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Drug reference

Modafinil

Wakefulness-promoting agent (non-amphetamine stimulant) · Central Nervous System Stimulant (non-amphetamine type), Treatment for excessive sleepiness

Also known as Modalert, Modapro, Modafin

START
200 mg PO each morning (shift-work: 1 h pre-shift)
TYPICAL MAX
400 mg/day (limited added benefit)
STOP IF
Any rash/mucosal lesion (stop immediately — SCAR risk), psychosis/mania, severe CV symptoms
WATCH
Skin/mucosa, BP/HR, mood/psychiatric symptoms, contraceptive efficacy
CDSCO approvedSchedule HATC N06BA07
Dose laddermg/d
100start200standard/day400max/day
Renal dose adjustmenteGFR mL/min/1.73m²
FULLUsual dosing30CAUTIONLimited data — use caution90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
1hONSET3hPEAK13h14hDURATION
ONSET
1h · wakefulness onset
PEAK
3h · Cmax
13h · plasma t½
DURATION
14h · daytime effect
EXCRETION
Hepatic metabolism; ~80% renal metabolites
route + CYP
INTERACTIONS
12 major
incl. contraindicated
PREGNANCY
Avoid — IUGR/possible congenital malformation signal; effective non-hormonal contraception advised
FDA category + note
Top interactionssee all 12
  • ValbenazineContraindicatedTextbookG&G 14e · p372
  • AvapritinibSevereDatabaseDDInter
  • AxitinibSevereDatabaseDDInter
  • BedaquilineSevereDatabaseDDInter
Available in India

50 branded formulations. Look up specific brands in the Drugs workspace.

Mechanism

Promotes wakefulness; primary action is weak dopamine-transporter inhibition raising synaptic dopamine, with downstream effects on orexin, histamine, noradrenaline and glutamate/GABA networks. Lower abuse potential than classical stimulants.

Indications

Excessive daytime sleepiness in narcolepsyObstructive sleep apnoea (adjunct to CPAP)Shift-work sleep disorder

Dosing

Adult
200 mg PO once each morning (OSA/narcolepsy); shift-work: 200 mg ~1 h before shift. Up to 400 mg/day (limited added benefit).
Pediatric
Not approved (paediatric SJS/TEN signal).
Renal adjustment
No established adjustment (limited data in severe impairment).
Hepatic adjustment
Severe hepatic impairment: reduce dose by ~50%.
Geriatric
Consider lower dose (reduced elimination).
Max dose
400 mg/day

Pharmacokinetics

Onset
~1 h
Peak effect
2–4 h
Duration
~12–15 h
Half-life
~12–15 h
Bioavailability
Well absorbed (absolute BA not defined; tablet)
Protein binding
~60%
Metabolism
Hepatic (amide hydrolysis; CYP3A4 minor); moderate CYP3A4 inducer, CYP2C19 inhibitor
Excretion
Renal (~80% as metabolites; <10% unchanged)

Contraindications

  • Hypersensitivity/prior rash to modafinil or armodafinil
  • Caution: significant cardiac disease (LVH, mitral valve prolapse, recent MI/unstable angina), history of psychosis

Side effects

Common
HeadacheNauseaNervousness/anxiety, insomniaDizzinessDecreased appetite
Serious
  • Severe cutaneous reactions: SJS/TEN, DRESS
  • Psychiatric: psychosis, mania, suicidal ideation
  • Hypersensitivity multi-organ reaction
  • Palpitations/tachycardia, raised BP

Pregnancy & lactation

Pregnancy

Avoid — IUGR/possible congenital malformation signal; effective non-hormonal contraception advised

Lactation

Limited data; avoid or monitor infant

Drug interactions

Valbenazine
Contraindicated
Textbook

Potential loss of valbenazine efficacy.

Not recommended.

Source: G&G 14e · p372

Avapritinib
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Axitinib
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Bedaquiline
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Benzhydrocodone
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Bosutinib
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Brigatinib
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Butorphanol
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Capmatinib
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Citalopram
Severe
Database

Drug interaction classified as: metabolism.

Source: DDInter

Cobimetinib
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Daclatasvir
Severe
Database

Clinical effect not specified

Source: DDInter

Related guidelines

Ask House about Modafinil

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: KD Tripathi 7e, Goodman & Gilman 14e, Harrison 22e, Katzung·Verified: 2026-05-19 · House clinical team·Cockpit curated: 2026-05-19