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Nimetazepam

Nimetazepam molecule structureNimetazepam molecule structure
1-Methylnitrazepam
Erimin, Erimin-5, Happy 5, Lavol, Ro 5-3453Open in Piru
Chemical Class

Nimetazepam is an intermediate-acting benzodiazepine depressant with strong sedative, sleep-inducing and anxiety-reducing effects. It was first synthesized by a team at Hoffmann-La Roche in 1964. It also has muscle-relaxant properties1 and particularly potent anticonvulsant effects, and has been prescribed for severe insomnia. Its use can lead to addiction.2 In Malaysia, many tablets sold as nimetazepam on the illicit market are counterfeit,3 with other benzodiazepines, including diazepam and nitrazepam, sometimes sold in its place.4

Dosage & Duration

Dosage

Doses are population estimates that vary widely between individuals.

Threshold~2.5 mg
Light2.5-5 mg
Moderate5-10 mg
Strong10-20 mg
Heavy20+ mg

Duration

Onset15-30 minutes
After Effects12-24 hours
Total5-8 hours

Subjective Effects

Subjective Effects not written up yet

Reagent Testing

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

Marquis(MQ)
No reaction
No reaction
Mecke(ME)
No reaction
No reaction
Mandelin(MD)
No reaction
No reaction
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Pharmacology

Pharmacokinetics

Nimetazepam is rapidly absorbed after oral administration, with nearly complete absorption from the gut and very good bioavailability. Blood concentrations of the parent drug decline in two phases, with an initial half-life of 0.5-0.7 hours and a terminal elimination half-life of 8-26.5 hours (mean 17.25 hours). It is partially converted to a metabolite with a long elimination half-life, which contributes to accumulation with repeated administration.

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 not written up yet

Harm Potential

Addiction & Dependence

Psychological

Nimetazepam has habit-forming properties and substantial misuse and addiction among medical and non-medical users. High binding affinity, high potency, rapid onset, and short-to-intermediate action contribute to its abuse potential.

Physical

Nimetazepam can cause physical dependence and a withdrawal syndrome, which contribute to its addictive potential.

Toxicity

Fetal development

In rats given 100 mg/kg, nimetazepam caused greater fetal damage than other benzodiazepines in the comparison; nitrazepam showed a similar comparative finding.5

Liver

High-dose nimetazepam exposure in rats produced slight liver enlargement at weeks 4 and 12, without histopathological changes.

Adrenal glands

High-dose nimetazepam exposure in rats produced slight adrenal enlargement at weeks 4 and 12, without histopathological changes.

Testes

High-dose nimetazepam exposure in rats produced testicular atrophy at weeks 4 and 12, with degeneration of the seminiferous epithelium.

Ovaries

High-dose nimetazepam exposure in rats produced ovarian atrophy at weeks 4 and 12, without histopathological changes.

History & Culture

Nimetazepam was first synthesized in 1964 by a team at Hoffmann-La Roche. The Japanese corporation Sumitomo manufactured and marketed it under the brand name Erimin. During the 1980s and 1990s, it was widely prescribed for severe insomnia in Japan, Malaysia, Brunei, the Philippines, Thailand,…

Legality

International

Controlled internationally under the UN Convention on Psychotropic Substances 1971.

By Country

Illegal1
Hong Kong flagHong KongIllegal
Controlled / restricted1
United States flagUnited Statescategorized Schedule IV FDA and DEA
Prescription1
Singapore flagSingaporePrescription only

References

Source Pages

  1. Erowid: Nimetazepam Vault
  2. TripSit Factsheet: Nimetazepam
  3. TripSit Wiki: Uncommon Benzodiazepines
  4. TripSit: Drug Combinations Wiki
  5. Wikipedia

Citations

  1. Toxicological analysis on forensic investigation in drug related cases; pharmacological information on 88 psychoactive substances in “Narcotics and Psychotropics Control Act” in Japan. Medical Mass Spectrometry (2022). https://www.jstage.jst.go.jp/article/mms/6/1/6_2022.06.007/_pdf/-char/en1
  2. Singapore Medical Council v Dr Chia Kiat Swan — Grounds of Decision. Singapore Medical Council (2019). https://isomer-user-content.by.gov.sg/77/3fe864e9-54f7-418f-96fd-40b8112a1bd7/grounds-of-decision-(190325)---dr-chia-kiat-swan.pdf1
  3. Detection of phenazepam in illicitly manufactured Erimin 5 tablets. Drug Testing and Analysis (2016). https://doi.org/10.1002/dta.19811
  4. The Quantitation of Nimetazepam in Erimin-5 Tablets and Powders by Reverse-Phase HPLC. Microgram Journal (2004). https://forendex.southernforensic.org/uploads/references/MicrogramJournal/2.1-4.27.33.pdf1
  5. Fetal toxicity of benzodiazepines in rats. PubMed (1984). https://pubmed.ncbi.nlm.nih.gov/61512221
  6. ACMT 2018 Annual Scientific Meeting Abstracts—Washington, DC. Journal of Medical Toxicology (2018). https://doi.org/10.1007/s13181-018-0655-712
  7. Department of Justice, Hong Kong e-Legislation — Cap. 134 Dangerous Drugs Ordinance (current English XML, 12 June 2026). resource.data.one.gov.hk (n.d.). https://resource.data.one.gov.hk/doj/data/hkel_c_leg_cap_1_cap_300_en.zip1
  8. Misuse of Drugs Act 1973 — First Schedule, Part 3 (Class C Drugs). sso.agc.gov.sg (n.d.). https://sso.agc.gov.sg/Act/MDA1973?Phrase=class%20c&ProvIds=Sc1-&ViewType=Within&WiAl=11
  9. Misuse of Drugs Regulations — regulations 6 to 12 and Second Schedule. sso.agc.gov.sg (n.d.). https://sso.agc.gov.sg/SL/MDA1973-RG1?WholeDoc=11
  10. Nimetazepam | Central Narcotics Bureau. cnb.gov.sg (n.d.). https://www.cnb.gov.sg/singapore-drug-situation/drugs--psychoactive-substances--and-inhalants/nimetazepam/1

Further Reading

  1. ChemSpider: Nimetazepam Chemical Structure
  2. Know Your Stuff NZ: TripSit Drug Interaction Chart

Article Status

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