LSD for Health & Longevity - Quick Reference Sheet

LSD for Health & Longevity

Created on 08/06/2026 – Quick Reference based on Evidence Review created using AI4L / Opus 5 Audit

A laboratory-made compound acting on serotonin receptors, producing a roughly eight-to-twelve-hour change in perception, emotion, and sense of self. Strongest evidence: lasting reduction in long-standing anxiety after one or two supervised full-strength sessions, and reduced heavy drinking after a single session. Very small scheduled amounts repeatedly fail to beat dummy treatment. Illegality and unverified supply remain practical limits. (Full Review)

Protocol

Dose
100 or 200 micrograms
Single oral dose in every modern trial. Splitting is not used and is actively counterproductive at full doses. The psycholytic model uses repeated doses of roughly 50 to 100 micrograms; low-dose schedules use 5 to 20 micrograms.
Best time of day
Morning, 8 to 10 a.m.
Standard across all trial protocols. An 8 to 11 hour duration started later runs into the night, and residual arousal interferes with sleep. Low-dose protocols follow the same logic.
Session structure
Supervised 8 to 12 hour dosing day
Two to three preparatory meetings, two attendants present on the day, and two to three integration meetings in the following weeks. A quiet room, eyeshades, and a curated music programme are treated as part of the intervention.
Time to effect
Long-standing anxiety
4 weeks
Measured at 4 and 16 weeks, not on the day. Present at the first post-session assessment and maintained rather than accumulating.
Alcohol misuse
First follow-up
After a single session added to an existing treatment programme. The effect attenuated by six months and was no longer significant at twelve.
Well-being and openness
Acute, sustained to 12 months
Mood elevation is acute. Increases in openness and self-rated well-being remain measurable at twelve months after one or two sessions in healthy volunteers.

Benefits

Contraindications
  • Personal history of schizophrenia, schizoaffective disorder, or bipolar I disorder, or a first-degree relative with any of these
  • Current psychotic or manic episode, or active suicidal ideation with intent
  • Uncontrolled hypertension (systolic above 140 mmHg or diastolic above 90 mmHg on repeated measurement), or a hypertensive emergency history
  • Unstable coronary artery disease, myocardial infarction within the last 6 to 12 months, decompensated heart failure (New York Heart Association Class III or IV), or a clinically significant arrhythmia
  • Moderate or greater valvular regurgitation, or prior exposure to another 5-HT2B agonist (fenfluramine, pergolide, long-term ergot-derived migraine medication)
  • Unrepaired aortic aneurysm or a history of aortic dissection
  • Seizure disorder
  • Severe hepatic impairment (Child-Pugh Class B or C)
  • Pregnancy and breastfeeding
  • Lithium or a monoamine oxidase inhibitor
  • Inability to arrange a supervised, protected 12-hour window with a sober attendant
Key Interactions
  • Selective serotonin reuptake inhibitors and serotonin-norepinephrine reuptake inhibitors (fluoxetine, sertraline, escitalopram, venlafaxine, duloxetine)
  • Tricyclic antidepressants (amitriptyline, imipramine, clomipramine)
  • Atypical and typical antipsychotics (risperidone, olanzapine, haloperidol)
  • CYP2D6 inhibitors (paroxetine, fluoxetine, bupropion, quinidine, terbinafine)
  • CYP3A4 inhibitors and inducers (ketoconazole, ritonavir, clarithromycin, grapefruit juice as inhibitors; carbamazepine, rifampicin, St John's wort as inducers)
  • Over-the-counter serotonergic agents (dextromethorphan, chlorpheniramine, high-dose diphenhydramine)
  • Stimulants, prescribed or otherwise (methylphenidate, amphetamine salts, caffeine at high intake, cocaine)
  • Supplements with additive serotonergic effect (St John's wort, 5-HTP, L-Tryptophan, S-adenosylmethionine, high-dose tryptophan-containing protein supplements)
  • Supplements that add cardiovascular load (yohimbine, synephrine, high-dose caffeine, ephedra-containing preparations)
  • Supplements and drugs that blunt the response (high-dose magnesium, exogenous melatonin, trazodone, some antihistamines)
  • Cannabis

