
Amanita muscaria, commonly known as the Fly Agaric, is one of the most iconic and visually distinctive mushrooms in the world — its vivid red cap dotted with white warts has permeated fairy tales, video games, holiday folklore, and ancient religious traditions alike. Despite its fame within psychedelic culture, Amanita muscaria is fundamentally different from psilocybin-containing "magic mushrooms" and represents an entirely distinct pharmacological class. Its primary active compounds, muscimol and ibotenic acid, act on the GABAergic and glutamatergic systems rather than serotonergic receptors, producing an unusual dissociative-deliriant experience unlike any classical psychedelic.
The experience produced by Amanita muscaria is notoriously unpredictable and difficult to characterize. Users commonly report a dream-like, sedated quality; distorted perception of size (macropsia and micropsia, sometimes called the "Alice in Wonderland effect"); vivid waking dreams; unusual body sensations; and, at higher doses, deep stuporous sleep punctuated by profound dreams. The experience lacks the visual geometry and cognitive acceleration typical of psilocybin or LSD. Many users find the effects disorienting and dysphoric rather than euphoric, and nausea is common, particularly from uncured mushrooms containing significant ibotenic acid.
Raw Amanita muscaria contains substantial ibotenic acid, which is a neurotoxin that contributes to the mushroom's unpleasant side effects including nausea, vomiting, and muscular twitching. When the mushroom is dried or heated, ibotenic acid undergoes decarboxylation to muscimol, a far more pharmacologically desirable and active compound. Proper preparation — typically slow drying at low temperatures — dramatically alters the potency and character of the experience. The community has developed considerable practical knowledge around preparation methods to maximize muscimol content and minimize ibotenic acid. This mushroom is legal in most jurisdictions worldwide but should be approached with caution, careful preparation, and significant dose conservatism.
Safety at a Glance
High Risk- Identification is Critical
- Prepare Properly — Cure Your Mushrooms
- Toxicity: Acute Toxicity Amanita muscaria is toxic but not typically lethal to healthy adults at recreational doses when proper...
- Overdose risk: LD50 of muscimol in rat is 45mg/kg orally and in mice is 20mg/kg orally. Since muscimol and ibote...
If someone is in crisis, call 911 or Poison Control: 1-800-222-1222
Dosage
oral
Duration
oral
Total: 5 hrs – 10 hrsHow It Feels
The onset of Amanita muscaria is slow and uncertain, unfolding over one to two hours with an ambiguity that makes the experience difficult to navigate from the start. The first sign is often a heaviness in the limbs, a gravitational pull that is not the comfortable weight of sedation but something stranger — a feeling of being anchored to the earth in a way that is both literal and symbolic. Nausea builds steadily, sometimes reaching a crescendo of violent purging. The stomach rebels against the mushroom's chemistry with a persistence that suggests the body knows, on some deep level, that this is not food but something else entirely.
As the active compounds take hold — muscimol acting on GABA receptors, ibotenic acid adding its excitatory complications — the experience enters territory that shares almost nothing with psilocybin mushrooms. The visual field begins to warp, but not with the geometric precision or colorful beauty of classical psychedelics. Instead, objects change size: a phenomenon called macropsia and micropsia creates a disorienting world where hands seem to grow enormous, rooms seem to shrink, and spatial relationships become unreliable. The famous Alice in Wonderland connection is not literary fancy — these perceptual distortions are the mushroom's genuine signature.
At peak, two to four hours in, the state becomes dreamlike in the most literal sense. The boundary between waking consciousness and sleep dissolves, and a kind of lucid delirium takes hold. People, objects, and scenes may appear that are not present. Conversations may be held with entities that exist only within the intoxication. Physical coordination deteriorates significantly — walking becomes a stumbling, uncertain affair. The body may feel alternately too large and too small, and a curious muscular twitching can develop, particularly in the face and hands.
The decline is protracted and often leads directly into heavy, exhausted sleep filled with extraordinarily vivid dreams. Waking may bring confusion, residual nausea, and a sense of having been somewhere genuinely strange — not the meaningful, insight-laden strangeness of serotonergic psychedelics but something more primal and less narratively coherent. The overall impression is of an ancient, unpredictable technology of consciousness — one that operates by rules older and less refined than the tryptamine and phenethylamine tools that modern psychonauts typically employ.
