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Depressant

Kava

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Common dose · Oral70–150 mg TS

Dosage

Oral

SourceThresholdLightCommonStrongHeavy
TripSit–50–70 mg TS70–150 mg TS150–200 mg TS300 mg+ TS

NOTE: Doses are given for pure kavalactones, usually 5-20% of kava. TS

TripSit dose text

TripSit's factsheet also states its doses as text.

Oral Light: 50-70mg Common: 70-150mg Strong: 150-200mg Heavy: 300mg+ | NOTE: Doses are given for pure kavalactones, usually 5-20% of kava. TS

What dose are you on? (self-reported, unverified)
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Duration

TripSit factsheet

Onset
20-30 minutes TS
Duration
3-6 hours TS
Aftereffects
9-18 hours TS

Mixing

For best safety practice, don't mix this drug with other depressants.

Why: respiratory depression. PsychonautWiki says:

Quotes from PsychonautWiki, CC BY-SA 4.0.

Acute combinations: what happens when these are taken close together. Entries backed by a medical journal or agency are listed first.

Backed by medical journals

  • Hepatic Route drugs - Kava inhibits several liver enzymes in the CYP family. Consequentially, combining kava with drugs metabolized via CYP pathways, such as paracetamol, may cause adverse effects. For a list of medications click here A 2010 review concluded that it's possible that ethanol combined with kava may be the cause of kava hepatotoxicity.[15] PW⚠ PsychonautWiki lists this combination without a danger rating.
  • Anticoagulants - Kava may increase the risk of bleeding if taken with anticoagulants. Specifically the kavalactone kavain. A list of anticoagulants can be found here[16] PW⚠ PsychonautWiki lists this combination without a danger rating.
  • Antiplatelet - Kava may increase the risk of bleeding if taken with antiplatelet agents. Specifically the kavalactone kavain. A list of antiplatelet agents can be found here[16] PW⚠ PsychonautWiki lists this combination without a danger rating.

PsychonautWiki also lists dangerous combinations shared across a whole group (depressants) in a table this page does not copy. Read that list on PsychonautWiki.

Risks and toxicity

Studies have shown that kava can and will induce a low level of hepatic apoptosis similar to how paracetamol affects the liver and also can affect hepatic enzymes. Because of this, certain medications can make kava unsuitable and even dangerous for some users. Noble kava root alone can not, without consuming very large amounts of the substance, induce toxic levels and no overdose has ever been recorded. The consumption of 'noble' kava root has very low toxicity, however consumption 'tudei' kava and the stems and leaves of kava plants may increase the risk of liver damage. PW

Lethal dosage

Some research has been done into finding the LD₅₀ of kavalactones with results stating that around 300-400 Mg/Kg daily would be the likely lethal dose based on animal studies. [1] PW

Tolerance and addiction potential

Kava is known to produce a "reverse tolerance" in many users, in a similar fashion to substances like kanna. This means that continued use is required in order to experience full effects. Some users do not experience this. PW

Kava is traditionally regarded as non-addictive especially in comparison to other chemically related drugs such as benzodiazepines. In some Pacific Island communities, there is some record of people who have a psychological addiction to kava and drink it like an alcoholic drinks alcohol. PW

Testing

Awaiting sourceReagent reactions and test kit guidance from a harm reduction testing service.

Effects

Awaiting sourceSubjective and physical effects from PsychonautWiki or TripSit.

Overview

Kava or kawa (Piper methysticum: Latin "pepper" + Latinized Greek "intoxicating") is a crop of the western Pacific. The name kava refers to both the plant itself and the psychoactive beverage prepared from its rootstock. PW

Tropical evergreen shrub with large heart-shaped leaves and woody stems. Its thick roots are mashed or ground and made into a cold and bitter-tasting beverage used similarly to alcohol. It has a long history of ritual and recreational use in Pacific Polynesia and is now a common herbal product, used widely by those in certain societies as part of a 'Kava Culture.'[1] TS

