (Mitragyna speciosa Korth.). J Ethnopharmacol. Jun 16 2010;129(3):344-349.
  10. Shaik Mossadeq WM, Sulaiman MR, Tengku Mohamad TA, et al. Anti-inflammatory and antinociceptive effects of Mitragyna speciosa Korth methanolic extract. Med Princ Pract. 2009;18(5):378-384.
  11. Takayama H. Chemistry and pharmacology of analgesic indole alkaloids from the rubiaceous plant, Mitragyna speciosa. Chem Pharm Bull (Tokyo). Aug 2004;52(8):916-928.
  12. Kumarnsit E, Keawpradub N, Nuankaew W. Acute and long-term effects of alkaloid extract of Mitragyna speciosa on food and water intake and body weight in rats. Fitoterapia. Jul 2006;77(5):339-345.
  13. Goh TB, Koh RY, Mordi MN, et al. Antioxidant value and antiproliferative efficacy of mitragynine and a silane reduced analogue. Asian Pac J Cancer Prev. 2014;15(14):5659-5665.
  14. Diep J, Chin DT, Gupta S, et al. Kratom, an Emerging Drug of Abuse: A Case Report of Overdose and Management of Withdrawal. A A Case Rep. 2018 Apr 15;10(8):192-194.
  15. Singh D, Muller CP, Vicknasingam BK. Kratom (Mitragyna speciosa) dependence, withdrawal symptoms and craving in regular users. Drug Alcohol Depend. Jun 1 2014;139:132-137.
  16. Swogger MT, Walsh Z. Kratom use and mental health: A systematic review. Drug Alcohol Depend. Feb 1 2018;183:134-140.
  17. Kruegel AC, Grundmann O. The medicinal chemistry and neuropharmacology of kratom: A preliminary discussion of a promising medicinal plant and analysis of its potential for abuse. Neuropharmacology. 2018 May 15;134(Pt A):108-120.
  18. Azizi J, Ismail S, Mansor SM. Mitragyna speciosa Korth leaves extracts induced the CYP450 catalyzed aminopyrine-N-demethylase (APND) and UDP-glucuronosyl transferase (UGT) activities in male Sprague-Dawley rat livers. Drug Metabol Drug Interact. 2013;28(2):95-105.
  19. Maurer HH. Chemistry, pharmacology, and metabolism of emerging drugs of abuse. Ther Drug Monit. Oct 2010;32(5):544-549.
  20. Lydecker AG, Sharma A, McCurdy CR, et al. Suspected Adulteration of Commercial Kratom Products with 7-Hydroxymitragynine. J Med Toxicol. Dec 2016;12(4):341-349.
  21. Henningfield JE, Fant RV, Wang DW. The abuse potential of kratom according the 8 factors of the controlled substances act: implications for regulation and research. Psychopharmacology (Berl). Feb 2018;235(2):573-589.
  22. Adkins JE, Boyer EW, McCurdy CR. Mitragyna speciosa, a psychoactive tree from Southeast Asia with opioid activity. Curr Top Med Chem. 2011;11(9):1165-1175.
  23. Warner ML, Kaufman NC, Grundmann O. The pharmacology and toxicology of kratom: from traditional herb to drug of abuse. Int J Legal Med. Jan 2016;130(1):127-138.
  24. Rech MA, Donahey E, Cappiello Dziedzic JM, et al. New drugs of abuse. Pharmacotherapy. Feb 2015;35(2):189-197.
  25. Suhaimi FW, Yusoff NH, Hassan R, et al. Neurobiology of Kratom and its main alkaloid mitragynine. Brain Res Bull. Sep 2016;126(Pt 1):29-40.
  26. Prozialeck WC, Jivan JK, Andurkar SV. Pharmacology of kratom: an emerging botanical agent with stimulant, analgesic and opioid-like effects. J Am Osteopath Assoc. Dec 2012;112(12):792-799.
  27. Yusoff NH, Suhaimi FW, Vadivelu RK, et al. Abuse potential and adverse cognitive effects of mitragynine (kratom). Addict Biol. Jan 2016;21(1):98-110.
  28. Raffa RB, Beckett JR, Brahmbhatt VN, et al. Orally active opioid compounds from a non-poppy source. J Med Chem. Jun 27 2013;56(12):4840-4848.
  29. Hazim AI, Ramanathan S, Parthasarathy S, et al. Anxiolytic-like effects of mitragynine in the open-field and elevated plus-maze tests in rats. J Physiol Sci. May 2014;64(3):161-169.
  30. European Monitoring Centre for Drugs and Drug Addiction (EMCDDA). Kratom (Mitragyna speciosa) drug profile. Accessed April 1, 2022
  31. Anwar M, Law R, Schier J. Notes from the Field: Kratom (Mitragyna speciosa) Exposures Reported to Poison Centers - United States, 2010-2015. MMWR Morb Mortal Wkly Rep. Jul 29 2016;65(29):748-749.