Subjective Effects
The effects listed below are based on the Subjective Effect Index (SEI), an open research literature based on anecdotal reports and personal analyses. They should be viewed with a healthy degree of skepticism. These effects will not necessarily occur in a predictable or reliable manner, although higher doses are more liable to induce the full spectrum of effects.
Physical Effects
Physical(14)
- Decreased libido— Decreased libido is a diminished interest in and desire for sexual activity, commonly caused by subs...
- Increased libido— A marked enhancement of sexual desire, arousal, and sensitivity to erotic stimuli that can range fro...
- Increased salivation— Increased salivation (hypersalivation or sialorrhea) is the excessive production of saliva beyond wh...
- Muscle relaxation— The experience of muscles throughout the body losing their rigidity and tension, becoming noticeably...
- Nausea— An uncomfortable sensation of queasiness and stomach discomfort that may or may not lead to vomiting...
- Pain relief— A suppression of negative physical sensations such as aches and pains, ranging from dulled awareness...
- Perception of bodily heaviness— Perception of bodily heaviness is the subjective feeling that one's body has become dramatically hea...
- Physical euphoria— An intensely pleasurable bodily sensation that can manifest as waves of warmth, tingling electricity...
- Pupil constriction— A visible narrowing of the pupil diameter (miosis) that reduces the size of the dark center of the e...
- Pupil dilation— A visible enlargement of the pupil diameter (mydriasis) that can range from subtle widening to drama...
- Respiratory depression— A dangerous slowing and shallowing of breathing that can progress from barely noticeable reductions ...
- Sedation— A state of deep physical and mental calming that manifests as a progressive desire to remain still, ...
- Seizure— Uncontrolled brain electrical activity causing convulsions and loss of consciousness -- a life-threa...
- Stimulation— A state of heightened physical and mental energy characterized by increased wakefulness, elevated mo...
Cognitive & Perceptual Effects
Visual(19)
- After images— A visual phenomenon in which a faint, ghostly imprint of a previously viewed image persists in the v...
- Colour enhancement— An intensification of the brightness, vividness, and saturation of colors in the external environmen...
- Colour shifting— The visual experience of colors on objects and surfaces cycling through continuous, fluid transforma...
- Depth perception distortions— Alterations in how the distance of objects within the visual field is perceived, causing layers of s...
- Double vision— The visual experience of seeing a single object as two separate, overlapping images, similar to cros...
- Drifting— The visual experience of perceiving stationary objects, textures, and surfaces as appearing to flow,...
- External hallucination— A visual hallucination that manifests within the external environment as though it were physically r...
- Geometry— The experience of perceiving complex, ever-shifting geometric patterns superimposed over the visual ...
- Internal hallucination— Vivid, detailed visual experiences perceived within an imagined mental landscape that can only be se...
- Magnification— A visual distortion in which objects appear larger or closer than they actually are, as though one's...
- Perspective distortions— Distortion of perceived depth, distance, and size of real objects, making things appear closer, furt...
- Perspective hallucination— A hallucinatory phenomenon in which the observer's visual perspective shifts from the normal first-p...
- Recursion— The visual field begins to repeat and nest within itself in a self-similar, fractal-like manner, as ...
- Settings, sceneries, and landscapes— The perceived environment in which hallucinatory experiences take place, ranging from recognizable l...
- Tracers— Moving objects leave visible trails of varying length and opacity behind them, similar to long-expos...
- Transformations— Objects and scenery undergo perceived visual metamorphosis, smoothly shapeshifting into other recogn...
- Visual acuity enhancement— Vision becomes sharper and more defined than normal, as though a slightly blurry lens has been broug...
- Visual acuity suppression— Vision becomes blurred, indistinct, and out of focus, as though looking through a smudged lens. Fine...
- Visual haze— A translucent fog or haze overlays the visual field, softening the environment and reducing clarity....
Cognitive(15)
- Amnesia— A complete or partial inability to form new memories or recall existing ones during and after substa...
