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Lääkkeiden vuorovaikutukset

What laboratory studies, small human studies and case reports actually show about kava interactions.

Lyhyesti & Ytimekkäästi

Kava can interact with medicines and other central nervous system depressants. Laboratory findings show several possible CYP inhibitions, but small human studies do not confirm one uniform pattern across all enzymes. Alcohol and sedatives in particular should not be self-combined; regular medication warrants individual review.

Sytokromi-P450-järjestelmä

Sytokromi-P450-järjestelmä (CYP450) on entsyymiperhe maksassa, joka on vastuussa useimpien lääkkeiden metaboloitumisesta. Kun aine estää näitä entsyymejä, muiden aineiden hajoaminen hidastuu – niiden vaikutus ja sivuvaikutukset voivat näin ollen voimistua.

Miksi tämä on tärkeää?

Many medicines are metabolised by CYP enzymes. An in-vitro finding does not automatically mean clinically relevant inhibition in humans. Preparation, dose, duration and the medicine's therapeutic window determine practical relevance.

Mitä entsyymejä estetään?

Mathews et al. (2002) tested kava extract and individual kavalactones in human liver microsomes and found inhibition of several CYP enzymes. These are in-vitro findings, not clinical inhibition ratings in humans:

EntsyymiEstovoimaTärkeät substraatit (esimerkit)
CYP1A2In-vitro findingKofeiini, teofylliini, klozapiini, olantsapiini
CYP2C9In-vitro findingVarfariini, fenytoiini, tulehduskipulääkkeet (ibuprofeeni)
CYP2C19In-vitro findingomepratsoli, diatsepaami, klopidogreeli
CYP2D6In-vitro findingkodeiini, tramadoli, monet masennuslääkkeet
CYP3A4In-vitro findingBentsodiatsepiinit, statiinit, monet antibiootit

Kliininen merkitys

Russmann et al. (2005) reported reduced CYP1A2 activity in chronic users of traditional aqueous kava. Gurley et al. (2005; 12 healthy volunteers, 28 days, 138 mg kavalactones/day), by contrast, found reduced CYP2E1 but no significant change in CYP1A2, CYP2D6 or CYP3A4/5. The human findings are small and preparation- and consumption-dependent, so they cannot predict every medicine interaction.

Korkean riskin yhdistelmät

The following combinations should be avoided or medically reviewed in advance. Reasons differ: some involve additive CNS effects or case reports, while others have only mechanistic signals and no controlled combination trials.

⚠ Alkoholi

Risiko: AVOID

Concurrent use of kava and alcohol is not recommended:

  • 1.Additive CNS effects: Drowsiness, slower reactions and impaired coordination may increase.
  • 2.Liver risk not quantified: A combined liver risk has not been quantified reliably; the combination is avoided because of this uncertainty.
  • 3.Unpredictable intensity: Product, amount, drinking pattern and individual sensitivity make effects difficult to predict.

Do not use kava and alcohol together. The main practical reason is possible additive impairment of attention, reaction and coordination; the size of any additional liver risk is not reliably established.

⚠ Bentsodiatsepiinit & unilääkkeet

Risiko: PROFESSIONAL REVIEW

Do not combine benzodiazepines or Z-drugs with kava without medical review:

  • •Additive sedation: Drowsiness and psychomotor impairment may increase.
  • •CNS depression: Clinically relevant potentiation is possible; controlled combination trials are lacking.
  • •Interpret CYP findings: CYP3A4 inhibition was observed in vitro but not consistently confirmed in small human studies.

Tapausraportti: Almeida & Grimsley (1996) described a semicomatose state in a 54-year-old man after reported kava and alprazolam use. A single case report is a warning signal but does not establish mechanism or frequency.

⚠ Antipsykootit

Risiko: PROFESSIONAL REVIEW

Individual medical review is appropriate before kava use with antipsychotics:

  • •Sedation: Additive drowsiness or psychomotor impairment is possible.
  • •Case reports: Individual reports describe movement disorders; frequency and causality are unclear.
  • •CYP findings: Laboratory inhibition does not reliably predict the level of a specific medicine.

⚠ Veritulpat (verenvuotoa estävät lääkkeet)

Risiko: PROFESSIONAL REVIEW

Warfarin, phenprocoumon and other anticoagulants require professional review because of their narrow therapeutic window:

  • •Mechanistic signal: CYP2C9 inhibition was observed in vitro; a clinical kava-warfarin interaction has not been established in controlled studies.
  • •Monitor INR: Changes in co-used products should be coordinated with the treating clinician.
  • •Bleeding risk: The baseline risk of anticoagulation makes self-testing inappropriate.

Use kava with anticoagulation only after individual medical review.

Kohtalaisen riskin yhdistelmät

Seuraavat yhdistelmät vaativat varovaisuutta ja niitä tulisi käyttää vain lääkärin kanssa keskustelun jälkeen. Annoksen säätö voi olla tarpeen.

