Adrafinil
NOOTROPICAlso known as: CRL-40028, Olmifon
What is Adrafinil?
Adrafinil is a prodrug of modafinil, a DEA Schedule IV controlled substance. It requires hepatic metabolism to produce the active drug, placing significant strain on the liver. Selling adrafinil has resulted in criminal prosecution and prison time for supplement sellers.
Why is Adrafinil Banned?
Prodrug of DEA Schedule IV controlled substance (modafinil). Classified as unapproved new drug by FDA. Hepatotoxic. Active criminal enforcement with prison sentences.
Health Risks & Side Effects
Health Risk Level
This substance has a moderate risk of overdose and low addiction potential.
warningCommon Side Effects
- arrow_rightLiver toxicity
- arrow_rightElevated liver enzymes
- arrow_rightInsomnia
- arrow_rightAnxiety
- arrow_rightHeadache
- arrow_rightNausea
blockContraindications
- arrow_rightLiver disease
- arrow_rightHeart conditions
- arrow_rightSeizure disorders
- arrow_rightPregnancy
- arrow_rightOther hepatotoxic drugs
How Does Adrafinil Work?
Metabolized by the liver into modafinil (Schedule IV). Increases dopamine and norepinephrine neurotransmission, promoting wakefulness. Hepatotoxic due to extensive first-pass metabolism required for activation.
History
Developed in France in the 1970s by Lafon Laboratories for narcolepsy treatment. Voluntarily discontinued in France in 2011 due to liver risks and availability of modafinil. US supplement sellers prosecuted criminally in 2023.
verified_userSafe Legal Alternatives
Don't risk your health with Adrafinil. Here are proven, legal alternatives that provide similar benefits safely:
No alternatives available at this time. Check back soon.
Learn More
Research articles and educational resources
Overview
Adrafinil
Adrafinil, sold under the brand name Olmifon, is a wakefulness-promoting medication that was formerly used in France to improve alertness, attention, wakefulness, and mood, particularly in the elderly. It was also used off-label by individuals who wished to avoid fatigue, such as night workers or others who needed to stay awake and alert for long periods of time. Additionally, the medication has been used non-medically as a novel vigilance-promoting agent.
Scientific Research
From PubMed • 3 peer-reviewed studies
Pharmacokinetic and pharmacodynamic of the cognitive enhancer modafinil: Relevant clinical and forensic aspects.
Modafinil is a nonamphetamine nootropic drug with an increasingly therapeutic interest due to its different sites of action and behavioral effects in comparison to cocaine or amphetamine. A review of modafinil (and of its prodrug adrafinil and its R-enantiomer armodafinil) chemical, pharmacokinetic, pharmacodynamic, toxicological, clinical and forensic aspects was performed, aiming to better understand possible health problems associated to its unconscious and unruled use. Modafinil is a racemate metabolized mainly in the liver into its inactive acid and sulfone metabolites, which undergo primarily renal excretion. Although not fully clarified, major effects seem to be associated to inhibition of dopamine reuptake and modulation of several other neurochemical pathways, namely noradrenergic, serotoninergic, orexinergic, histaminergic, glutamatergic and GABAergic. Due its wake-promoting effects, modafinil is used for the treatment of daily sleepiness associated to narcolepsy, obstructive sleep apnea and shift work sleep disorder. Its psychotropic and cognitive effects are also attractive in several other pathologies and conditions that affect sleep structure, induce fatigue and lethargy, and impair cognitive abilities. Additionally, in health subjects, including students, modafinil is being used off-label to overcome sleepiness, increase concentration and improve cognitive potential. The most common adverse effects associated to modafinil intake are headache, insomnia, anxiety, diarrhea, dry mouth and raise in blood pressure and heart rate. Infrequently, severe dermatologic effects in children, including maculopapular and morbilliform rash, erythema multiforme and Stevens-Johnson Syndrome have been reported. Intoxication and dependence associated to modafinil are uncommon. Further research on effects and health implications of modafinil and its analogs is steel needed to create evidence-based policies.
[Spironolactone-induced pemphigoid].
Sporadic observations would suggest that certain drugs play a role in the development of pemphigoid. A recent case-control study on long-term drug use associated with pemphigoid was unable to confirm the suspected role of these drugs, but did demonstrate a significant association between the development of pemphigoid and use of spironolactone.
Adrafinil-induced orofacial dyskinesia.
We describe the first case of orofacial abnormal movements induced by adrafinil, a vigilance promoting agent of the same pharmacological class as modafinil. The dyskinesias did not spontaneously recover despite adrafinil withdrawal for a 4-month period. They were secondly dramatically improved by tetrabenazine, a presynaptic dopaminergic depleting drug which was introduced after the 4-month adrafinil-free period.