  32. Arndt T, Claussen U, Gussregen B, et al. Kratom alkaloids and O-desmethyltramadol in urine of a “Krypton” herbal mixture consumer. Forensic Sci Int. May 20 2011;208(1-3):47-52.
  33. Kronstrand R, Roman M, Thelander G, et al. Unintentional fatal intoxications with mitragynine and O-desmethyltramadol from the herbal blend Krypton. J Anal Toxicol. May 2011;35(4):242-247.
  34. Lu J, Wei H, Wu J, et al. Evaluation of the cardiotoxicity of mitragynine and its analogues using human induced pluripotent stem cell-derived cardiomyocytes. PLoS One. 2014;9(12):e115648.
  35. Grundmann O. Patterns of Kratom use and health impact in the US-Results from an online survey. Drug Alcohol Depend. Jul 1 2017;176:63-70.
  36. Galbis-Reig D. A Case Report of Kratom Addiction and Withdrawal. WMJ. Feb 2016;115(1):49-52; quiz 53.
  37. Dorman C, Wong M, Khan A. Cholestatic hepatitis from prolonged kratom use: A case report. Hepatology. 2015 Mar;61(3):1086-7.
  38. Aggarwal G, Robertson E, McKinlay J, et al. Death from Kratom toxicity and the possible role of intralipid. J Intensive Care Soc. Feb 2018;19(1):61-63.
  39. Neerman MF, Frost RE, Deking J. A drug fatality involving Kratom. J Forensic Sci. Jan 2013;58 Suppl 1:S278-279.
  40. Holler JM, Vorce SP, McDonough-Bender PC, et al. A drug toxicity death involving propylhexedrine and mitragynine. J Anal Toxicol. Jan 2011;35(1):54-59.
  41. Karinen R, Fosen JT, Rogde S, et al. An accidental poisoning with mitragynine. Forensic Sci Int. Oct 24 2014;245c:e29-e32.
  42. Domingo O, Roider G, Stover A, et al. Mitragynine concentrations in two fatalities. Forensic Sci Int. Feb 2017;271:e1-e7.
  43. Hanapi NA, Ismail S, Mansor SM. Inhibitory effect of mitragynine on human cytochrome P450 enzyme activities. Pharmacognosy Res. Oct 2013;5(4):241-246.
  44. Lim EL, Seah TC, Koe XF, et al. In vitro evaluation of cytochrome P450 induction and the inhibition potential of mitragynine, a stimulant alkaloid. Toxicol In Vitro. Mar 2013;27(2):812-824.
  45. Nacca N, Schult RF, Li L, et al. Kratom Adulterated with Phenylethylamine and Associated Intracerebral Hemorrhage: Linking Toxicologists and Public Health Officials to Identify Dangerous Adulterants. J Med Toxicol. 2020 Jan;16(1):71-74.
  46. Hughes RL. Fatal combination of mitragynine and quetiapine - a case report with discussion of a potential herb-drug interaction. Forensic Sci Med Pathol. 2019 Mar;15(1):110-113.
  47. Gershman K, Timm K, Frank M, et al. Deaths in Colorado Attributed to Kratom. N Engl J Med. 2019 Jan 3;380(1):97-98.
  48. Matson M, Schenk N. Fatality of 33-Year-Old Man Involving Kratom Toxicity. J Forensic Sci. 2019 Nov;64(6):1933-1935.
  49. Abdullah HMA, Haq I, Lamfers R. Cardiac arrest in a young healthy male patient secondary to kratom ingestion: is this ’legal high’ substance more dangerous than initially thought ? BMJ Case Rep. 2019 Jul 19;12(7). pii: e229778.
  50. Aldyab M, Ells PF, Bui R, Chapman TD, Lee H. Kratom-Induced Cholestatic Liver Injury Mimicking Anti-Mitochondrial Antibody-Negative Primary Biliary Cholangitis: A Case Report and Review of Literature. Gastroenterology Res. 2019 Aug;12(4):211-215.
  51. Osborne CS, Overstreet AN, Rockey DC, Schreiner AD. Drug-Induced Liver Injury Caused by Kratom Use as an Alternative Pain Treatment Amid an Ongoing Opioid Epidemic. J Investig Med High Impact Case Rep. 2019 Jan-Dec;7:2324709619826167.
  52. Rusli N, Amanah A, Kaur G, et al. The inhibitory effects of mitragynine on P-glycoprotein in vitro. Naunyn Schmiedebergs Arch Pharmacol. 2019 Apr;392(4):481-496.
  53. PubMed search. Kratom case reports of adverse events. Accessed April 1, 2022.
Email your questions and comments to aboutherbs@mskcc.org.

Last Updated