Kava or kava kava (Piper methysticum: Latin 'pepper' and Latinized Greek 'intoxicating') is a plant in the pepper family, native to the Pacific Islands. The name kava is from Tongan and Marquesan, meaning 'bitter'. Kava can refer to either the plant or a psychoactive beverage made from its root. The beverage is a traditional ceremonial and recreational drink from Polynesia, Micronesia, and Melanesia. Nakamals and kava bars exist in many countries. Traditional kava is made by grinding fresh or dried kava root, mixing it with water or coconut milk, and straining it into a communal bowl. Outside the South Pacific, kava is typically prepared by soaking dried root powder in water and straining it. It is consumed socially for its psychoactive effects, comparable to those produced by alcohol but without significant cognitive impairment or addiction risk. Kava also produces a numbing sensation in the mouth.[2–7] WP

Kava consists of sterile cultivars clonally propagated from its wild ancestor, Piper wichmanii. It originated in northern Vanuatu, where it was domesticated by farmers around 3,000 years ago through selective cultivation. Historically, the beverage was made from fresh kava; preparation from dry kava emerged in response to the efforts of Christian missionaries in the 18th and 19th centuries to prohibit the drinking of kava.[8][9][10] WP

According to in vitro research, the pharmacological effects of kava stem primarily from six major kavalactones that modulate GABAA, dopamine, norepinephrine, and CB1 receptors, and inhibit MAO-B and ion channel mechanisms. Kava reduces short-term, situational anxiety, but its specific efficacy for generalized anxiety disorder appears to not be supported by the evidence.[2][6][8][11] WP

Many countries banned or restricted kava in 2002 due to safety concerns. The World Health Organization (WHO) subsequently reviewed kava's safety and concluded that moderate consumption of kava in its traditional form, as a water-based suspension of roots, presents an "acceptably low level of health risk". However, WHO and other health authorities have also concluded that consumption of kava extracts produced with organic solvents or excessive amounts of low-quality kava products may be linked to an increased risk of adverse health outcomes, including liver injury.[3][8][12][13][14] WP

A 2026 case report describes severe opioid-like withdrawal after heavy use of a product sold as “kava” whose label listed akuamma; testing of the same product found kratom derivatives and kavalactones. PubMed

History

Awaiting sourceHistory and culture from Wikipedia or PsychonautWiki, with their citations.

Pharmacology

Constituents

A total of 18 different kavalactones (or kavapyrones) have been identified to date, at least 15 of which are active. However, six of them, including kavain, dihydrokavain, methysticin, dihydromethysticin, yangonin, and desmethoxyyangonin, have been determined to be responsible for about 96% of the plant's pharmacological activity. Some minor constituents, including three chalcones—flavokavain A, flavokavain B, and flavokavain C—have also been identified, as well as a toxic alkaloid (not present in the consumable parts of the plant), pipermethystine. Alkaloids are present in the roots and leaves.[8][48][49][50] WP

Pharmacodynamics

The following pharmacological actions have been reported for kava and/or its major active constituents:[51] WP

  • Potentiation of GABAA receptor activity (by kavain, dihydrokavain, methysticin, dihydromethysticin, and yangonin).[51] WP
  • Inhibition of the reuptake of norepinephrine (by kavain and methysticin) and possibly also of dopamine (by kavain and desmethoxyyangonin).[51] WP
  • Binding to the CB₁ receptor (by yangonin).[52] WP
  • Inhibition of voltage-gated sodium channels and voltage-gated calcium channels (by kavain and methysticin).[51] WP
  • Monoamine oxidase B reversible inhibition (by all six of the major kavalactones).[51] WP

Methanolic leaf extracts of Hawaiian kava cultivars showed stronger binding inhibition to several CNS receptors—including GABAA, dopamine D2, opioid (μ, δ), and histamine (H1, H2)—than root extracts, suggesting that compounds beyond the main kavalactones may contribute to the pharmacological effects of kava leaves.[53] WP

Detection

Recent usage of kava has been documented in forensic investigations by quantitation of kavain in blood specimens. The principal urinary metabolite, conjugated 4'-OH-kavain, is generally detectable for up to 48 hours.[54] WP

Pharmacokinetics

Kavalactones are quickly absorbed in the gut and vary in bioavailability. They primarily act on brain areas like the limbic system, amygdala, and reticular formation, but their exact molecular mechanisms are not yet fully understood.[55] WP

Data on the pharmacokinetics of kavalactones remain limited. In animal studies, particularly in rats, kavain—the primary kavalactone found in traditional kava preparations—was shown to be well absorbed, with an estimated bioavailability of approximately 50%. In humans, kavain undergoes extensive hepatic metabolism, primarily via cytochrome P450 (CYP) enzyme-mediated pathways, followed by further phase II biotransformation processes such as sulfonation, glucuronidation, and glutathione (GSH) conjugation.[7] WP

In rats administered a 100 mg/kg bodyweight dose of kavain, over 90% was eliminated within 72 hours through urine and feces, either as unchanged compound or as metabolites. No evidence of bioaccumulation has been observed in rats, mice, or humans.[7] WP

Chemistry

Awaiting sourceFormula, structure and identifiers from PubChem.