Masennuslääkkeet

Risiko: PROFESSIONAL REVIEW

SSRI:t (fluoksetiini, sertraliini, paroksetiini jne.):
  • • Pharmacokinetic interactions may occur depending on the product but are not clinically established as a class
  • • Serotonin syndrome from kava is not established as a typical clinical effect
  • • Additive drowsiness or dizziness are possible
SNRI:t (venlafaksiini, duloksetiini):
  • • Direct clinical combination data are limited
  • • Review co-medication individually rather than inferring from in-vitro CYP data
MAO-estäjät:
  • • MAO-B effects of individual kavalactones have been studied preclinically
  • • Pawa et al. (2026) found MAO-A inhibition by flavokawain A in an in-vitro enzyme assay; humans and combination with MAO inhibitors were not studied
  • • Do not self-combine with MAO inhibitors because medicine interactions can be serious
  • • Obtain medical review before use

Antikonvulsantit (epilepsialääkkeet)

Risiko: PROFESSIONAL REVIEW

Fenytoiini, karbamatsepiini, valproaatti ja muut antikonvulsantit:

  • •Pharmacokinetics: Altered levels are possible but cannot be predicted reliably for individual combinations.
  • •CNS effects: Additive drowsiness or coordination problems are possible.
  • •Seizure control: Changes in co-used products belong under professional supervision.

Epilepsian yhteydessä Kavaa tulisi käyttää vain lääkärin valvonnassa.

Parkinson-lääkkeet

Risiko: PROFESSIONAL REVIEW

Levodopa ja dopamiiniagonistit:

  • •Mechanism unclear: Blanket clinical dopamine antagonism by kava has not been established.
  • •Case reports: Individual reports describe worsening Parkinson symptoms; medical review is therefore needed.

With Parkinson's disease or related medication, use kava only after medical review.

Hepatotoksiset lääkkeet

Risiko: KOHTALAINEN

Lääkkeet, joilla on tunnettu hepatotoksinen potentiaali:

  • •Parasetamoli/asetaminofeeni: Erityisesti suurilla annoksilla ongelmallinen
  • •Statiinit: Atorvastatiini, simvastatiini jne. (CYP3A4-substraatit)
  • •Metotreksaatti: Immunosuppressiivinen lääke, jolla on maksatoksisuus
  • •Isoniatsidi: Tuberkuloosilääke

Additional liver risk is plausible but not quantified for every combination. Potentially hepatotoxic medication requires individual medical review.

Yhteenvetotaulukko vuorovaikutuksista

Aineiden luokkaEsimerkitRiskiMechanismi
AlkoholiEthanoliAVOIDPossible additive sedation and impaired coordination; liver risk not quantified
BentsodiatsepiinitDiazepami, loratsepaami, alpratsolaamiPROFESSIONAL REVIEWPossible additive CNS depression; one case report, no controlled combination trials
AntipsykootitHaloperidoli, olantsapiini, klozapiiniPROFESSIONAL REVIEWSedation or interactions possible; direct clinical data limited
VeritulpatVarfariini, fenprokuomoniPROFESSIONAL REVIEWNo controlled kava interaction established; narrow therapeutic window
SSRI:tFluoksetiini, sertraliini, paroksetiiniPROFESSIONAL REVIEWPossible sedation or pharmacokinetics; no established kava serotonin syndrome
AntikonvulsantitFenytoiini, karbamatsepiiniPROFESSIONAL REVIEWPossible additive CNS effects and unpredictable pharmacokinetics
Parkinson-lääkkeetLevodopa, dopamiiniagonistitPROFESSIONAL REVIEWCase reports of symptom worsening; no blanket dopamine antagonism established
StatiinitAtorvastatiini, simvastatiiniPROFESSIONAL REVIEWDirect clinical interaction data are lacking; review liver and medication context
OpioiditKodeiini, tramadoli, morfiiniAVOID / REVIEWPossible additive CNS depression
KofeiiniKahvi, energiajuomatCAUTIONHuman CYP1A2 findings are small and inconsistent

Käytännön suositukset

Tarkistuslista ennen Kavan käyttöä

  • 1.
    Tarkista lääkkeiden lista

    Tarkista kaikki nykyiset lääkkeet vuorovaikutusten varalta

  • 2.
    Konsultoi lääkäriä

    Säännöllisesti lääkkeitä käyttävien tulisi kysyä lääkäriltä ennen Kavan käyttöä

  • 3.
    Vältä alkoholia

    Do not use kava and alcohol together. The main practical reason is possible additive impairment of attention, reaction and coordination; the size of any additional liver risk is not reliably established.

  • 4.
    Aloita pienellä annoksella

    Do not experiment with a self-selected lower kava dose while taking medicines; obtain professional review of the combination.

  • 5.
    Seuraa oireita

    Kiinnitä huomiota epätavalliseen väsymykseen, huimaukseen tai muihin oireisiin

Jatka turvallisuusluvussa

Tutkimuksiin perustuva

Christopher McCurdy

University of Florida College of Pharmacy

Näytä profiili →

Tämä wiki on kuratoitu resurssi, joka syntetisoi tutkimusta vertaisarvioituista tutkimuksista ja asiantuntijatutkiloista. Sitä ei ole kirjoittaneet yllä luetellut tutkijat, vaan se perustuu heidän julkaistuihin töihin.

Tieteelliset Lähteet

Tämän sivun tiedot perustuvat seuraaviin tieteellisiin tutkimuksiin ja julkaisuisiin:

Cytochrome P450 2E1 (CYP2E1) Is the Principal Enzyme Responsible for Urethane Metabolism

Hoffler U., El-Masri H.A., Ghanayem B.I. (2003) – Journal of Pharmacology and Experimental Therapeutics

Katso tutkimusta

Kava: From Ethnology to Pharmacology

Yadhu N. Singh (Editor) (2004) – CRC Press

Katso tutkimusta
Last updated: 18. maaliskuuta 2026•New study added