COMPOUNDS / ADAPTOGEN / KAVA KAVA
ADAPTOGEN

KAVA KAVA

MEDIUM RISK
BEST FOR:Anxiety●●●●●●●○○○7/10
KAVA KAVA · KAVA · PIPER METHYSTICUM · KAVA-KAVA · KAVALACTONES · KAVAIN · AWA · YAQONA · SAKAU · RAUSCHPFEFFER
AnxiolyticAdaptogenPacific IslandGABAergicHepatotoxicity RiskTraditional Medicine

Traditional Pacific Island root beverage with anxiolytic and sedative kavalactones; rare but serious hepatotoxicity risk.

ROUTE / DOSAGE
LOW120mg
STANDARD200-280mg
HIGH400mg+
Note: Dose refers to kavalactone content; traditional beverage dosing varies by cultivar strength
CYCLE
Max 4-8 weeks continuous use then break avoid daily heavy use
BIOAVAILABILITY
Variable oral kavalactones show moderate absorption with first-pass metabolism
ACTIVE DURATION
4-8h (subjective)
STORAGE
Room temperature dry away from light refrigerate prepared beverages
HALF-LIFE
~9 hours (plasma)
DURATION BREAKDOWN
Total4-8 hours
Onset20-45 min
Come up20-30 min
Peak1-2 hours
Offset2-3 hours
After effects2-4 hours
Duration varies by route, dose, and individual. Source: community reports.
§ 01 — EFFECTS
7 documented
Anxiolysis and stress reduction
Sedation and relaxation
Mild euphoria and sociability
Muscle relaxation
Analgesia
Improved sleep quality
Mild sensory enhancement
§ 02 — RISKS
Rare but severe hepatotoxicity including liver failure requiring transplant
Reversible dermopathy (dry scaly skin) with prolonged heavy use
Withdrawal syndrome with hyperactive delirium after heavy chronic use
Hyponatremia reported in heavy intoxication
CYP enzyme inhibition causing drug interactions
Potential for psychological dependence with escalating use
§ 03 — INTERACTIONS
Interaction data not yet available for this compound.
§ 04 — SCIENCE

Multiple placebo-controlled trials and a Cochrane meta-analysis suggest kava extract is superior to placebo for generalized anxiety disorder, with effect sizes of 0.59-0.99. Short-term use (4-8 weeks) at 120-280 mg/day kavalactones appears well tolerated with mild, transient adverse events. However, evidence is insufficient to confirm efficacy beyond placebo, and one negative trial exists. Rare but severe hepatotoxicity cases led to bans in several countries, though causative mechanisms remain unclear and may relate to non-root plant parts or poor extraction methods. A 2024 case report documented kava withdrawal syndrome requiring phenobarbital treatment in a heavy user, suggesting dependence potential with excessive consumption. Product standardization remains a major challenge.

§ 06 — SOURCES
[1]
Kava as a Clinical Nutrient: Promises and Challenges
pubmed.ncbi.nlm.nih.gov ↗
[2]
Kava Withdrawal Treated With Phenobarbital - A Case Report
pubmed.ncbi.nlm.nih.gov ↗
[3]
Kava for Generalized Anxiety Disorder: A Review of Current Evidence
pubmed.ncbi.nlm.nih.gov ↗
[4]
Kava: An Overview
pubmed.ncbi.nlm.nih.gov ↗
[5]
Kava-kava and Anxiety: Growing Knowledge About Efficacy and Safety
pubmed.ncbi.nlm.nih.gov ↗
[6]
Kava Extract for Treating Anxiety (Cochrane Review)
pubmed.ncbi.nlm.nih.gov ↗
[7]
Toxicity of Kava Kava
pubmed.ncbi.nlm.nih.gov ↗
[8]
Kava Consumption and Its Health Effects
pubmed.ncbi.nlm.nih.gov ↗
Disclaimer. Protokol.wiki is an informational reference. Nothing on this site is medical advice. Compounds listed may be unapproved, unregulated, or illegal in your jurisdiction. Consult a licensed physician before use. Data compiled from peer-reviewed literature.
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