User reports

Erowid erowid.org

Listings

Erowid Experience Vault listing

Link as published on TripSit's factsheet.

Top stories
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Bluelight bluelight.org

Listings
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Reddit reddit.com

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Pop culture

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Add a reference

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References

  1. Other clinical trials show that Kava significantly lowers anxiety compared to placebo - Mosby's Dental Drug Reference Ninth Edition 2010
  2. Journal / agency Kava. April 2025
  3. Journal / agency Kava. 10 April 2018
  4. Other Kava. 2025
  5. Journal / agency LaPorte, E.; Sarris, J.; Stough, C.; Scholey, A. Neurocognitive effects of kava (Piper methysticum): a systematic review. Human Psychopharmacology. 2011-03-01. doi:10.1002/hup.1180 · PMID 21437989
  6. Other Kava. 2025-05-05
  7. Other Food Standards Australia New Zealand. Supporting Document 1: Risk and Technical Assessment – Urgent Proposal P1057: Kava (Piper methysticum) Beverage for Traditional and Recreational Use. 10 December 2021
  8. Other Kava. 3 January 2018
  9. Other Lebot, Vincent; Merlin, Mark; Lindstrom, Lamont. Kava: The Pacific Elixir: The Definitive Guide to Its Ethnobotany, History, and Chemistry. 1997
  10. Journal / agency Vincent Lebot; Patricia Siméoni. Is the Quality of Kava (Piper methysticum Forst. f.) Responsible for Different Geographical Patterns?. Ethnobotany Research & Applications. 2004. doi:10.17348/era.2.0.19-28
  11. Other Kava for Generalized Anxiety Disorder. 2023
  12. Other Kava: a review of the safety of traditional and recreational beverage consumption. 2016
  13. Journal / agency Kuchta, Kenny; Schmidt, Mathias; Nahrstedt, Adolf. German Kava Ban Lifted by Court: The Alleged Hepatotoxicity of Kava (Piper methysticum) as a Case of Ill-Defined Herbal Drug Identity, Lacking Quality Control, and Misguided Regulatory Politics. Planta Medica. 2015-12-01. doi:10.1055/s-0035-1558295 · PMID 26695707
  14. Journal / agency Showman, A. F.; Baker, J. D.; Linares, C; Naeole, C. K.; Borris, R; Johnston, E; Konanui, J; Turner, H. Contemporary Pacific and Western perspectives on 'awa (Piper methysticum) toxicology. Fitoterapia. 2015. doi:10.1016/j.fitote.2014.11.012 · PMID 25464054
  15. Journal / agency Li, XZ; Ramzan, I. Role of ethanol in kava hepatotoxicity. Phytotherapy Research. April 2010. doi:10.1002/ptr.3046 · PMID 19943335
  16. Journal / agency E.I Magura, M.V Kopanitsa, J Gleitz, T Peters, O.A Krishtal, Kava extract ingredients, (+)-methysticin and (±)-kavain inhibit voltage-operated Na+-channels in rat CA1 hippocampal neurons, Neuroscience, Volume 81, Issue 2, 1997, Pages 345-351, ISSN 0306-4522
  17. Other Australia New Zealand Food Standards Code - Standard 2.6.3 - Kava. 5 October 2006
  18. Other Travelers from Fiji to Australia can now take more kava for social functions. 17 December 2019
  19. Other Import requirements: Kava. 1 December 2021
  20. Other Kava fact sheet. April 2005
  21. Other Kava. 12 December 2016
  22. Other Armbruster, Stefan. Islanders shocked as Australia moves to ban kava. 10 July 2015
  23. Other Kava legal in WA, marketed at troubled sleepers. 2017-02-13
  24. Other C.I.J.M. Ross-van Dorp. Besluit van 23 april 2003, houdende wijziging van het Warenwetbesluit Kruidenpreparaten (verbod op Kava kava in kruidenpreparaten). 2003
  25. Other Fiji takes kava ban fight to WTO. August 2005
