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BiologicalX

Comparison

DHEA vs Modafinil

Side-by-side of DHEA and Modafinil. Every row below is pulled from the compound schema and will update as our data grows. For deeper reads, follow through to each compound page.

Effects at a glance

DHEA

  • Adrenal androgen precursor; serum DHEA-S declines progressively after the third decade of life
  • OTC dietary supplement in US under DSHEA 1994; prescription in EU, UK, Canada, Australia
  • FDA approved as Intrarosa (6.5 mg vaginal insert) for postmenopausal dyspareunia in 2016
  • Acts as tissue-specific prohormone converted intracrinologically to testosterone and estrogens
  • Best evidence: adrenal insufficiency replacement and vaginal atrophy; weaker on cognition and longevity
  • WADA banned in competitive sport; banned in NCAA, MLB, NFL, IOC settings

Modafinil

  • FDA approved in 1998 for narcolepsy, with later additions for shift-work sleep disorder and OSA residual sleepiness
  • Schedule IV controlled substance in the US; prescription-only in EU, UK, Australia
  • Increases wakefulness via weak dopamine reuptake inhibition plus histaminergic, noradrenergic, and orexinergic activation
  • Long half-life of 12 to 15 hours requires morning dosing to avoid sleep disruption
  • Modest cognitive enhancement signal in non-sleep-deprived adults at 100 to 200 mg (Battleday meta-review 2015)
  • Substantial CYP3A4 induction reduces hormonal contraceptive efficacy; barrier methods recommended

Side-by-side

Attribute DHEA Modafinil
Category hormone pharmaceutical
Also known as dehydroepiandrosterone, prasterone, Intrarosa Provigil, Modalert, Modvigil, diphenylmethylsulfinyl-acetamide
Half-life (hr) 12 13
Typical dose (mg) 25 200
Dosing frequency daily, typically morning daily, morning
Routes oral, vaginal, topical oral
Onset (hr) 1 1
Peak (hr) 1 3
Molecular weight 288.42 273.35
Molecular formula C19H28O2 C15H15NO2S
Mechanism Steroid prohormone converted intracrinologically to testosterone and estrogens in target tissues; also exerts direct effects via sigma-1 receptor, GABA-A modulation, and glucocorticoid receptor interaction. Weak dopamine reuptake inhibition plus downstream activation of histaminergic, noradrenergic, and orexinergic wake-promoting systems.
Legal status OTC supplement in US (DSHEA 1994); prescription in EU, UK, Canada, Australia Schedule IV (US); prescription-only globally; not a supplement
WADA status banned banned
DEA / Rx OTC supplement in US (not scheduled); Rx in EU, UK, Canada, Australia Schedule IV
Pregnancy Contraindicated in pregnancy Not recommended
CAS 53-43-0 68693-11-8
PubChem CID 5881 4236
Wikidata Q411733 Q422968

Safety profile

DHEA

Common side effects

  • acne
  • oily skin
  • hirsutism (women)
  • gynecomastia (men, higher doses)
  • irritability
  • insomnia

Contraindications

  • hormone-sensitive cancer (breast, ovarian, prostate)
  • active liver disease
  • uncontrolled lipid disorder
  • pregnancy and lactation

Interactions

  • warfarin: case reports of altered INR; monitor(moderate)
  • estrogens (HRT): additive estrogenic effect via conversion; monitor(moderate)
  • insulin: may improve insulin sensitivity slightly; monitor glucose(minor)
  • anastrozole: may reduce DHEA-derived estrogen; clinical relevance unclear(minor)

Modafinil

Common side effects

  • headache
  • nausea
  • anxiety
  • insomnia (with late-day dosing)
  • dry mouth
  • mild blood pressure elevation

Contraindications

  • recent myocardial infarction
  • unstable angina
  • left ventricular hypertrophy
  • significant arrhythmia
  • history of Stevens-Johnson syndrome
  • psychotic disorders
  • pregnancy
  • concurrent MAOI use

Interactions

  • hormonal contraceptives: CYP3A4 induction reduces contraceptive efficacy; use barrier method(major)
  • cyclosporine: reduced cyclosporine levels via CYP3A4 induction(major)
  • warfarin: CYP2C9 inhibition raises INR(moderate)
  • phenytoin: CYP2C19 inhibition raises phenytoin levels(moderate)
  • MAOIs: potential hypertensive reaction(major)
  • classical stimulants (amphetamine, methylphenidate): additive cardiovascular and sleep-disruption effects(moderate)

Which Should You Take?

DHEA comes out ahead for most readers on the criteria we weight: 2 catalogued goals, OTC dietary supplement, oral dosing, with a Tier-A outcome catalogued. Modafinil is the right call when one of the conditionals below applies.

  • If your priority is hormonal optimization, pick DHEA.
  • If your priority is healthspan extension, pick DHEA.
  • If your priority is wakefulness, pick Modafinil.
  • If your priority is focus or working memory, pick Modafinil.

Edge case: If you want to avoid controlled substance, DHEA is the more accessible choice.

Default choice: DHEA. Lower friction to source, a Tier-A evidence outcome catalogued, and broader goal coverage. Reach for Modafinil only if your priority sits squarely in the goals it owns above.

This verdict is generated from each compound's schema (goals, legal status, evidence outcomes, dosing route). It updates automatically as our compound data evolves; the deeper read sits on each individual compound page.

Common questions

What is the difference between DHEA and Modafinil?

DHEA and Modafinil differ in category (hormone vs pharmaceutical), mechanism, and typical dosing. See the side-by-side table for full details.

Which has a longer half-life, DHEA or Modafinil?

DHEA half-life is 12 hours; Modafinil half-life is 13 hours.

Can you stack DHEA with Modafinil?

Stack compatibility depends on mechanism overlap, legal status, and individual response. Check each compound page for specific interactions and contraindications before combining.

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