Manual for Ibogaine Therapy: Screening, Safety, Monitoring & Aftercare
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Foundational treatment manual establishing 15-20 mg/kg dosing, 48-hour monitoring, EKG screening, and inclusion/exclusion criteria that shaped all subsequent ibogaine protocols
Dosing: 15–20 mg/kg therapeutic; 2 mg/kg test dose; 25–300 mg/day low-dose (oral)
Safety data present: ELECTROLYTE
Contraindications: Significant cardiac artery blockage or history of myocardial infarction, Blood pressure >170/105 or <80/60; pulse >120 or <50 bpm, Uncontrolled hypertension, Concurrent drug use during treatment (potentiates opiate/stimulant toxicity), Active neurological or psychiatric disorders requiring treatment, Beck Depression Inventory score ≥24 (debated by contributing authors), Concomitant medications causing adverse interactions (anti-epileptics, antidepressants, neuroleptics), History of sensitivity or adverse reaction to ibogaine, Clinically significant abnormal laboratory values, GI, liver, or kidney disease compromising metabolism/excretion, Active peptic ulcer (nonfatal adverse events documented), Active tuberculosis, Pregnancy, Liver enzymes >400% above normal (NIDA threshold)