Warning
This is an unofficial archive of PsychonautWiki as of 2025-08-08T03:33:20Z. Content on this page may be outdated, incomplete, or inaccurate. Please refer to the original page for the most up-to-date information.

Galantamine

From PsychonautWiki Archive
Revision as of 15:45, 10 July 2016 by >Catharsis (Created page with "{| |- | {{proofread}} || {{approval}} |} {{SubstanceBox/Galantamine}} {| |- |- | ''Summary sheet: Galantamine'' |} '''Galantamine (Nivalin, Razadyne, R...")
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search

Template:Proofread

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.

Galantamine
Chemical Nomenclature
Common names Galantamine
Systematic name (4aS,6R,8aS)-5,6,9,10,11,12-Hexahydro-3-methoxy-11-methyl-4aH-[1]benzofuro[3a,3,2-ef][2]benzazepin-6-ol
Class Membership
Psychoactive class Nootropic / Oneirogen
Chemical class Benzazepine
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
Bioavailability 90%[1]
Threshold 1 mg
Light 4 - 8 mg
Common 8 - 16 mg
Strong 16 - 24 mg
Heavy 24 mg +
Duration
Total 6 - 12 hours
Onset 20 - 60 minutes









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.

Interactions
Summary sheet: Galantamine

Galantamine (Nivalin, Razadyne, Razadyne ER, Reminyl, Lycoremine) is a water soluble is a reversible, competitive acetylcholinesterase inhibitor. It is an alkaloid that is obtained synthetically or from the bulbs and flowers of Galanthus caucasicus, Galanthus woronowii and related genera.[2]

Studies of usage in modern medicine began in the Soviet Union in the 1950s by Soviet pharmacologists M. D. Mashkovsky and R. P. Kruglikova–Lvova.[3] The active ingredient was extracted, identified, and studied, particularly in relation to its mechanism of action. Galantamine has been used for decades in Eastern Europe and Russia for various indications such as treatment of myasthenia, myopathy, and sensory and motor dysfunction associated with disorders of the central nervous system. In the US, it is FDA approved for the treatment of Alzheimer's disease.[4]

It is available in both a prescription form and as an over the counter supplement.

More recently, Galantamine has been popularized in supplement groups for it's ability to improve dream recall and induce lucid dreaming. It is best taken 30 minutes to one hour before bed. Galantamine has a wide range of unpleasant side effects related to digestion, but this may be mitigated by dosing sublingually, rather than orally.


Chemistry

This chemistry section is incomplete.

You can help by adding to it.

It has an empirical formula of C17H21NO3 •HBr and a molecular weight of 368.27.

Pharmacology

Galantamine, a tertiary alkaloid, is a competitive and reversible inhibitor of acetylcholinesterase. Is postulated to exert its therapeutic effect by enhancing cholinergic function. This is accomplished by increasing the concentration of acetylcholine through inhibiting acetylcholinesterase, a neurochemical responsible for breaking down acetylcholine. Higher concentrations of acetylcholine have been linked to higher levels of cognition and focus.

Subjective effects

The effects listed below are based upon the subjective effects index and personal experiences of PsychonautWiki contributors. The listed effects will rarely (if ever) occur all at once, but heavier dosages will increase the chances and are more likely to induce a full range of effects.

Physical effects

Cognitive effects

Visual effects

Distortions

Toxicity and harm potential

Galantamine is non-addictive, is not known to cause harm in reasonable doses, and has an extremely low toxicity relative to dose. Various studies have shown that in reasonable doses in a careful context, it presents few negative cognitive, psychiatric or toxic physical consequences, though some exist.

It is strongly recommended that one be familiar with harm reduction practices when using this drug.

Tolerance and addiction potential

Galantamine is not known to be not habit-forming and the desire to use it can actually decrease with use. It is most often self-regulating.

Galantamine does not seem to build up an immediate tolerance, and, due to its long half life, becomes stronger with prolonged use. Caution should be heeded when taking Galantamine for extended periods longer than two weeks. Galantamine presents cross-tolerance with no other known compounds, meaning that after the consumption of Galantamine all other psychoactive compounds will not have a reduced effect.

See also

References