Product image of Naramig (Naratriptan Hydrochloride) supplied by GNH India

Naramig

Active Ingredient:
Naratriptan Hydrochloride
Origin:
EU

Naramig (Naratriptan Hydrochloride)

Naratriptan Hydrochloride, the active ingredient in Naramig, is a selective serotonin 5‑HT1B/1D receptor agonist (triptan) presented as an oral tablet for oral use. It is indicated for the acute treatment of migraine attacks in adults. Naramig is marketed in the European Union and meets the quality standards required for prescription medicines.

GNH India supplies Naramig as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Glaxosmithkline Gmbh & Co. Kg

1
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Indications & Clinical Uses

Naratriptan Hydrochloride belongs to the triptan class and is used to treat acute migraine episodes.

  • Migraine without aura: provides rapid relief of headache and associated symptoms.
  • Migraine with aura: helps abort attacks after the onset of visual or sensory disturbances.
  • Acute migraine attack: reduces pain intensity and improves functional ability during an episode.

How It Works

  • Naratriptan Hydrochloride acts as an agonist at 5‑HT1B and 5‑HT1D receptors located on intracranial blood vessels and trigeminal nerve endings. Activation of these receptors causes cranial vasoconstriction and inhibits the release of pro‑inflammatory neuropeptides, thereby terminating the cascade that generates migraine pain.

Side Effects

Common side effects are generally mild and transient, while serious or rare reactions require immediate medical attention.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Dizziness: sensation of light‑headedness.
  • Fatigue: feeling unusually tired.
  • Dry mouth: reduced salivation.
  • Tingling or numbness: usually in the extremities.
  • Flushing: warm sensation and reddening of the skin.

Serious or Rare Side Effects

  • Chest pain or tightness: possible cardiac ischemia.
  • Serotonin syndrome: agitation, hyperthermia, tremor.
  • Severe hypertension: sudden increase in blood pressure.
  • Allergic reaction: rash, itching, swelling, or difficulty breathing.
  • Ischemic colitis: abdominal pain with blood in stool.
  • Persistent visual disturbances: prolonged aura symptoms.

Precautions & Warnings

Before prescribing Naramig, clinicians should evaluate patient history and comorbid conditions.

  • Cardiovascular assessment: avoid in patients with uncontrolled hypertension, coronary artery disease, or history of stroke.
  • Drug history review: caution with other serotonergic agents to reduce serotonin syndrome risk.
  • Pregnancy considerations: safety not established; use only if potential benefit outweighs risk.
  • Breastfeeding: limited data; weigh benefits against possible infant exposure.
  • Renal or hepatic impairment: adjust use based on clinical judgment.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Naratriptan Hydrochloride can interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • MAO inhibitors: increased risk of serotonin syndrome.
  • SSRIs, SNRIs, or other serotonergic antidepressants: heightened serotonin toxicity.
  • Ergot alkaloids or other triptans: additive vasoconstriction leading to cardiovascular events.
  • Certain antihypertensives (e.g., propranolol): may elevate naratriptan plasma levels.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): may increase drug exposure.
  • CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce efficacy.
  • Diuretics: monitor blood pressure changes.
  • Antihistamines: may enhance dizziness or sedation.

Frequently Asked Questions

Naramig contains naratriptan hydrochloride, a triptan medication indicated for the acute treatment of migraine attacks in adults. It helps to relieve headache pain and associated symptoms such as nausea, photophobia, and phonophobia when taken at the onset of an attack.

Naratriptan hydrochloride works by stimulating 5‑HT1B and 5‑HT1D receptors on cranial blood vessels and trigeminal nerve endings. This causes vasoconstriction of dilated intracranial vessels and blocks the release of inflammatory neuropeptides, interrupting the migraine cascade.

The specific dose of Naramig is determined by the prescribing healthcare professional based on the individual’s medical condition, response to therapy, and other factors. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for naratriptan during pregnancy and lactation are limited. It should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision should be made in consultation with a qualified healthcare provider.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details, and any necessary import documentation.

Naramig (naratriptan) is a second‑generation triptan with a longer half‑life than some alternatives like sumatriptan, offering sustained relief for longer migraine attacks. It generally has a lower incidence of cardiovascular side effects compared with earlier triptans, but individual response varies.

Naramig tablets should be stored at ambient temperature, below 25 °C. Keep them in the original blister pack, protect from moisture and direct sunlight, and keep out of reach of children.

Naramig is taken orally as a tablet. It should be swallowed whole with a glass of water at the first sign of a migraine attack. Do not crush, chew, or split the tablet unless specifically instructed by a healthcare professional.

Serious risks include chest pain or tightness indicating possible cardiac ischemia, serotonin syndrome when combined with other serotonergic drugs, severe hypertension, and rare allergic reactions such as anaphylaxis. Patients should seek immediate medical attention if these symptoms occur.

Naramig should be avoided in patients with uncontrolled hypertension, recent myocardial infarction, severe coronary artery disease, history of stroke, or known hypersensitivity to naratriptan or any tablet excipients. It is also contraindicated when used with MAO inhibitors or other triptans.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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