What are the contraindications for the use of psilocybin?
The contraindications for the use of psilocybin, magic truffles, and magic mushrooms are the same and divided into physical and mental contraindications.
Physical contraindications These include pregnancy, kidney disease, diabetes, epilepsy, neurological disorders, high blood pressure, cardiovascular disease, cerebral hemorrhages, adrenal gland problems, and abnormal blood cells. These conditions can make the use of psilocybin dangerous or affect its effects.
Mental contraindications include schizophrenia, psychosis, borderline personality disorder, PTSD, and other severe mental illnesses. Individuals with these conditions should ideally not use psychedelics, as this can worsen symptoms or have a negative impact on mental health.
In addition, there are also contraindications for certain medication. Medications such as TCAs (for example, amitriptyline) and MAO inhibitors can interact with psilocybin and must therefore be tapered off in consultation with the prescribing physician before psilocybin is used. Others, such as Lithium, can be very dangerous in combination with psychedelics. Various medications for blood pressure and heart function can also cause dangerous interactions.
We screen our clients for known contraindications by means of the intake.
Read also: Psilocybin info page | Psilocybin therapy | psilocybin ceremony

The use of psilocybin — as applied in a psilocybin session or truffle ceremony — requires careful medical and psychological screening. Although many people benefit from psychedelic therapy, there are clear contraindications where use is advised against or even excluded. Below is an overview of the main risks, supported by both scientific sources and insights from Triptherapie.
1. Psychiatric history
Individuals with a personal or family history of psychotic disorders such as schizophrenia, schizoaffective disorder, or bipolar disorder type I are at increased risk of exacerbation or triggering of psychosis. Recent severe substance dependence (alcohol or drugs) can also negatively affect safety and outcome. Therefore, people with this background are usually excluded from participation in a truffle session or other psilocybin guidance (source).
2. Cardiovascular and neurological disorders
Psilocybin temporarily increases heart rate and blood pressure, which can be risky for people with untreated or severe cardiovascular disease such as arrhythmias, previous heart attacks, strokes, or severe hypertension. Epilepsy and other neurological disorders are also contraindications due to the risk of seizures (source).
3. Medication interactions
Various medications can have dangerous interactions with psilocybin. This applies particularly to:
4. Special population groups
Pregnant women and breastfeeding women are excluded due to a lack of safety data. Minors are also generally not eligible, because brain development continues well past puberty and the long-term effects of psilocybin on young brains are insufficiently known.
Summary
A psilocybin session is not suitable for people with:
At Triptherapie, all clients are therefore screened in advance via a mandatory intake form, so that safety, effectiveness, and suitability can be properly assessed. This ensures that your psychedelic journey — if you are suitable for it — becomes a safe and healing experience.
The contraindications for psilocybin are indeed of great importance and must be taken seriously. The existing lists are fundamentally correct, but more nuance is needed from both neuropharmacology and clinical practice.
Psychiatric contraindications are often misunderstood in the public debate. Schizophrenia and type I bipolar disorder are clear contraindications, but it is not as black and white as “ever had psychosis = never psilocybin”. There are subtle gradations.
Risk of psychosis: Psilocybin acts primarily via 5-HT2A receptors, leading to increased thalamic input and cortical desynchronization. This can exacerbate psychotic symptoms in people with a vulnerable predisposition. Nevertheless, individuals with mild depressive or anxious traits, without a personal or family history of psychosis, have a significantly lower risk than is often assumed. Moreover, studies, such as that by Hopkinset al., demonstrate that careful screening and preparation can further reduce the risk.
The distinction between a is also important acute psychosis and psychotic traits. People with borderline personality disorder (BPD) may experience brief pseudopsychotic symptoms under stress, but this is fundamentally different from a primary psychotic disorder. BPD is indeed a risk factor for psilocybin use, but primarily due to the potential destabilization of self-image. Ego dissolution in BPD can reinforce existing identity diffusion, which can be psychologically disruptive.
Psilocybin can increase blood pressure and heart rate, but the underlying mechanism is more nuanced than often thought. The drug does not act primarily sympathomimetic (like adrenaline), but causes:
Therefore, someone with well-controlled hypertension (for example, 140/90 mmHg on medication) must be assessed differently than someone with untreated high blood pressure. The general contraindication “hypertension” often fails to adequately address this nuance. With Triptherapie, this is carefully screened for; psilocybin is not automatically unsafe in these cases.
Epilepsy is not a uniform condition. Photosensitive epilepsy, in which flashes of light can trigger a seizure, has a different risk profile than temporal lobe epilepsy. Psilocybin can increase cortical excitability, which could theoretically trigger a seizure, but the actual risk varies significantly by subtype.
This is one of the most important but often underestimated areas.
Lithium: The combination with psilocybin is often considered dangerous. Lithium affects multiple neurotransmitter systems, and theoretically, this could lead to serotonin syndrome. However, to date, there are no documented cases in the clinical literature. The possibility exists, but the actual incidence is unknown.
SSRIs and SNRIs: This is where the large gray area lies. In various therapeutic studies (such as at UCSF), patients continue to use their SSRIs. Although an SSRI inhibits serotonin reuptake, in practice, psilocybin often appears to be less potent in this group, presumably due to receptor downregulation. The combination is generally not dangerous, but it is less effective.
MAO inhibitors: This combination is indeed downright risky. MAO inhibitors block the breakdown of serotonin, which means psilocybin can lead to a longer and stronger trip.
After stopping antidepressants, some receptors remain dysregulated. Research suggests that a waiting period of at least two weeks after tapering off SSRIs or SNRIs is advisable to allow the serotonergic receptors to resensitize. This can make the difference between a stable and a risky experience.
These are rightly absolute contraindications. Psilocybin crosses the placenta, and its effect on fetal neurogenesis is unknown. Use during pregnancy or breastfeeding is therefore advised against.
Psychological preparation is at least as important as the medical screening. Someone with unresolved trauma can enter an acute dissociation under psilocybin. This is not immediately medically dangerous, but it can cause significant psychological damage. Therefore, intake interviews, in which both medical and emotional stability are assessed, are essential.
Conclusion:
Standard contraindication lists are valuable as a first filter, but their practical application requires medical and psychological expertise. Not every contraindication automatically implies an absolute ban. Many risks do not arise from psilocybin itself, but from interactions with pre-existing conditions, medication, or insufficient preparation. A professional intake and guidance make the difference between risk and safety in this regard.