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

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Also known as albego, limpidon, paxorTS

A benzodiazepine drug that is stronger in terms of anxiety relief than it is in terms of how hypnotic it is. It is a metabolite of diazepam and has limited anticonvulsant properties.TS

Oral

Route dataTripSit

ThresholdLightCommonStrongHeavy
10–20 mg20–40 mg—+
040 mg
LightCommonStrongHeavy
Onset45–90 minutes
Total8–12 hours
After-effects1–12 hours
OnsetCome-upPeakOffset

Mechanism of actionPH

Camazepam has been shown to bind competitively to benzodiazepine receptors in the brain with a relatively low affinity in animal models. This binding of benzodiazepine receptors by camazepam and its active metabolites is responsible for its anticonvulsant effects. Notably, only three metabolites were shown to exert anticonvulsant activity, temazepam, oxazepam, and hydroxy camazepam. The anxiolytic properties of camazepam are also attributed to their ability to bind benzodiazepine receptors, also known as GABA receptors. When benzodiazepines bind to GABA receptors they increase the efficiency with which the inhibitory neurotransmitter GABA binds.

Pharmacokinetics

AbsorptionPH

Almost completely absorbed into the bloodstream after oral administration. 90% bioavailability can be achieved in humans.
Renally eliminated.

MetabolismPH

Metabolized by the liver into more than 10 metabolites, some of which are also active and posses anticonvulsant properties. [3] One active metabolite of note is temazepam which has roughly equal in effectiveness as an anxiolytic, but is less anticonvulsant, sedating, and motor-impairing. Camazepam undergoes enantioselective metabolism by human liver microsomes. [1]
Metabolized by the liver into more than 10 metabolites, some of which are also active and posses anticonvulsant properties. [3] One active metabolite of note is temazepam which has roughly equal in effectiveness as an anxiolytic, but is less anticonvulsant, sedating, and motor-impairing.
Camazepam undergoes enantioselective metabolism by human liver microsomes. [1]
Route of Elimination: Renally eliminated.

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

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