- Analysis enhancement— A perceived improvement in one's ability to logically deconstruct concepts, recognize patterns, and ...
- Analysis suppression— Analysis suppression is a cognitive impairment in which the capacity for logical reasoning, critical...
- Anxiety— Intense feelings of apprehension, worry, and dread that can range from a subtle background unease to...
- Anxiety suppression— A partial to complete suppression of anxiety and general unease, producing a calm, relaxed mental st...
- Cognitive euphoria— A cognitive and emotional state of intense well-being, elation, happiness, and joy that manifests as...
- Conceptual thinking— A shift in the nature of thought from verbal, linear sentence structures to intuitive, non-linguisti...
- Confusion— An impairment of abstract thinking marked by a persistent inability to grasp or comprehend concepts ...
- Delirium— Delirium is a serious and potentially dangerous state of acute mental confusion involving disorienta...
- Depression— A persistent state of low mood, emotional numbness, hopelessness, and diminished interest or pleasur...
- Dream potentiation— Enhanced dream vividness, complexity, and recall, often occurring as REM rebound after discontinuing...
- Immersion enhancement— A heightened capacity to become fully absorbed and engrossed in external media such as music, films,...
- Introspection— An enhanced state of self-reflective awareness in which one feels drawn to examine their own thought...
- Memory suppression— A dose-dependent inhibition of one's ability to access and utilize short-term and long-term memory, ...
- Sleepiness— A progressive onset of drowsiness, heaviness, and the desire to sleep that pulls the individual towa...
Auditory(3)
- Auditory distortion— Auditory distortion is the experience of sounds becoming warped, pitch-shifted, flanged, or otherwis...
- Auditory hallucination— Auditory hallucination is the perception of sounds that have no external source — hearing music, voi...
- Auditory misinterpretation— Auditory misinterpretation is the brief, spontaneous misidentification of real sounds as entirely di...
Multi-sensory(2)
- Scenarios and plots— Scenarios and plots are the narrative structures that emerge within hallucinatory states — coherent ...
- Synaesthesia— Stimulation of one sense triggers involuntary experiences in another — seeing sounds as colors, tast...
Transpersonal(2)
- Existential self-realization— A sudden, visceral realization of the profound significance and improbability of one's own existence...
- Unity and interconnectedness— A profound sense that identity extends beyond the self to encompass other people, nature, or all of ...
Pharmacology
Primary Active Compounds
Amanita muscaria's psychoactive effects are driven by two principal alkaloids:
Muscimol (5-aminomethyl-3-isoxazolol) is the primary active compound and the one responsible for the sought-after effects. Muscimol is a potent, selective agonist at GABA-A receptors — the primary inhibitory ion channel receptors in the mammalian central nervous system. GABA-A agonism produces widespread CNS depression, sedation, anxiolysis, muscle relaxation, and altered sensory processing. Muscimol also acts as a partial agonist at GABA-B receptors and has some activity at serotonergic and opioidergic receptors. Its mechanism is fundamentally different from all classical psychedelics (5-HT2A agonists), dissociatives (NMDA antagonists), or deliriants (anticholinergics), placing Amanita muscaria in a pharmacological class of its own.
Ibotenic acid is a structural analog of glutamic acid that acts as an agonist at both NMDA and metabotropic glutamate receptors. In the CNS, glutamate agonism at NMDA receptors can cause excitotoxicity at sufficient doses. Ibotenic acid is responsible for many of the unpleasant effects of improperly prepared mushrooms — nausea, vomiting, excessive salivation, muscular twitching, and a dysphoric, agitated mental state. It is estimated to be approximately 5–10 times less potent than muscimol as a psychoactive compound. During drying or heating, ibotenic acid undergoes decarboxylation to muscimol at a rate depending on temperature and duration.
Pharmacokinetics
Muscimol is water-soluble and absorbed relatively rapidly after ingestion. Onset typically occurs within 30–90 minutes, with peak effects at 2–4 hours. Total duration is 4–8 hours, though deep sleep may extend the experience. A well-documented and unusual phenomenon is the psychoactive activity of urine from individuals who have consumed the mushroom — muscimol passes through the kidneys largely unmetabolized and reaches sufficient concentrations in urine to produce effects. This "urine recycling" practice is documented in Siberian shamanic traditions and has been reported in modern users.
