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Phenazepam

Phenazepam molecule structurePhenazepam molecule structure
7-Bromo-5-(2-chlorophenyl)-1,3-dihydro-1,4-benzodiazepine-2-one
Bonsai, Soviet Benzo, Fenaz, Panda, Bromdihydrochlorphenylbenzodiazepine
Chemical Class

Phenazepam is a benzodiazepine first developed in the Soviet Union in 1975.citation needed It is prescribed in Russia and other countries for psychiatric conditions including anxiety and schizophrenia, as well as for epilepsy, alcohol withdrawal, and surgical premedication. Phenazepam is notable for its exceptionally long duration of action and high potency. The substance has gained notoriety for problematic recreational use, with numerous reports of compulsive redosing and reckless behavior due to its subtle onset and extended effects.

Dosage & Duration

Dosage

Doses are population estimates that vary widely between individuals.

Threshold~0.5 mg
Light0.5-1 mg
Moderate1-2 mg
Strong2-3 mg
Heavy3+ mg
Bioavailability
80%1

Duration

Onset15-60 minutes
After Effects36 hours
Total18 hours

Subjective Effects

Legacy content. A statistically backed ontology from Mindstate Design Labs is coming soon.

The experience is dominated by heavy sedation, anxiolysis, and physical relaxation, with no reported alteration of sensory perception. Coordination becomes unreliable, and at higher doses recall of the period following ingestion can be substantially impaired.

Physical

Muscle relaxation, drowsiness, and hypnotic sedation are the primary physical effects, accompanied by dizziness and loss of coordination.

Hiccups

Coordination

Dizziness

Sedation

Cognitive

Anxiety is reduced and the mental state is markedly sedated, with anterograde amnesia becoming pronounced as dose increases.

Reagent Testing

Expected colorimetric results for common reagent tests. Colors show reaction change over 1–2 minutes.

Marquis(MQ)
white → orange1
Mecke(ME)
white → yellow2
Mandelin(MD)
No reaction
No reaction
Ehrlich(EH)
No reaction
No reaction
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Pharmacology

Pharmacodynamics

Phenazepam acts as a positive allosteric modulator at the benzodiazepine site of the GABA-A receptor.citation needed It is considerably more potent than diazepam, potentiating GABA responses with an EC50 of 6.1 nM in rat cerebellar slices versus 13.5 nM for diazepam. About 1 mg of phenazepam is reported to be equivalent to up to 10 mg of diazepam. The metabolite 3-hydroxyphenazepam is also pharmacologically active and potentiates GABA responses. The metabolites ABPH and QNZ exhibit biphasic activity at the GABA-A receptor, initially potentiating GABA at low concentrations and then inhibiting it at higher micromolar concentrations, so they are only likely to produce significant effects in overdose. ABPH is also thought to act at glycine and NMDA receptors at high micromolar concentrations.

Pharmacokinetics

Phenazepam is eliminated primarily by hepatic metabolism, with combined in silico and in vitro evidence identifying CYP3A4 as the most probable enzyme responsible and CYP3A5 as a possible contributor that could not be excluded.citation needed The main pathway is aromatic hydroxylation to 3-hydroxyphenazepam, alongside hydrolysis and glucuronide conjugation. After oral administration, phenazepam reaches a peak plasma concentration at about 4 hours and has an estimated bioavailability of roughly 80%. Its elimination half-life is reported between about 15 and 60 hours, spanning an oral estimate of roughly 60 hours and 14.9-15.6 hours following intramuscular or intravenous administration. The volume of distribution is 4.7-6.0 L and plasma clearance is 220.4-267.9 ml/h. In vitro, phenazepam also produced an observed but not statistically significant increase in CYP2B6 activity.

Interactions

Dangerous

Highest risk

These combinations are considered extremely harmful and should always be avoided. Reactions to these drugs taken in combination are highly unpredictable and have a potential to cause death.

AlcoholGHB/GBLOpioidsTramadol

Unsafe

Avoid

There is considerable risk of physical harm when taking these combinations, they should be avoided where possible.

Caution

Use caution

These combinations are not usually physically harmful, but may produce undesirable effects, such as physical discomfort or overstimulation. Extreme use may cause physical health issues. Synergistic effects may be unpredictable. Care should be taken when choosing to use this combination.

DXMKetamineMXE
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Tolerance

Tolerance timelines are rules of thumb, not exact schedules, and vary widely between individuals and use patterns.

Full Tolerance
Tolerance develops with regular use.citation needed Treatment courses are typically limited to two weeks due to the risk of dependence, suggesting clinically significant tolerance develops within this timeframe.
Cross Tolerance

Benzodiazepines2, GABAergic depressantscitation needed

Harm Potential

Addiction & Dependence

Psychological

High

High abuse potential with significant risk of psychological dependence.citation needed Anecdotal reports indicate a notable suggestibility for compulsive redosing and reckless usage patterns, particularly due to the drug's subtle onset and amnestic effects.

