Developed as 'Ordinator' by Laboratoires Dausse in France during the 1960s for treatment of psychasthenia. Fenozolone is structurally related to pemoline and acts as a norepinephrine-dopamine releasing agent with weaker serotonin activity. Clinical imaging studies demonstrate focused sensorimotor activation comparable to fluoxetine with greater sympathetic arousal. Community reports suggest optimal doses of 15-25 mg oral for focused stimulation with minimal anxiety. Higher doses above 40 mg significantly increase cardiovascular strain and anxiety.
Fenozolonă molecular structure diagram from the DrugsPRO substance library.
Also known as: Ld-3394, Ordinator
Classification
Chemical: Aminorex
Psychoactive: Stimulant
Tag: 4-oxazolidinone
Tag: Research-Chemical
Effects
Stimulation
Increased Heart Rate
Vasoconstriction
Physical Euphoria
Stamina Enhancement
Loss Of Appetite
Focus Enhancement
Motivation Enhancement
Wakefulness
Euphoria
Anxiety
Thought Acceleration
Appetite Suppression
Light Sensitivity
Bodily Control Enhancement
Increased Libido
Increased Music Appreciation
Dehydration
Routes of Administration
Oral
Dosage
Threshold: 5 mg
Light: 5-15 mg
Common: 15-30 mg
Strong: 30-50 mg
Heavy: 50 mg
Duration
Onset: 0.25-0.75 h
Comeup: 0.5-1 h
Peak: 1-3 h
Offset: 1-2 h
After Effects: 2-12 h
Insufflated
Dosage
Threshold: 5 mg
Light: 5-10 mg
Common: 10-20 mg
Strong: 20-35 mg
Heavy: 35 mg
Duration
Onset: 0.08-0.17 h
Comeup: 0.25-0.5 h
Peak: 1-3 h
Offset: 1-2 h
After Effects: 2-12 h
Harm Reduction
Check interactions before mixing substances, pay attention to dose spacing and hydration, and treat all dosage guidance as approximate rather than guaranteed safe.
Sources
Substance data is aggregated from the following public harm-reduction and reference sources.
This static page is intended as a readable non-JS and prerender-friendly library export.
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Fenozolone - Ghid de substanțe DrugsPRO
Fenozolone: Developed as 'Ordinator' by Laboratoires Dausse in France during the 1960s for treatment of psychasthenia. Fenozolone is structurally related to pemoline and acts as a norepinephrine-dopamine releasing agent with weaker serotonin activity. Clinical imaging studies demonstrate focused sen