  26. Other Bowman, Chakriya. The Pacific Island Nations: Towards Shared Representation
  27. Other Comeback unter strengen Auflagen. 16 August 2015
  28. Other Joshua, Jane. New Kava Challenge. 17 February 2016
  29. Other The Medicines for Human Use (Kava-kava) (Prohibition) Order 2002
  30. Other Garae, Len. Kava banned in Poland. Dec 27, 2017
  31. Other Rozporządzenie Ministra Zdrowia z dnia 17 sierpnia 2018 r. w sprawie wykazu substancji psychotropowych, środków odurzających oraz nowych substancji psychoaktywnych
  32. Other Kava zalegalizowana. Marihuana będzie następna?
  33. Other Koninkrijksrelaties, Ministerie van Binnenlandse Zaken en. Warenwetbesluit Kruidenpreparaten
  34. Journal / agency Final Assessment Report on Piper methysticum G. Forst., rhizoma. 21 November 2017
  35. Journal / agency Kava: A Human Health Risk Assessment. Technical Report Series No 30. 2016-05-25
  36. Other Dunne: Kava unaffected by Psychoactive Substances Bill
  37. Other Standard 2.6.3 – Kava – Food Standards (Proposal P1025 – Code Revision) Variation—Australia New Zealand Food Standards Code – Amendment No. 154 - 2015-gs1906 - New Zealand Gazette
  38. Journal / agency Marketed Health Products Directorate Heath Products and Foods Branch. Canadian Adverse Reaction Newsletter. 2002
  39. Other Listing of Drugs Currently Regulated as New Drugs (The New Drugs List). 26 May 2016
  40. Other Ingredients - Kava. 2017
  41. Other Kava. 14 June 2023
  42. Other Kava and its extracts banned in Singapore
  43. Other Poisons Rules - Singapore Statutes Online
  44. Journal / agency Consumer Advisory: Kava-Containing Dietary Supplements May be Associated with Severe Liver Injury. 25 March 2002
  45. Journal / agency Scientific Memorandum: Kava. 2020-08-11
  46. Other GRAS Determination for 'Awa
  47. Other Vanuatu - Legislation - Kava Act 2002
  48. Journal / agency Sarris J, LaPorte E, Schweitzer I. Kava: a comprehensive review of efficacy, safety, and psychopharmacology. Aust N Z J Psychiatry. 2011. doi:10.3109/00048674.2010.522554 · PMID 21073405
  49. Journal / agency Bunchorntavakul, C.; Reddy, K. R. Review article: herbal and dietary supplement hepatotoxicity. Alimentary Pharmacology & Therapeutics. 2013-01-01. doi:10.1111/apt.12109 · PMID 23121117
  50. Journal / agency Olsen LR, Grillo MP, Skonberg C. Constituents in kava extracts potentially involved in hepatotoxicity: a review. Chem. Res. Toxicol. 2011. doi:10.1021/tx100412m · PMID 21506562
  51. Journal / agency Singh YN, Singh NN. Therapeutic potential of kava in the treatment of anxiety disorders. CNS Drugs. 2002. doi:10.2165/00023210-200216110-00002 · PMID 12383029
  52. Journal / agency Ligresti A, Villano R, Allarà M, Ujváry I, Di Marzo V. Kavalactones and the endocannabinoid system: the plant-derived yangonin is a novel CB₁ receptor ligand. Pharmacol. Res. 2012. doi:10.1016/j.phrs.2012.04.003 · PMID 22525682
  53. Journal / agency Dinh LD, Simmen U, Bueter KB, Bueter B, Lundstrom K, Schaffner W. Interaction of various Piper methysticum cultivars with CNS receptors in vitro. Planta Med. 2001. doi:10.1055/s-2001-14334 · PMID 11458444
  54. Other R. Baselt, Disposition of Toxic Drugs and Chemicals in Man, 8th edition, Biomedical Publications, Foster City, CA, 2008, pp. 803–804
  55. Other Kava (Other Names: Ava, Intoxicating Pepper, Kawa Kawa, Kew, Sakau, Tonga, Yangona). April 2025

Text and values on this page are quoted from PsychonautWiki (CC BY-SA 4.0), Wikipedia (CC BY-SA 4.0), TripSit factsheets. Each value links to the exact revision it came from.