Physical

High

Physical dependence develops with regular use, and treatment courses are typically limited to two weeks due to dependence risk.citation needed Abrupt discontinuation following prolonged use can cause severe withdrawal symptoms including restlessness, anxiety, insomnia, seizures, convulsions, and potentially death. Due to its intermediate half-life and active metabolites, withdrawal symptoms may take two or more days to manifest.

Seizure Risk

Seizures and convulsions are documented withdrawal symptoms following abrupt discontinuation of prolonged use.3 Gradual dose reduction is necessary to prevent withdrawal-induced seizures.citation needed

History & Culture

Phenazepam is a benzodiazepine that was first developed in the Soviet Union in 1975.4 The synthesis method was developed at the Physico-Chemical Institute of the Academy of Sciences of the Ukrainian SSR during the 1970s. The substance is now produced in Russia and several

Legality

By Country

Illegal4
Canada flagCanadaIllegal (analog/blanket ban)
Netherlands flagNetherlandsIllegal
Sweden flagSwedenIllegal
United Kingdom flagUnited KingdomIllegal
Controlled / restricted4
Colombia flagColombiaRestricted
Denmark flagDenmarkRestricted
Latvia flagLatviaRestricted
Ukraine flagUkraineRestricted
Prescription5
France flagFrancePrescription only
Germany flagGermanyPrescription only
KazakhstanPrescription medication13
Lithuania flagLithuaniaPrescription only
Russia flagRussiaPrescription medication20
Legal / decriminalized1
Belarus flagBelarusLegal (regulated)

References

Source Pages

  1. Erowid: Phenazepam Law
  2. IsomerDesign: ACMD Advice on Phenazepam
  3. PsychonautWiki: Benzodiazepines
  4. TripSit Factsheet: Phenazepam
  5. Wikipedia

Citations

  1. Peter D. Maskell, Giorgia De Paoli, L. Nitin Seetohul, & Derrick J. Pounder. (April 2012). Phenazepam: the drug that came in from the cold. Journal of Forensic and Legal Medicine, 19(3), 122–5. https://doi.org/10.1016/j.jflm.2011.12.0141
  2. Addiction: Part I. Benzodiazepines — Side Effects, Abuse Risk and Alternatives. American Family Physician, April 2000.. (n.d.). https://www.aafp.org/pubs/afp/issues/2000/0401/p2121.html1
  3. Phenazepam 1 mg Tablets — Arpimed Prescribing Information. (n.d.). https://arpimed.am/phenazepam-1-mg-tablets/1
  4. Phenazepam Pre-Review Report, Agenda Item 5.8 — WHO Expert Committee on Drug Dependence, 37th Meeting. (2015). https://ecddrepository.org/sites/default/files/2023-04/5.8_phenazepam_prerev.pdf1
  5. Republican list of narcotic drugs, psychotropic substances and their precursors subject to state control in the Republic of Belarus (consolidated through Ministry of Health Resolution No. 18 of 10 March 2026). eec.eaeunion.org (n.d.). https://eec.eaeunion.org/upload/medialibrary/8fe/aqdeegj1xqca147n47vc4it72nlo2pok/BY_2026.pdf1
  6. Controlled Drugs and Substances Act, Schedule IV. laws-lois.justice.gc.ca (n.d.). https://laws-lois.justice.gc.ca/eng/acts/C-38.8/section-sched95660.html1
  7. Controlled Drugs and Substances Act. laws-lois.justice.gc.ca (n.d.). https://laws-lois.justice.gc.ca/eng/acts/C-38.8/FullText.html1
  8. Resolución 000116 de 2026. minsalud.gov.co (n.d.). https://www.minsalud.gov.co/Normatividad_Nuevo/Resolucion%20No%20116%20de%202026.pdf1
  9. Bekendtgørelse om euforiserende stoffer (BEK nr. 405 af 26. marts 2026). retsinformation.dk (n.d.). https://www.retsinformation.dk/eli/lta/2026/405/pdf1
  10. Arrêté du 4 novembre 2016 modifiant l’arrêté du 22 février 1990 fixant la liste des substances psychotropes. ansm.sante.fr (n.d.). https://ansm.sante.fr/uploads/2026/07/03/20260703-psychotropes-liste-consolidee.pdf1

Further Reading

  1. Drug-Do: Benzos - Phenazepam
  2. DrugWise: Phenazepam
  3. Drummer et al. (2012) - Phenazepam: The drug that came in from the cold
  4. Release: .org.uk - Phenazepam
  5. TALKTOFRANK - Phenazepam Effects

Article Status

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Recent changes8 human edits · latest

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21 August 2026

  1. Lyrea · Added a citation and reworded 11 words in PharmacologyPharmacodynamics

  2. Lyrea · Edited in PharmacologyPharmacokinetics

  3. Lyrea · Removed a citation and reworded 11 words in PharmacologyPharmacodynamics

  4. Lyrea · Reworded 16 words in PharmacologyPharmacodynamics

  5. Lyrea · Added a citation in Dosage & DurationRoutes 1 › Bioavailability

  6. Lyrea · Changed a word in Dosage & DurationRoutes 1 › Bioavailability

  7. Lyrea · Reworded 3 words in PharmacologyPharmacokinetics

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