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Naratriptan

Triptan · Anti-migraine agent

Also known as Naratriptan hydrochloride, Naramig

TriptanAnti-migraine agent
CDSCO approved
EXCRETION
not curated
INTERACTIONS
12 major
SEVERE in our sources
PREGNANCY
Manufacturers advise avoidance unless potential benefit outweighs risk.
FDA category + note
Top interactionssee all 12
  • AlmotriptanSevereDatabaseDDInter
  • BromocriptineSevereDatabaseDDInter
  • CabergolineSevereDatabaseDDInter
  • CitalopramSevereDatabaseDDInter

Mechanism

Naratriptan is a selective 5-HT1B/1D receptor agonist that constricts dilated meningeal blood vessels and inhibits trigeminal neuropeptide release, reversing the pathophysiology of migraine. Compared to sumatriptan, naratriptan has a longer plasma half-life (~6 hours vs 1-2 hours), higher oral bioavailability (70%), and slower onset, making it better suited for migraines with gradual onset or prolonged duration and associated with lower headache recurrence rates.

Indications

Treatment of acute migraineMenstrual migraine prophylaxis (unlicensed indication)Acute treatment of migraine

Dosing

Adult
2.5 mg orally; can be repeated after 2 hours if initial dose is inadequate.
Renal adjustment
Avoid if eGFR less than 15 mL/minute/1.73 m2. Max. 2.5 mg in 24 hours.
Hepatic adjustment
Avoid in severe impairment (no information available from manufacturer).

Contraindications

  • eGFR less than 15 mL/minute/1.73 m2
  • Severe hepatic impairment
  • Pregnancy (manufacturers advise avoidance unless potential benefit outweighs risk)
  • Ischemic heart disease
  • Coronary artery vasospasm
  • Severe renal impairment
  • Within 24 hours of another triptan
  • Within 24 hours of an ergot derivative
  • Within 24 hours of SSRIs
  • Within 24 hours of SNRIs

Side effects

Common
DrowsinessDizzinessSomnolenceNeck painChest painParesthesiasAstheniaFatigueFlushingFeelings of pressure/tightnessNauseaSweating
Serious
  • Medication-overuse headache
  • May cause fetal harm
  • Serotonin syndrome
  • Coronary artery vasospasm
  • Transient myocardial ischemia
  • Atrial arrhythmias
  • Ventricular arrhythmias
  • Myocardial infarction

Pregnancy & lactation

Pregnancy

Manufacturers advise avoidance unless potential benefit outweighs risk.

Lactation

Present in milk in animal studies; withhold breast-feeding for 24 hours.

Drug interactions

Almotriptan
Severe
Database

Clinical effect not specified

Source: DDInter

Bromocriptine
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Cabergoline
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Citalopram
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Desipramine
Severe
Database

Clinical effect not specified

Source: DDInter

Desvenlafaxine
Severe
Database

Clinical effect not specified

Source: DDInter

Dexfenfluramine
Severe
Database

Clinical effect not specified

Source: DDInter

Dihydroergotamine
Severe
Database

Clinical effect not specified

Source: DDInter

Dolasetron
Severe
Database

Clinical effect not specified

Source: DDInter

Duloxetine
Severe
Database

Clinical effect not specified

Source: DDInter

Eletriptan
Severe
Database

Clinical effect not specified

Source: DDInter

Ergometrine
Severe
Database

Clinical effect not specified

Source: DDInter

Related guidelines

Other Triptan drugs

Ask House about Naratriptan

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Sources: KD Tripathi 7e, Goodman & Gilman 14e, Katzung, BNF·Verified: 2026-05-10 · House clinical team