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Clonazolam Facts

Depressant; Anxiolytic; Sedative; Benzodiazepine; GABA-A receptor positive allosteric modulator

Description

Clonazolam is a synthetic depressant of the triazolobenzodiazepine class. It amplifies GABA, the brain's primary inhibitory signal, broadly suppressing nervous system activity and producing sedation, anxiety relief, and muscle relaxation.[1]

Subjective effects include sedation, muscle relaxation, anxiety suppression, disinhibition, and dense amnesia. The defining quality is a gap between how impaired a person feels and how impaired they actually are — a pervasive calm that masks severe cognitive and motor deficits.

Clonazolam produces rapid physical dependence, and respiratory depression — breathing slowing until it stops — is the primary lethal mechanism.[2] The short half-life accelerates tolerance and interdose withdrawal; combining it with opioids dramatically amplifies respiratory depression and has been documented in multiple fatalities.

Dose and durationby route · individual sensitivity varies

Oral(µg)
Threshold< 50 µgLight75 – 200 µgCommon200 – 400 µgStrong400 – 999 µgHeavy999+ µg

Starts in 20 – 60 minLasts 6 – 10 hoursAfter-effects 6 – 24 hours

Body and dependence

Acute toxicity
High
Chronic toxicity
Moderate
Physical dependence
High
Psychological dependence
High
Withdrawal
Life-threatening · fatal · medical supervision
Compulsive redosing
High

Tolerance

Builds
Rapid
Fully resets after
10.5 days
Carries over to
benzodiazepines; Z-drugs (zolpidem, zopiclone, zaleplon); barbiturates; alcohol

Effectslikely at a common dose

Perception
none likely · 6 possible, including Spatial disorientation, Visual acuity suppression, Vestibular distortion
Body
Sedation; Muscle relaxation; +11 possible, including Motor control impairment, Dizziness, Nystagmus (eye wobbles)
Thinking
Cognitive impairment; +17 possible, including Memory suppression, Decision impairment, Analysis suppression
Feeling
Anxiety suppression; +3 possible
Self
none likely · 6 possible, including Craving, Communication suppression
Time
none likely · 2 possible, including Temporal disorientation

Who shouldn't take it

Absolute
Concurrent opioid use; Severe respiratory insufficiency; Severe hepatic impairment; Concurrent alcohol use
Relative
Myasthenia gravis; History of substance use disorder; Pregnancy; Elderly populations; Pediatric populations

Combinations60 recorded

Lethal (1)
Opioids
Dangerous (21)
Alpha-2 adrenergic receptor antagonist; Antipsychotics; Atypical antipsychotics; Benzodiazepines; Buprenorphine, Kratom; Cannabis, THC; Clonidine, Guanfacine; Gabapentin, Pregabalin; GHB, Baclofen; GHB, GBL; Local anesthetics; Naltrexone; SNRIs; Stimulants; Synthetic cannabinoids; Ibogaine; Ketamine, DXM, PCP; MAOIs; NSAIDs; Poppers (Alkyl nitrites); Poppers, Nitrates
Caution (26)
See full page: psychedex.org/substances/clonazolam
Not graded (12)
Not listed never means safe.

Seek help immediately if

  • Extreme drowsiness — can't stay awake or be roused
  • Confusion, slurred speech, severe loss of coordination
  • Slow, shallow, or irregular breathing
  • Unconsciousness / unresponsive; limp, floppy body
  • Blue lips or fingertips
  • Vomiting while sedated (choking / aspiration risk)
  • Cold, clammy skin; weak pulse

What to do

  1. Try to wake them — shout, firm sternal rub
  2. If unresponsive or breathing is impaired, call emergency services
  3. Place them in the recovery position — critical, they can choke on vomit
  4. Monitor breathing continuously; be ready to give rescue breaths / CPR
  5. Never leave them alone to "sleep it off"
  6. Do not give other drugs, stimulants, or more depressants

Most depressant overdoses resolve with airway protection, breathing support, and monitoring. The danger is respiratory depression and choking on vomit — sharply worse when combined with opioids or alcohol. GHB/GBL overdoses often involve sudden deep unconsciousness and may self-resolve, but airway protection is essential.

988 Suicide & Crisis LifelineFireside Project: 62-FIRESIDE

Version r1 · Not medical advice

References

  1. [1]
    ^Moosmann B, Auwärter V (2018) Designer Benzodiazepines: Another Class of New Psychoactive Substances. — Handbook of Experimental Pharmacology doi:10.1007/164_2018_154
  2. [2]
    ^Moore C, Hammers J, Marshall P (2022) Clonazolam Intoxication Case Report: Danger of Designer Benzodiazepines. — The American Journal of Forensic Medicine and Pathology doi:10.1097/paf.0000000000000803
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