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PCP Facts

Dissociative; Arylcyclohexylamine; NMDA receptor antagonist

Description

PCP (phencyclidine) — Angel Dust, Wet, Sherman — is a synthetic dissociative of the arylcyclohexylamine class. It blocks glutamate signaling while amplifying dopamine activity, producing dissociation and a distinctly psychosis-like experience.[1]

Subjective effects include dissociation, analgesia, paranoid thoughts, hallucinations, amnesia, and loss of motor coordination. The experience is more agitated and reality-fracturing than Ketamine, with detachment coexisting alongside hostile arousal rather than tranquil withdrawal.

PCP produces dopamine-driven reinforcement and carries a narrow margin between recreational and dangerous doses.[2][3] It accumulates in fat tissue and redistributes unpredictably, with muscle breakdown occurring in roughly 70% of clinical poisoning cases.[3]

Dose and durationby route · individual sensitivity varies

Oral(mg)
Threshold< 2 mgLight3 – 7 mgCommon7 – 12 mgStrong12 – 20 mgHeavy20+ mg

Starts in 20 – 60 minLasts 4 – 8 hoursAfter-effects 12 – 48 hours

Body and dependence

Acute toxicity
High
Chronic toxicity
High
Physical dependence
Low
Psychological dependence
Moderate
Withdrawal
Mild
Compulsive redosing
Moderate

Tolerance

Builds
Moderate
Fully resets after
Not recorded
Carries over to
ketamine; dextromethorphan; MK-801; methoxetamine

Effectslikely at a common dose

Perception
Proprioceptive distortion; Sensory deprivation; Spatial disorientation; Vestibular distortion; +12 possible, including Double vision, Visual acuity suppression, Visual haze / noise
Body
Body schema distortion; Motor control impairment; Nystagmus (eye wobbles); Pain suppression; +28 possible, including Dizziness, Temperature dysregulation, Vasoconstriction
Thinking
Cognitive impairment; Confusion; Decision impairment; Information processing suppression; Memory fragmentation; Memory suppression; Thought disorganization; +15 possible, including Analysis suppression, Language suppression, Compulsive redosing urge
Feeling
none likely · 11 possible, including Paranoia, Anxiety, Dysphoria
Self
Depersonalization; Derealization; +7 possible, including Communication suppression, Social disconnection, Craving
Time
Temporal disorientation; +2 possible

Who shouldn't take it

Absolute
Hypertension; Epilepsy; Psychotic disorders; Renal impairment; Pregnancy
Relative
Bipolar disorder; Hepatic impairment

Combinations68 recorded

Lethal (9)
5-MeO-DALT; 5-MeO-DiPT; 5-MeO-DMT; 5-MeO-MiPT; Dextromethorphan; GHB, GBL; Ibogaine; Tramadol; αMT
Dangerous (41)
Benzodiazepines; Buprenorphine, Kratom; Ephedrine, Pseudoephedrine; MDMA, Amphetamines; Naltrexone; NDRIs (Wellbutrin); NRIs; NSAIDs; Opioids; THC; 5-HTP, Tryptophan; Alpha-2 adrenergic receptor antagonist; Amphetamines; Anticholinergics; Antihistamines; Atypical antipsychotics; Benzodiazepines, Barbiturates; Buspirone; Caffeine; Cannabis; Cannabis, THC; CBD; Dopamine agonists; DXM; and 17 more, see full page
Caution (15)
See full page: psychedex.org/substances/pcp
Not graded (3)
Not listed never means safe.

Seek help immediately if

  • Severe disorientation; unable to move or speak (deep dissociation / "k-hole")
  • Complete loss of coordination — cannot stand or walk safely
  • Vomiting while incapacitated (choking / aspiration risk)
  • Very high blood pressure; fast heart rate
  • Slow or shallow breathing at high doses (especially mixed with depressants)
  • Unconsciousness; rarely, seizures

What to do

  1. Move them somewhere safe, away from stairs, water, roads, and sharp edges — they cannot protect themselves
  2. Place in the recovery position if vomiting or unconscious (aspiration is a key risk)
  3. Stay with them and reassure calmly; keep the environment quiet
  4. If breathing is slow/shallow or they are unresponsive, call emergency services
  5. Do not let them wander; do not leave them alone
  6. Be ready to give rescue breaths / CPR

Effects wear off with time in a safe, monitored setting. The main dangers are physical injury and aspiration while incapacitated, and respiratory depression when combined with other depressants — not the dissociation itself.

988 Suicide & Crisis LifelineFireside Project: 62-FIRESIDE

Version r1 · Not medical advice

References

  1. [1]
    ^Seeman P, Ko F, Tallerico T (2005) Dopamine receptor contribution to the action of PCP, LSD and ketamine psychotomimetics — Molecular Psychiatry PMID:15852061
  2. [2]
    ^Nicholson KL, Mansbach RS, Menniti FS, Balster RL (2007) The phencyclidine-like discriminative stimulus effects and reinforcing properties of the NR2B-selective NMDA antagonist CP-101 606 in rats and rhesus monkeys. — Behavioural Pharmacology PMID:17989511
  3. [3]
    ^abStatPearls (2023) Phencyclidine Toxicity Link
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