Kratom

Mitragynine / 7-Hydroxymitragynine (from Mitragyna speciosa)

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Kratom is a tropical tree native to Southeast Asia (Malaysia, Thailand, Indonesia) containing alkaloids with opioid-like and stimulant properties. At low doses (1-5g), produces stimulant effects: energy, alertness, increased sociability. At moderate doses (5-15g), produces opioid-like effects: euphoria, analgesia, sedation. At high doses (15g+), produces strong sedation and intense euphoria. Biphasic dose-response: stimulant at low end, opioid-like at high end. Legal status varies by jurisdiction; banned in some US states and countries, legal/unregulated in most others. Withdrawal similar to mild opioid withdrawal.

How It Works

Kratom contains 40+ alkaloids, primarily mitragynine (0.3-0.7%) and 7-hydroxymitragynine (0.01-0.04%). Mitragynine acts as a partial agonist at mu, delta, and kappa opioid receptors and also acts as an agonist at 5-HT7 and 5-HT2A serotonin receptors, and adrenergic receptors. 7-Hydroxymitragynine is a more potent opioid agonist. At low doses, adrenergic effects dominate (stimulation). At high doses, opioid effects dominate (sedation, analgesia). Complex polypharmacology makes effects dose-dependent and variable.

Legal Status

Legal in most US states (as of 2026), but banned in some: Tennessee, Alabama (previously), and several others; regulation ongoing. Some countries ban it (Thailand, Malaysia). Typically sold as botanical supplement; not FDA-regulated. Legal status subject to change.

Dosage Guide (Oral (powder))

LevelAmount (g)
Threshold1-2
Light2-5
Common5-10
Strong10-15
Heavy15-30

Note: Biphasic: 1-5g = stimulant effects. 5-10g = balanced effects. 10-15g = opioid-like effects. 15g+ = strong sedation. Individual sensitivity varies significantly; body weight, tolerance, and alkaloid strain variability affect dosing. Kratom potency varies 2-3x depending on strain and vein color. Red vein = more sedating. White vein = more stimulating. Green vein = balanced. Capsule dosing requires calculation: each capsule ~0.5g. Extracts are 10-50x more concentrated. Tolerance develops rapidly with daily use (weeks). Dose escalation common in chronic users.

Organ System Impacts

cardiovascular — Low
Low-dose use causes mild stimulation: increased heart rate, slight blood pressure elevation. High-dose use causes bradycardia (slower heart rate) and hypotension. Arrhythmias reported rarely. Most users experience minimal cardiovascular impact.
neurological — Moderate
Opioid-like effects on CNS. Low dose stimulates; high dose depresses. Chronic use associated with tolerance, psychological dependence, and potential cognitive changes. Withdrawal produces dysphoria, anxiety, irritability. No major neurotoxicity documented but long-term effects unknown.
ocular — Low
Miosis (pupil constriction) typical. Rarely, visual disturbances reported. No evidence of retinal toxicity or long-term ocular damage.
dermatological — Low
Itching (pruritus) common, especially at higher doses — opioid-like effect. Skin flushing possible. No documented dermatological toxicity.
respiratory — Low
High-dose use may cause mild respiratory depression but much less than pharmaceutical opioids. Rare case reports of severe respiratory depression at extremely high doses. Generally safe for respiratory function.
hepatic — Low
Rare case reports of hepatotoxicity (liver damage), mostly with chronic high-dose use. Some products may contain contaminants or additives (heavy metals reported in some samples). Most users experience no liver damage. Liver function testing recommended for chronic heavy users.
hematological — Low
No direct hematological effects documented. Rare case reports of thrombocytopenia (low platelets) but causality unclear. Generally no impact on blood cell counts.
renal — Low
Rare case reports of acute kidney injury with chronic heavy use, particularly in context of dehydration. Generally kidney-safe. Chronic high-dose users should maintain hydration.
gastrointestinal — Moderate
Nausea very common, especially early use and with powder (tolerance to nausea develops). Constipation from opioid-like effects on GI motility. Stomach upset, cramping, dry mouth common. Opioid-like GI slowing at higher doses.
musculoskeletal — Low
Muscle relaxation at higher doses. No documentation of musculoskeletal damage or rhabdomyolysis. Withdrawal may cause muscle aches.

Effects

Desired Effects

Negative Effects

Rare but Serious

Drug Interactions

Alcohol (Ethanol) — moderate

Additive CNS depression at high kratom doses. Impaired judgment, increased sedation, respiratory depression risk. Nausea exacerbated. Avoid combination, especially at higher kratom doses.

Opioids (Heroin, Fentanyl, Hydrocodone, Codeine) — moderate

Additive opioid effects and respiratory depression risk. Both have opioid activity. Increased overdose risk, especially with potent opioids like fentanyl. Combination increases addiction risk and potential for severe respiratory depression.

Benzodiazepines (Alprazolam, Diazepam, Lorazepam) — moderate

CNS and respiratory depression. Both depress CNS. Increased risk of oversedation, respiratory depression, loss of consciousness. Avoid combination.

Other CNS Depressants (GHB, Barbiturates, Z-drugs) — moderate

Additive depression of CNS. Respiratory depression, excessive sedation, overdose risk. Kratom at high doses already depresses CNS; combination increases danger.

CYP3A4/2D6 Substrate Drugs — moderate

Kratom may inhibit CYP3A4 and CYP2D6 enzymes. May increase blood levels of drugs metabolized by these pathways (many antidepressants, pain meds, antiarrhythmics). Consult pharmacist about specific drug interactions.

Anticholinergic Drugs (Antihistamines, Antispasmodics) — moderate

Additive anticholinergic effects. Increased constipation, urinary retention, dry mouth, potential confusion at high doses.

Stimulants (Cocaine, Methamphetamine, Amphetamine) — low

Opposing effects but manageable. Kratom's opioid effects at high doses may combine with stimulant's cardiovascular effects. Not as dangerous as opioid-stimulant combos but avoid at extreme doses of either.

SSRIs (Fluoxetine, Sertraline, Paroxetine) — low

Minimal interaction. Kratom has some serotonergic activity but unlikely to cause serotonin syndrome with typical SSRI doses. Monitor for increased serotonergic effects.

Detection Times

Kratom (mitragynine) is not detected on standard drug panels. Specialized testing exists.

Urine

Requires specific kratom/mitragynine test. Not on standard panels. Detection window: up to 7 days.

Blood

Blood testing for mitragynine. Detection window: up to 3 days.

Hair

Hair testing for kratom alkaloids. Detection window: up to 90 days.

Harm Reduction Tips

Withdrawal Symptoms

Severity: Moderate

Onset: 12-24 hours. Peak: days 2-4. Acute phase: 5-7 days. Protracted symptoms (mood, cravings): 2-4 weeks.

Physical

Psychological

Emergency Information

Call 911 If:

Warning Signs

What To Do

  1. Move person to safe location.
  2. Check airway, breathing, circulation. Perform CPR if needed.
  3. Place in recovery position if unconscious.
  4. Monitor vital signs: breathing rate, heart rate, blood pressure.
  5. Keep person hydrated if conscious (small sips).
  6. Cool person if overheated (though hyperthermia rare with kratom).
  7. Keep person calm and reassured.
  8. Have medical history and kratom dose information ready for paramedics.
  9. Do not leave person alone.
Harm reduction information only. This is not medical advice. If you are experiencing a medical emergency, call 911 immediately.