Preparation and Potency Variability
Potency varies enormously between individual mushrooms, geographic populations, and seasons. Fly Agaric collected in different regions (European, North American, Siberian) may have substantially different alkaloid profiles. The community has converged on slow oven-drying at 170°F (77°C) or lower as the optimal preparation method, converting ibotenic acid to muscimol while preserving the compound's integrity. Some users report water extraction and evaporation to create more standardized preparations, though quantitative testing remains rare in practice.
Tolerance
Limited data exists on tolerance development for muscimol specifically. Cross-tolerance with other GABAergic compounds (benzodiazepines, alcohol, GHB) is theoretically plausible given the shared receptor target, though the mechanisms differ. No cross-tolerance with classical psychedelics exists due to the entirely different mechanism of action.
Detection Methods
Urine Detection
Amanita muscaria (fly agaric) contains ibotenic acid and muscimol as primary psychoactive compounds. These GABAergic/glutamatergic substances are NOT detected by standard immunoassay-based urine drug screens. Muscimol and ibotenic acid are not structurally related to any standard drug panel target. The urine detection window for muscimol is approximately 12 to 24 hours, as the compound is largely excreted unchanged. LC-MS/MS methods specific to muscimol and ibotenic acid exist in toxicology research contexts.
Blood and Serum Detection
Blood detection windows for muscimol are approximately 4 to 12 hours after ingestion. The short detection window reflects rapid renal clearance of unmetabolized muscimol. LC-MS/MS is required for blood quantification at the low concentrations involved.
Standard Drug Panel Inclusion
Amanita muscaria compounds are NOT included on any standard drug panel (5-panel, 10-panel, 12-panel, or extended panels). There is no cross-reactivity with any immunoassay target. Detection requires specific toxicological analysis that is only available at specialized reference laboratories, typically in the context of poisoning investigation.
Confirmatory Methods
LC-MS/MS with reference standards for muscimol and ibotenic acid is the confirmatory method. GC-MS may require derivatization. These analyses are not part of routine clinical or forensic workflows and are performed only when mushroom poisoning is clinically suspected.
Reagent Testing (Harm Reduction)
Standard reagent testing kits (Marquis, Mecke, Mandelin, Ehrlich) are not validated for Amanita muscaria compounds. The Ehrlich reagent shows no reaction (no indole ring). Identification of Amanita muscaria relies primarily on morphological mycological identification rather than chemical reagent testing.
Interactions
No documented interactions.
History
Ancient and Pre-Historical Use
Amanita muscaria holds a unique position in the history of human consciousness alteration — it may represent one of the oldest intentionally consumed psychoactive substances known. The mushroom's distinctive appearance and powerful effects have left marks across cultures separated by vast distances and time.
The most extensively documented traditional use comes from indigenous peoples of Siberia and the Russian Far East — the Koryak, Chukchi, Evenki, Yukaghir, and Kamchadal peoples among others. Shamans (known by various regional names) used the mushroom as a central sacrament in ceremonial and healing contexts, consuming dried specimens to enter trance states for divination, spiritual healing, and communication with spirits and ancestors. A particularly striking practice documented by multiple early European explorers and anthropologists — including Georg Wilhelm Steller (1774) and Stepan Krasheninnikov — was the consumption of the shaman's urine by participants, which remained psychoactive as muscimol passed through the body largely unmetabolized. This "urine recycling" practice represented a way for more people to access the experience when mushrooms were scarce.
The mushroom's role in Siberian shamanism was noted by travelers as early as the 17th century, with systematic documentation beginning in the 18th century. The ethnomycologist R. Gordon Wasson proposed in his 1968 work Soma: Divine Mushroom of Immortality that Amanita muscaria was the soma of the ancient Vedic texts — the sacred drink of the Rigveda praised as a god in its own right and consumed by Hindu priests in religious ritual. While Wasson's hypothesis remains controversial and debated by scholars, it sparked enormous academic and popular interest in the ethnomycology of the mushroom.
