Cyclazodone Facts
Stimulant;
Description
Cyclazodone is a synthetic stimulant of the oxazolidinone class. It raises dopamine and norepinephrine levels in the brain, producing the focused, wakeful drive characteristic of stimulants.[1][2]
Subjective effects include focus enhancement, motivation, improved cognitive performance, and mild mood elevation. The experience is task-oriented and context-dependent — structured work feels more absorbing, but the same dose without purposeful activity produces directionless restlessness.[3]
Dependence liability is presumed moderate; the primary toxicity concern is liver damage inherited from the pemoline class. Pemoline caused fatal liver failure in at least 21 patients,[4] and structural similarity to cyclazodone gives no reason to assume that risk is gone.[5]
Dose and durationby route · individual sensitivity varies
Starts in 20 – 45 minLasts 5 – 7 hoursAfter-effects 2 – 6 hours
Body and dependence
- Acute toxicity
- Moderate
- Chronic toxicity
- High
- Physical dependence
- Low
- Psychological dependence
- Moderate
- Withdrawal
- Mild
- Compulsive redosing
- Moderate
Tolerance
- Builds
- Moderate
- Fully resets after
- 10.5 days
- Carries over to
- amphetamine;
methylphenidate; cocaine; other dopaminergic stimulants
Effectslikely at a common dose
- Perception
- none likely · 4 possible
- Body
- Stimulation;
Appetite suppression; Pupil dilation; Wakefulness; +20 possible, including Vasoconstriction, Insomnia, Muscle tension - Thinking
- none likely · 20 possible, including Cognitive dysphoria, Compulsive redosing urge
- Feeling
- none likely · 7 possible, including Anxiety, Anhedonia, Depression
- Self
- none likely · 8 possible, including Ego inflation, Craving
Who shouldn't take it
Combinations61 recorded
Seek help immediately if
No emergency profile is recorded for this substance. Not recorded never means no risk.
988 Suicide & Crisis LifelineFireside Project: 62-FIRESIDE
References
- [1]^Docherty JR (2008) Pharmacology of stimulants prohibited by the World Anti-Doping Agency (WADA). — British Journal of Pharmacology doi:10.1038/bjp.2008.124
- [2]^Luethi D, Liechti ME (2020) Designer drugs: mechanism of action and adverse effects — Archives of Toxicology doi:10.1007/s00204-020-02693-7
- [3]
- [4]^Marotta PJ, Roberts EA (1998) Pemoline hepatotoxicity in children — The Journal of Pediatrics PMID:9602211
- [5]