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Hypertensive Emergency Secondary to Combining Psilocybin Mushrooms, Extended Release Dextroamphetamine-Amphetamine, and Tranylcypromine

Peter Kenneth Gillman, Brian S. Barnett, Curtis J. Koons, Vincent Van den Eynde, J. Alexander Bodkin

Journal of Psychoactive Drugs June 21, 2024 DOI: 10.1080/02791072.2024.2368617 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Case report Peer reviewed
Sample size 1
Population 42-year-old man with treatment-resistant major depressive disorder
Interventions Psilocybe cubensis mushrooms tranylcypromine extended-release dextroamphetamine-amphetamine
Dose 1 g
Topics Psilocybin
Keywords Tranylcypromine Dextroamphetamine Anesthesia Hallucinogen Pharmacology
Citations 9
Key findings Combining psilocybin mushrooms with a monoamine oxidase inhibitor and dextroamphetamine-amphetamine may cause hypertensive emergency and myocardial infarction, likely due to phenylethylamine in the mushrooms.

Abstract

Data on medication interactions with psychedelics are limited. Here we present what may be the first published report of a hypertensive emergency following the combination of psilocybin mushrooms with a monoamine oxidase inhibitor (MAOI). A 42-year-old man with treatment-resistant major depressive disorder took 1 g of Psilocybe cubensis mushrooms, while prescribed tranylcypromine, extended-release dextroamphetamine-amphetamine, and other medications. Approximately half an hour later, he developed severe hypertension with chest pain, palpitations, and headache. Upon hospital presentation, the electrocardiogram demonstrated ST-elevation. The patient was diagnosed with a myocardial infarction and treated with lorazepam, nitroglycerin, and aspirin. He subsequently underwent emergency cardiac catheterization, which revealed no significant cardiac abnormalities. Following overnight hospitalization, he was discharged home with no lasting physical sequelae. Though data are few, past studies suggest that classic serotonergic psychedelics (5HT-2A receptor agonists) such as dimethyltryptamine (DMT), lysergic acid (LSD), and synthetic psilocybin should not produce hypertensive emergency when combined with MAOIs. We suspect phenylethylamine, found in Psilocybe cubensis and other species of psilocybin mushrooms, interacted with tranylcypromine and dextroamphetamine-amphetamine to produce this hypertensive emergency. Patients prescribed MAOIs should be warned of the potential for hypertensive emergency when consuming psilocybin mushrooms, particularly when also prescribed norepinephrine releasers such as dextroamphetamine-amphetamine.

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