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Metizolam Facts

Depressant; Anxiolytic; Thienodiazepine; GABA-A receptor positive allosteric modulator

Description

Metizolam (desmethyletizolam) is a synthetic depressant of the thienotriazolodiazepine class. It amplifies the brain's primary calming signal — GABA — producing sedation, reduced anxiety, and muscle relaxation.

Subjective effects include sedation, anxiety suppression, muscle relaxation, memory gaps, and reduced mental sharpness. The experience is defined by what disappears — tension, anxiety, and edge — rather than any arrival of pleasure, and is less euphoric than most designer benzodiazepines.[1]

Metizolam can cause physical dependence with repeated use; taken alone, fatal overdose is rare.[2][3] The dominant danger is combination with opioids, alcohol, or other depressants — together they suppress breathing in ways that can kill, and standard hospital screens may not detect metizolam.[4]

Dose and durationby route · individual sensitivity varies

Oral(mg)
Threshold< 0.5 mgLight1 – 2 mgCommon2 – 4 mgStrong4 – 6 mgHeavy6+ mg

Starts in 30 – 90 minLasts 5 – 8 hoursAfter-effects 10 – 30 hours

Body and dependence

Acute toxicity
Low
Chronic toxicity
Moderate
Physical dependence
High
Psychological dependence
Moderate
Withdrawal
Severe · fatal · medical supervision
Compulsive redosing
Moderate

Tolerance

Builds
Rapid
Fully resets after
10 days
Carries over to
benzodiazepines; thienodiazepines; zolpidem; zopiclone; zaleplon

Effectslikely at a common dose

Perception
none likely · 5 possible, including Visual acuity suppression, Vestibular distortion, Double vision
Body
Muscle relaxation; Sedation; +7 possible, including Motor control impairment, Dizziness, Nystagmus (eye wobbles)
Thinking
none likely · 18 possible, including Cognitive impairment, Information processing suppression, Memory suppression
Feeling
Anxiety suppression; +2 possible
Self
none likely · 6 possible, including Communication suppression, Craving
Time
none likely · 1 possible, including Temporal disorientation

Who shouldn't take it

Absolute
Concurrent opioid use; Concurrent alcohol intoxication; Respiratory insufficiency
Relative
Myasthenia gravis; History of substance use disorder; Severe hepatic impairment; Pregnancy

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/metizolam
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]
    ^El Balkhi S, Monchaud C, Herault F, Geniaux H, Saint-Marcoux F (2020) Designer benzodiazepines' pharmacological effects and potencies: How to find the information — Journal of Psychopharmacology doi:10.1177/0269881119901096
  2. [2]
    ^Brunetti P, Giorgetti R, Tagliabracci A, Huestis MA, Busardò FP (2021) Designer Benzodiazepines: A Review of Toxicology and Public Health Risks — Pharmaceuticals doi:10.3390/ph14060560
  3. [3]
    ^Greenblatt HK, Greenblatt DJ (2019) Designer Benzodiazepines: A Review of Published Data and Public Health Significance — Clinical Pharmacology in Drug Development doi:10.1002/cpdd.667
  4. [4]
    ^Manchester KR, Lomas EC, Waters L, Dempsey FC, Maskell PD (2018) The emergence of new psychoactive substance (NPS) benzodiazepines: A review. — Drug testing and analysis doi:10.1002/dta.2211
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