Ibogaine for Health & Longevity - Quick Reference Sheet

Ibogaine for Health & Longevity

Created on 08/04/2026 – Quick Reference based on Evidence Review created using AI4L / Opus 5 Audit

A plant-derived compound whose single dose produces a day-long altered state and apparently lasting change. Clearest signals: rapid end of opioid withdrawal, craving reduction lasting months, better mood, trauma symptoms and thinking after repeated head impacts — nearly all from small studies without comparison groups. It has caused fatal heart-rhythm disturbances; screening and monitoring appear to reduce, not eliminate, that hazard. (Full Review)

Protocol

Standard single flood dose
10–20 mg/kg oral
Purified hydrochloride; most clinics 10–15 mg/kg.
Single versus split dosing
Single main dose
Preceded by a 100 mg test dose 1–3 hours earlier; optional 1–3 mg/kg booster on a subsequent day.
Timing within the day
Early morning, fasted
After an 8–12 hour overnight fast; peak and cardiac risk window fall within full staffing.
Time to effect
Mood, trauma and cognitive change
1 month
Larger at one month than immediately after treatment.
Opioid withdrawal
24–48 hours
Effects are essentially immediate.
Craving reduction
Within days
Craving commonly returns at two to three months.

Benefits

Contraindications
  • QT-prolonging medications without washout
  • Methadone or buprenorphine maintenance without prior conversion
  • Monoamine oxidase inhibitors
  • Alcohol or benzodiazepine withdrawal state
  • Current alcohol or benzodiazepine dependence
  • Congenital long QT syndrome; family history of sudden cardiac death before 50
  • Baseline QTc >450 ms (men), >460 ms (women)
  • Structural or coronary heart disease; heart failure New York Heart Association Class III–IV; myocardial infarction within 6 months
  • Uncorrected potassium <3.8 mmol/L or magnesium <0.75 mmol/L
  • Liver impairment, Child-Pugh Class B or C
  • Severe kidney impairment (eGFR <30 mL/min/1.73 m²)
  • Personal or first-degree family history of psychosis or bipolar I disorder
  • Active seizure disorder
  • Pregnancy or breastfeeding
Key Interactions
  • CYP2D6 inhibitors (paroxetine, fluoxetine, bupropion, duloxetine, quinidine, terbinafine; fluoxetine 5-week washout)
  • SSRIs (sertraline, paroxetine, citalopram) and SNRIs (venlafaxine, duloxetine, desvenlafaxine)
  • Benzodiazepines and alcohol
  • Over-the-counter medications (diphenhydramine, doxylamine, loperamide, dextromethorphan, cimetidine)
  • Supplements (St. John's wort, 5-HTP, L-tryptophan, S-adenosylmethionine, berberine, high-dose liquorice root, yohimbine, concentrated caffeine, grapefruit extract)
  • Magnesium and potassium repletion (monitor rather than avoid)
  • Other interventions (5-MeO-DMT, ketamine, kratom, fasting, ketogenic or diuretic protocols in the preceding week)

Risk & Side Effects

  • High: QT interval prolongation and ventricular arrhythmia; fatal outcome; acute ataxia, tremor and motor impairment; severe nausea and vomiting; prolonged and psychologically demanding altered state
  • Medium: Bradycardia and hypotension; loss of opioid tolerance and elevated overdose risk on relapse; post-treatment insomnia and fatigue
  • Low: Seizures; persistent psychiatric complications; cerebellar neurotoxicity; hepatic enzyme elevation
  • Speculative: Cumulative cardiac risk with repeated dosing; unknown effects on long-term neurodegenerative risk

Monitoring

Marker Target Why
Corrected QT interval (QTc), 12-lead electrocardiogram <430 ms (men), <440 ms (women) Window in which fatal arrhythmia occurs
Serum potassium 4.0–4.5 mmol/L Low potassium lengthens the QT interval
Serum and red blood cell magnesium Serum 0.85–1.05 mmol/L; red cell upper half of range Stabilises cardiac membranes
Ionised calcium 1.18–1.30 mmol/L Low ionised calcium prolongs QT
Alanine aminotransferase and aspartate aminotransferase <25 U/L (men), <20 U/L (women) Governs conversion to the active metabolite
Estimated glomerular filtration rate (eGFR) >90 mL/min/1.73 m² Governs metabolite elimination
CYP2D6 genotype and metaboliser status Normal (extensive) metaboliser Determines clearance, peak exposure and cardiac risk
Thyroid-stimulating hormone (TSH) 0.5–2.0 mIU/L Thyroid state alters conduction and QT
Complete blood count (haemoglobin, haematocrit) 13.5–15.5 g/dL (men), 12.5–14.5 g/dL (women) Anaemia reduces tolerance of bradycardia
Echocardiogram (structural assessment) Normal chambers; ejection fraction >55% Detects structural disease that makes arrhythmia lethal

Cadence: Baseline panel within 30 days; electrolytes and an electrocardiogram (ECG) repeated the morning of dosing. Continuous telemetry at least 48 hours; ECG with electrolytes at 24 and 72 hours and one week; liver and kidney function at four weeks; ECG plus full panel at three months, and at six to twelve months if abnormal or repeat treatment is contemplated.

Qualitative Assessment

  • Craving intensity and frequency: rated daily; the claim is durable reduction, not acute suppression
  • Sleep quality and continuity: disrupted for the first week, then baseline or better
  • Cognitive clarity: processing speed, word-finding and concentration
  • Emotional reactivity and mood stability: irritability, flatness or intrusive recollection
  • Motivation and anhedonia (a reduced ability to feel pleasure): effortful activity and pleasure in ordinary rewards
  • Behavioural flexibility in daily life: whether avoidance patterns and habits have changed