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Bromazepam

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Collated from PsychonautWiki, TripSit, Pharmacology, DrugCentral. Where sources differ (e.g. dosing), Compare shows them side by side.

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Also known as Bromazepam, Brozam, Lectopam, Lexomil, Lexotan, Lexilium, Lexaurin, Brazepam, Rekotnil, Bromaze, Somalium, Lexatin, Calmepam, Zepam, LexotanilPW

This page has not been fully approved by the PsychonautWiki administrators. It may contain incorrect information, particularly with respect to dosage, duration, subjective effects, toxicity and other risks. It may also not meet PW style and grammar standards.PW

ToxicityPW
low toxicity; potentially lethal when mixed with depressants like alcohol or opioids

Oral

Route dataPsychonautWiki

ThresholdLightCommonStrongHeavy
1.5 mg1.5–3 mg3–6 mg6–12 mg12 mg+
015 mg
LightCommonStrongHeavy
Onset14–15 minutes
Come-up15–120 minutes
Peak2–12 hours
Offset30–60 minutes
Total6–15 hours
After-effects12–22 hours
OnsetCome-upPeakOffset

Dangerous interactionsPW

🧬 Receptor activityDC

TargetActionAffinitySource
GABA-A receptor alpha-1/beta-2/gamma-2 (GABRA1)DRUGCENTRAL
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Mechanism of actionPH

Bromazepam binds to the GABA-A receptor producing a conformational change and potentiating its inhibitory effects. Other neurotransmitters are not influenced.

PharmacodynamicsPH

Bromazepam is a lipophilic, long-acting benzodiazepine and with sedative, hypnotic, anxiolytic and skeletal muscle relaxant properties. It does not possess any antidepressant qualities. Bromazepam, like other benzodiazepines, presents a risk of abuse, misuse, and dependence. According to many psychiatric experts, Bromazepam has a greater abuse potential than other benzodiazepines because of fast resorption and rapid onset of action.

Pharmacokinetics

Half-lifePH

10-20 hours

AbsorptionPH

Bioavailability is 84% following oral administration. The time to peak plasma level is 1 - 4 hours. Bromazepam is generally well absorbed after oral administration.
Urine (69%), as metabolites
1.56 L/kg
0.82 mL/min/kg.

MetabolismPH

Hepatically, via oxidative pathways (via an enzyme belonging to the Cytochrome P450 family of enzymes). One of the main metabolites is 3-hydroxybromazepam. It is pharmacologically active and the half life is similar to that of the parent compound.
Bromazepam has known human metabolites that include 3-Hydroxybromazepam.
Hepatically, via oxidative pathways (via an enzyme belonging to the Cytochrome P450 family of enzymes). One of the main metabolites is 3-hydroxybromazepam. It is pharmacologically active and the half life is similar to that of the parent compound.
Route of Elimination: Urine (69%), as metabolites
Half Life: 10-20 hours

Protein bindingPH

70%

Plan when to take Bromazepam — see where onset, peak and comedown land on the clock

Fact-sheets from PsychonautWiki. Harm-reduction reference only — not medical advice.