Risk & Side Effects

  • High: Perceptual disturbance and loss of ordinary functioning for 8 to 12 hours; acute psychological distress during the session; acute cardiovascular and autonomic stimulation; rapid tolerance with repeated dosing
  • Medium: Precipitation or worsening of psychosis and mania; hallucinogen persisting perception disorder; blood pressure elevation and anxiety from repeated low-dose use; prolonged post-session destabilization
  • Low: Valvular heart disease from sustained 5-HT2B activation; accidental injury and behavioral harm while impaired; adulteration and misidentification of unregulated material
  • Speculative: Cumulative cardiac fibrosis below the threshold of clinical valve disease; unfavorable interaction with age-related serotonergic decline; effects on immune and inflammatory aging

Monitoring

Marker Target Why
Blood pressure 110–125 / 65–80 mmHg Determines tolerance of a several-hour pressor load
Resting heart rate 50–70 bpm Baseline for the 10–20 bpm acute rise; a high resting rate narrows the reserve
12-lead electrocardiogram (ECG) Normal sinus rhythm; corrected QT interval under 440 ms in men and 460 ms in women Detects arrhythmia and conduction abnormality that the acute autonomic load could unmask
Transthoracic echocardiogram No more than trace mitral or aortic regurgitation; no leaflet thickening The only test that could detect valve change from sustained 5-HT2B receptor activation
Alanine aminotransferase (ALT) 10–26 U/L Confirms hepatic capacity for a compound cleared entirely by the liver
Estimated glomerular filtration rate (eGFR) Above 90 mL/min/1.73 m² Establishes clearance capacity for metabolites and general physiological reserve
Thyroid-stimulating hormone (TSH) 0.5–2.0 mIU/L Thyroid dysfunction mimics both anxiety and depression and must be excluded before attributing symptoms or improvement to the intervention
High-sensitivity C-reactive protein (hs-CRP) Below 1.0 mg/L Baseline for the speculative anti-inflammatory hypothesis and a general cardiovascular risk marker
Prolactin 4–15 ng/mL in men; 4–23 ng/mL in non-pregnant women The compound acutely raises prolactin; a baseline distinguishes drug effect from a pre-existing pituitary abnormality
CYP2D6 genotype Normal (extensive) metabolizer status Poor metabolizer status predicts a longer, stronger exposure from a standard dose

Cadence: Full baseline panel 1 to 4 weeks before a first session. Full-dose model: blood pressure and heart rate at baseline, hourly during the session, and at the end; clinical review at 1 week and 4 weeks; metabolic and hepatic panel repeated at 3 months if more than one session is undertaken. Repeated low-dose regimen: blood pressure weekly at home, clinical panel at 3 months, echocardiogram at 12 months and then every 12 to 24 months for as long as dosing continues.

Qualitative Assessment

  • Anxiety and worry burden: frequency and intensity of anticipatory worry, and whether it interrupts activity
  • Mood stability and the presence of anhedonia (a loss of pleasure in things that were previously enjoyable): whether ordinary sources of enjoyment register
  • Sleep quality and total sleep time: disrupted on a full-dose night by design; a persistent change beyond the first week is a signal to reassess
  • Cognitive clarity and working capacity: whether next-day cognitive flexibility has returned; persistence beyond 48 hours is atypical
  • Alcohol and other substance intake: drinks per week and heavy-drinking days
  • Sense of psychological flexibility and openness: willingness to engage with previously avoided material
  • Persisting visual phenomena: trailing images, halos, or visual snow at any point after a session; any positive finding is a reason to stop
  • Quality and content of integration: whether the material from the session is being engaged with or avoided