The Soma Hypothesis and Vedic Traditions
The Rigveda, composed approximately 1500–1200 BCE and one of the oldest religious texts in continuous use, contains 120 hymns dedicated to soma — a deity who is simultaneously a plant, a drink, and a cosmic principle. Soma is described as growing in the mountains, being pressed and filtered, and producing altered states of consciousness when consumed by priests. Multiple features of the soma description have been interpreted as consistent with Amanita muscaria: its mountain habitat, its distinctive appearance, the absence of roots (mushrooms were sometimes categorized separately from rooted plants in ancient taxonomies), and the urine-recycling practice potentially alluded to in certain hymns. Critics of the Wasson hypothesis have proposed alternative candidates including cannabis (Cannabis sativa), Syrian rue (Peganum harmala), and the Syrian rue/cannabis combination. No consensus has been reached, but the debate has produced valuable scholarship on ancient psychoactive traditions.
European Folklore and the Fly Agaric Name
In European folk tradition, Amanita muscaria accumulated a rich body of folklore and superstition. The common name "Fly Agaric" derives from its use as an insecticide — pieces of the mushroom placed in milk or water were used to stun or kill flies (Musca domestica), a practice documented in medieval herbals and still occasionally employed in parts of rural Europe. Some scholars have suggested the name relates to the belief that the mushroom caused madness ("fly" referring to mental disturbance in archaic German and Scandinavian usage), though the insecticide application is the more substantiated etymology.
The mushroom features prominently in Northern and Central European fairy tale traditions, often depicted as the classic "toadstool" at the feet of gnomes, fairies, and mystical creatures. The connection between Amanita muscaria and the figure of Father Christmas / Santa Claus has been argued by some researchers — notably John Rush and others — pointing to the shamanic costume traditions of Siberian peoples (red and white costume), the "flying" reindeer (reindeer reportedly consume the mushroom and shamans may have consumed the urine of intoxicated reindeer), and the tradition of delivering gifts from above. While this thesis has gained popular circulation, it remains speculative and contested by folklorists.
Wasson and the Modern Ethnomycological Era
R. Gordon Wasson's 1957 Life magazine article "Seeking the Magic Mushroom," documenting his experiences with psilocybin mushrooms in Oaxaca, launched public awareness of psychedelic mushrooms — but his earlier and later work on Amanita muscaria and the soma hypothesis established the academic field of ethnomycology. Wasson's work inspired a generation of researchers including Terence McKenna (who controversially proposed Amanita muscaria as the origin of human intelligence in his "Stoned Ape" hypothesis) and, later, the broader academic interest in entheogenic plants that continues today.
Contemporary Interest
The past decade has seen a substantial resurgence in Amanita muscaria interest, driven in part by the broad legality of the mushroom in most jurisdictions (it is not scheduled in the United States or most of Europe), online community development, and interest in GABAergic psychoactive compounds distinct from classical psychedelics. Commercial products including Amanita muscaria extracts, tinctures, and gummies have entered the legal supplement market, raising new questions about standardization, safety, and regulation.
Harm Reduction
Identification is Critical
Correct species identification is the most important safety consideration with Amanita muscaria. The deadly Amanita phalloides (Death Cap) and Amanita bisporigera (Destroying Angel) can grow in the same habitats and may superficially resemble various Amanita species to the untrained eye. Do not consume any mushroom you cannot confidently identify with multiple confirming characteristics. Consult multiple field guides and ideally obtain an expert identification before consumption. Amanita muscaria is most distinctive in its classic form — red cap with white warts — but color can fade with rain or age, and white-capped varieties (var. alba) exist.
Prepare Properly — Cure Your Mushrooms
The most important preparation step is proper drying. Raw Amanita muscaria contains substantial ibotenic acid, which causes nausea, vomiting, muscular twitching, and dysphoric delirium. Slow drying converts ibotenic acid to muscimol:
- Preferred method: Dry in an oven at 150–170°F (65–77°C) for several hours until fully desiccated. Too high a temperature (above 200°F) degrades both ibotenic acid and muscimol.
