Talk:Bromazolam

Revision as of 15:20, 29 August 2024 by >Zorolovesyou (general improvement of the information)

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Dosages and duration of action reported by the most reliable and up-to-date resources:

- Light dose: 0.5 mg - 1 mg - Common dose: 1 mg - 2 mg - Strong/heavy dose: 2 mg - 4 mg+ - Onset of effects (oral): 15–45 min - Duration of action: 5–8 hours

(Source: WHO Critical Review findings [1])

Fatal overdose may occur when benzodiazepines are combined with other depressants such as opiates, barbiturates, gabapentinoids, thienodiazepines, alcohol or other GABAergic substances.[2]

It is strongly discouraged to combine these substances, particularly in common to heavy doses.

Not to be confused with Flubromazolam.
Summary sheet: Bromazolam
Bromazolam
Chemical Nomenclature
Common names Bromazolam, XLI-268
Substitutive name Bromazolam
Systematic name 8-bromo-6-phenyl-1-methyl-4H-benzo[f] [1,2,4]triazolo[4,3-a] [1,4]diazepine
Class Membership
Psychoactive class Depressant
Chemical class Benzodiazepine
Routes of Administration

WARNING: Always start with lower doses due to differences between individual body weight, tolerance, metabolism, and personal sensitivity. See responsible use section.



Oral
Dosage
Threshold 0.50 mg
Light 0.5 - 1.0 mg
Common 1.0 - 2.0 mg
Strong 2.0 - 4.0 mg
Heavy 4.0 mg +
Duration
Total 6 - 20 hours [3]
Onset 15 - 45 minutes
Peak 5 - 8 hours
After effects 1 - 12 hours









DISCLAIMER: PW's dosage information is gathered from users and resources for educational purposes only. It is not a recommendation and should be verified with other sources for accuracy.


Bromazolam (also known as Brom, Bromaz, or XLI-268) is a novel depressant belonging to the benzodiazepine class. It exhibits anxiolytic, disinhibition, sedative, muscle relaxant, and memory suppression effects when administered. Bromazolam is not currently scheduled in many regions globally and is frequently distributed online as a research chemical. Structurally, it is the bromine-substituted analogue of alprazolam and has similar pharmacokinetic properties and subjective effects.

Like other benzodiazepines, Bromazolam binds to specific sites on the [[GABAA receptor]] in the brain, amplifying the inhibitory effects of gamma-aminobutyric acid (GABA).[4] Its availability on the clearnet and darknet has increased its use for self-medication and recreational purposes due to its potent effects.

It is important to note that the pharmacological properties stated are assumed based on its structure and user reports, as no extensive formal research has been conducted.

The sudden discontinuation of benzodiazepines after prolonged use can lead to severe withdrawal symptoms, including seizures or death.[5] Users are strongly advised to taper their dosage gradually rather than stopping abruptly.[6]

For guidelines on properly formatting a substance article, refer to the Content Style Guide - Substance document.

History and Culture

Bromazolam (XLI-268) is a triazolobenzodiazepine (TBZD) first synthesized in 1976 by Hoffman-La Roche. Although initially developed as a potential medication, it was never approved for use and remained unmarketed.[7] Bromazolam was first identified in Sweden in 2016 by the EMCDDA and has since been found in nine countries, including Australia, Austria, China, Finland, Germany, India, Sweden, the UK, and the USA.

In European markets, Bromazolam is often sold as blue Diazepam pills,[8] while in the United States, it is more commonly sold as Alprazolam.

Chemistry

 
Chemical structural comparison of Alprazolam and Bromazolam by Kevin G. Shanks (2023).

Bromazolam is a chemical analog of alprazolam, where the chlorine atom in alprazolam is replaced by a bromine atom.

Pharmacology

Bromazolam is a triazolobenzodiazepine (TBZD) and was synthesized in 1976, though it was not brought to market.[9] It acts as a non-subtype selective agonist at the benzodiazepine (BZD) site of [[GABAA receptors]], with a binding affinity of 2.81nM at the α1 subtype, 0.69nM at α2, and 0.62nM at α5.[10] Benzodiazepines enhance the efficiency of GABA neurotransmission, producing sedating and anxiolytic effects[11].

The GABAA receptor consists of five subunits out of a possible 19, leading to a wide variety of receptor subtypes with different properties and interactions with benzodiazepines. Triazolobenzodiazepines like Bromazolam may also possess antidepressant properties, potentially due to their chemical similarity to tricyclic antidepressants.[12]

Subjective Effects

 
This subjective effects section is a stub.

As such, it is still in progress and may contain incomplete or wrong information.

You can help by expanding or correcting it.

Bromazolam's subjective effects include sedation, relaxation, anxiety suppression, and decreased inhibition.

