Phenelzine (Nardil)

MAOI Antidepressantprescriptionoral · inferred

Irreversible, non-selective monoamine oxidase (MAO-A and MAO-B) inhibitor of the hydrazine class. Despite a short plasma half-life (~11 h), the covalent irreversible inactivation of MAO produces a pharmacodynamic effect lasting 2-3 weeks (time required for de novo enzyme synthesis). Particularly effective in atypical depression and treatment-resistant anxiety disorders including social phobia. Carries SERIOUS risks of serotonin syndrome (with serotonergic drugs) and hypertensive crisis (with dietary tyramine) that mandate a 2-week washout period between MAOI discontinuation and SSRI initiation, and lifelong avoidance of tyramine-rich foods and sympathomimetics.

Projected serum levels — 45 mg, once daily

Phenelzine (Nardil)
Phenelzine (Nardil) modeled serum levels, 45 mg once daily over 15 days Population-based pharmacokinetic estimate. Steady state reached after approximately 1 days. 0 12.5 25 37.5 50 Day 0 Day 4 Day 8 Day 11 Day 15 Time on a regular schedule ≈ steady state · day 1
Phenelzine (Nardil) modeled serum levels with a loading dose of 58.7 mg, then 45 mg once daily The first dose is larger so levels approach steady state faster. 0 12.5 25 37.5 50 Day 0 Day 4 Day 8 Day 11 Day 15 Time on a regular schedule

Maintenance schedule: 45 mg once daily (oral).

Loading schedule: 58.7 mg on day 1, then 45 mg once daily — reaching therapeutic levels sooner.

Modeled steady state after ~1 days: peak ≈ 46.3 mg, trough ≈ 12.4 mg body load. Population-based estimate over 15 days for a 45 mg dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.

Key facts

Category
MAOI Antidepressant
Route modeled
Oral
Model confidence
inferred
Half-life
11 h
Common dose
45 mg
Suggested maximum
90 mg/day
Reference dose range
15–90 mg (single dose)
Suggested cadence
once daily
Validated against
45 mg oral — Cmax 0.030 mg/L at 1.5 h

Documented interactions

  • danger
    1P-LSD (1-Propionyl-LSD) + Phenelzine (Nardil) Serotonin risk

    1P-LSD (1-Propionyl-LSD) and Phenelzine (Nardil) both have serotonergic activity. Risk of serotonin syndrome (hyperthermia, rigidity, autonomic instability, altered mental status).

  • danger
    25I-NBOMe + Phenelzine (Nardil) Serotonin risk

    25I-NBOMe and Phenelzine (Nardil) both have serotonergic activity. Risk of serotonin syndrome (hyperthermia, rigidity, autonomic instability, altered mental status).

  • danger
    2C-I (2,5-Dimethoxy-4-iodophenethylamine) + Phenelzine (Nardil) Serotonin risk

    2C-I (2,5-Dimethoxy-4-iodophenethylamine) and Phenelzine (Nardil) both have serotonergic activity. Risk of serotonin syndrome (hyperthermia, rigidity, autonomic instability, altered mental status).

  • danger
    2C-B (4-Bromo-2,5-dimethoxyphenethylamine) + Phenelzine (Nardil) Serotonin risk

    2C-B (4-Bromo-2,5-dimethoxyphenethylamine) and Phenelzine (Nardil) both have serotonergic activity. Risk of serotonin syndrome (hyperthermia, rigidity, autonomic instability, altered mental status).

  • danger
    3-MeO-PCP (3-Methoxyphencyclidine) + Phenelzine (Nardil) Serotonin risk

    3-MeO-PCP (3-Methoxyphencyclidine) and Phenelzine (Nardil) both have serotonergic activity. Risk of serotonin syndrome (hyperthermia, rigidity, autonomic instability, altered mental status).

  • danger
    4-AcO-DMT (Psilacetin) + Phenelzine (Nardil) Serotonin risk

    4-AcO-DMT (Psilacetin) and Phenelzine (Nardil) both have serotonergic activity. Risk of serotonin syndrome (hyperthermia, rigidity, autonomic instability, altered mental status).

Serum checks 120 modeled interaction pairings for phenelzine (nardil) across your whole stack — absorption conflicts, enzyme inhibition, and nutrient depletion included.

Research behind this entry

  1. The monoamine oxidase inhibitor, phenelzine, in the treatment of depressive-anxiety states: a controlled clinical trial Robinson DS et al. · Archives of General Psychiatry, 1973 DOI

    Landmark controlled trial demonstrating phenelzine's statistically significant superiority over placebo in treating depressive-anxiety states, establishing the clinical efficacy profile that would define MAOI use in…

  2. Phenelzine vs atenolol in social phobia: a placebo-controlled comparison Liebowitz MR et al. · Archives of General Psychiatry, 1992 DOI

    Pivotal RCT demonstrating phenelzine's marked superiority over both atenolol and placebo for social phobia (social anxiety disorder), with 64% response rate versus 23% placebo, establishing MAOIs as the gold-standard…

  3. Dietary restrictions and drug interactions with monoamine oxidase inhibitors: an update Flockhart DA · Journal of Clinical Psychiatry, 2012 DOI

    Authoritative clinical review of MAOI dietary and drug interactions, codifying the tyramine-restricted diet, serotonin syndrome risk with co-administered serotonergic agents, and the 2-week SSRI washout requirement that…

3 published studies referenced in the app, each with a plain-language summary.