- Air drying at room temperature over several days also works but is slower and less reliable.
- Avoid: Eating fresh mushrooms. Boiling in water (the traditional "parboiling" detoxification method) leaches out water-soluble alkaloids including muscimol and thus reduces psychoactive potency without reliably reducing ibotenic acid.
Start Extremely Low
Potency varies dramatically between individual specimens, populations, and seasons. Community experience indicates that even experienced users sometimes misjudge dose:
- Threshold: 1–3 g dried
- Low: 3–6 g dried
- Moderate: 6–10 g dried
- Strong: 10–15 g dried (significant nausea risk; unpredictable in naive users)
For first experiences, 1–3 g dried, properly cured mushroom is a responsible starting point. Wait at least 2–3 hours before considering any redose, as onset is slow and variable.
Set, Setting, and Sitter
Unlike classical psychedelics, the Amanita muscaria experience is often characterized by sedation, confusion, and disorientation. Having a sober companion who is aware of what has been consumed is particularly important, as the state can involve prolonged unconsciousness-like deep sleep. Inform someone of your consumption and ensure you are in a safe physical location.
Avoid All Other CNS Depressants
Do not combine Amanita muscaria with alcohol, benzodiazepines, opioids, GHB, ketamine, or other sedatives. Additive CNS depression creates a genuine risk of respiratory depression.
Toxicity & Safety
Acute Toxicity
Amanita muscaria is toxic but not typically lethal to healthy adults at recreational doses when properly identified. The mushroom must be correctly distinguished from deadly Amanita species — most critically Amanita phalloides (Death Cap) and Amanita virosa (Destroying Angel) — which contain amatoxins that cause severe and often fatal liver and kidney failure. These species are among the deadliest mushrooms known and are responsible for the vast majority of fatal mushroom poisonings worldwide. Visual misidentification is a genuine and serious risk.
The estimated lethal dose for muscimol in humans is not well established, but no confirmed fatalities from Amanita muscaria consumption alone have been reliably documented in the medical literature. However, significant toxicity and medical emergencies have occurred, primarily from ibotenic acid at high doses and from misidentification.
Ibotenic Acid Toxicity
Raw or improperly dried Amanita muscaria can contain sufficient ibotenic acid to produce significant adverse effects:
- Nausea, vomiting, and abdominal cramping
- Excessive salivation and lacrimation
- Muscular incoordination and twitching
- Agitation, confusion, and delirium
- In severe cases: seizure-like activity (rare but documented)
Cholinergic Effects
Despite the common name "Fly Agaric," Amanita muscaria contains only trace amounts of muscarine — the compound responsible for the classic cholinergic toxidrome (SLUDGE syndrome: salivation, lacrimation, urination, defecation, GI distress, emesis). The anticholinesterase effects seen in Amanita muscaria poisoning are largely attributable to ibotenic acid's glutamatergic activity rather than true muscarinic agonism.
Drug Interactions
- GABAergic depressants (alcohol, benzodiazepines, GHB, opioids, ketamine): Combined CNS depression creates significant risk of respiratory depression and unconsciousness. Avoid all combinations.
- Stimulants: May mask sedation and lead to excessive dosing.
- SSRI/SNRI: Theoretical interactions through serotonergic modulation; insufficient data.
- MAOIs: Unpredictable; avoid.
Contraindications
- Impaired ability to confidently identify mushroom species
- Liver or kidney disease (reduced metabolism)
- History of epilepsy or seizure disorders
- Pregnancy
- Concurrent CNS depressant use
Overdose Information
LD50 of muscimol in rat is 45mg/kg orally and in mice is 20mg/kg orally.
Since muscimol and ibotenic acid are GABAA agonists, it may be harmful to combine it with other GABAergic depressants such as benzodiazepines or barbiturates. Ibotenic acid is also known to be a neurotoxin, acting via the NMDA receptor and metabotropic glutamate receptor. It is wise to dry amanitas in the oven or purchase pre-dried amanitas to ensure the ibotenic acid concentration is as low as possible.