Disclaimer: The effects listed below cite the Subjective Effect Index (SEI), an open research literature based on anecdotal user reports and the personal analyses of PsychonautWiki contributors. As a result, they should be viewed with a healthy degree of skepticism.

It is also worth noting that these effects will not necessarily occur in a predictable or reliable manner, although higher doses are more liable to induce the full spectrum of effects. Likewise, adverse effects become increasingly likely with higher doses and may include addiction, severe injury, or death ☠.

Physical effects
 

Visual effects
 

Cognitive effects
 


Experience Reports

There are currently 0 experience reports available in our experience index.

Additional experience reports for Bromazolam can be found here:

Toxicity and Harm Potential

 

This toxicity and harm potential section is a stub.

As a result, it may contain incomplete or even dangerously wrong information! You can help by expanding upon or correcting it.
Note: Always conduct independent research and use harm reduction practices if using this substance.

It is strongly recommended to employ harm reduction practices while using this substance.

Tolerance and Addiction Potential

Long-term use of Bromazolam can lead to tolerance, physical dependence, and withdrawal symptoms associated with benzodiazepines, including the potential for life-threatening withdrawal seizures.

Dangerous Interactions

Like other benzodiazepines, Bromazolam should not be mixed with alcohol or other central nervous system depressants due to the high risk of fatal overdose caused by respiratory depression.

 

This dangerous interactions section is a stub.

As such, it may contain incomplete or invalid information. You can help by expanding upon or correcting it.

Warning: Many psychoactive substances that are reasonably safe to use on their own can suddenly become dangerous and even life-threatening when combined with certain other substances. The following list provides some known dangerous interactions (although it is not guaranteed to include all of them).

Always conduct independent research (e.g. Google, DuckDuckGo, PubMed) to ensure that a combination of two or more substances is safe to consume. Some of the listed interactions have been sourced from TripSit.

Bromazolam is currently unscheduled in many countries, though some states and nations have specific controls:

- **United Kingdom:** Classified as a Class C controlled substance.[14] - **United States:** Federally unscheduled, though state-level regulations like in Virginia have placed Bromazolam into Schedule I.[15]. - **Canada:** Classified as a Schedule IV controlled substance. - **Germany:** Subject to national control legislation.

See Also

Literature

  • APA formatted references

Refer to the citation formatting guide for help in properly formatting citations.

References

  1. WHO Critical Review Report: Bromazolam (2022)
  2. Risks of Combining Depressants - TripSit 
  3. WHO Critical Review Report: Bromazolam (2022)
  4. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303399/
  5. A fatal case of benzodiazepine withdrawal. (PubMed.gov / NCBI) | http://www.ncbi.nlm.nih.gov/pubmed/19465812
  6. Canadian Guideline for Safe and Effective Use of Opioids for Chronic Non-Cancer Pain - Appendix B-6: Benzodiazepine Tapering | http://nationalpaincentre.mcmaster.ca/opioid/cgop_b_app_b06.html
  7. Manchester KR, Lomas EC, Waters L, Dempsey FC, Maskell PD (January 2018). "The emergence of new psychoactive substance (NPS) benzodiazepines: A review". Drug Testing and Analysis. 10 (1): 37–53. doi:10.1002/dta.2211. PMID 28471096.
  8. https://www.wedinos.org/sample-results
  9. Manchester KR, Lomas EC, Waters L, Dempsey FC, Maskell PD (January 2018). "The emergence of new psychoactive substance (NPS) benzodiazepines: A review". Drug Testing and Analysis. 10 (1): 37–53. doi:10.1002/dta.2211. PMID 28471096.
  10. Benzodiazepine interactions with GABA receptors (PubMed.gov / NCBI) | http://www.ncbi.nlm.nih.gov/pubmed/6147796
  11. http://www.ncbi.nlm.nih.gov/pubmed/2450203
  12. Barbee JG (October 1993). "Memory, benzodiazepines, and anxiety: integration of theoretical and clinical perspectives". The Journal of Clinical Psychiatry. 54 Suppl (Suppl): 86–97, discussion 98–101. PMID 8262893.
  13. Goyal, Sarita. "Drugs and Dreams." Indian Journal of Clinical Practice (n.d.): n. pag. Web. | http://medind.nic.in/iaa/t13/i3/iaat13i3p624.pdf
  14. https://publichealthscotland.scot/publications/rapid-action-drug-alerts-and-response-radar-alerts/radar-bromazolam-alert-2023/legal-status/#:~:text=In%20the%20UK%2C%20many%20benzodiazepines,be%20due%20to%20international%20control.
  15. https://web.archive.org/web/20230323012949/https://law.lis.virginia.gov/vacode/title54.1/chapter34/section54.1-3446/
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