One of the major dangers of Amanita muscaria is misidentifying it as a different species of mushroom. Several other mushrooms in the genus amanita are toxic. One such mushroom, the Amanita phalloides, better known as the death cap, contains α-amanitin and β-Amanitin, both of which are extremely potent RNA polymerase II and RNA polymerase III inhibitors which damage virtually every tissue in the body. As the name suggests, the Amanita muscaria contains the chemical muscarine, a muscarinic acetylcholine agonist which is known to cause seizures; however, the mushroom contains very low amounts that are highly unlikely to pose any significant harm.
Amanita muscaria mushrooms are not known to be addictive or dependence-forming, and reports even show that desire to redose goes down with usage, though there is no research on this topic.
It is strongly recommended that one use harm reduction practices when using this substance.
Amanita muscaria grows naturally and is legal to grow, sell and consume in most parts of the world. It is, however, restricted in some countries.
- Australia:** The muscimol present in Amanita muscaria is considered a Schedule 9 prohibited substance in Australia under the Poisons Standard (October 2015). A Schedule 9 substance is a substance which may be abused or misused and the manufacture, possession, sale or use of is prohibited by law except when required for medical or scientific research, or for analytical, teaching or training purposes with approval of C
Tolerance
| Full | Limited data — may develop with repeated use |
| Half | Unknown |
| Zero | Unknown |
Cross-tolerances
Legal Status
Amanita muscaria grows naturally and is legal to grow, sell and consume in most parts of the world. It is, however, restricted in some countries.
Australia:** The muscimol present in Amanita muscaria is considered a Schedule 9 prohibited substance in Australia under the Poisons Standard (October 2015). A Schedule 9 substance is a substance which may be abused or misused and the manufacture, possession, sale or use of is prohibited by law except when required for medical or scientific research, or for analytical, teaching or training purposes with approval of Commonwealth and/or State or Territory Health Authorities.
Sweden:** Muscimol is considered a Swedish schedule I substance by Narkotikastrafflagen (Narcotic Drugs Punishments Act) as of December 30, 2025.
United Kingdom:** It is illegal to produce, supply, or import this drug under the Psychoactive Substance Act, which came into effect on May 26th, 2016.
Responsible use
Naturally occurring sources
Amanita pantherina
Amanita muscaria* (Wikipedia)
Psychoactive Amanita mushroom (Wikipedia)
Legal status of psychoactive Amanita mushrooms (Wikipedia)
Psychoactive amanitas (Erowid)
Amanita muscaria (Drugs-Forum)
Amanitaceae.org
Tatiana Urkachen, A Siberian shaman explaining A. muscaria (Youtube)
Experience Reports (2)
Tips (5)
Keep a usage log for Amanita muscaria including dose, time, effects, and side effects. This helps you identify patterns and prevent problematic escalation.
Always start with a low dose of Amanita muscaria and work your way up. Individual sensitivity varies, and you cannot undo a dose once taken.
Do not confuse Amanita muscaria with Amanita phalloides (death cap) or Amanita virosa (destroying angel), which are lethally toxic. Proper mushroom identification is critical. If you are not absolutely certain of identification, do not consume. Amanita pantherina is another species sometimes confused with muscaria that contains the same active compounds but at much higher and more dangerous concentrations.
Amanita muscaria produces a fundamentally different experience than psilocybin mushrooms. It acts on GABA receptors, not serotonin, producing sedation, delirium, and dream-like altered states rather than classical psychedelic effects. Dosing is highly variable between specimens. Start extremely low with properly prepared material and have a sitter present. This is not a recreational substance.
Proper drying and preparation of Amanita muscaria is essential for safety. Drying converts neurotoxic ibotenic acid into the desired psychoactive compound muscimol. Dry at low temperatures (no higher than 170F/75C) with airflow until completely crisp. Some practitioners age dried specimens for 2-3 months before use to allow further conversion. Never consume raw or insufficiently dried caps.
Community Discussions (1)
See Also
Similar by Effects
References (2)
- Amanita muscaria - TripSit Factsheet
TripSit factsheet for Amanita muscaria
tripsit - Amanita muscaria - Wikipedia
Wikipedia article on Amanita muscaria
wikipedia