Product image of Nomigrin (Naproxen Sodium, Sumatriptan Succinate) supplied by GNH India

Nomigrin

Active Ingredient:
Naproxen Sodium, Sumatriptan Succinate
Origin:
EU

Nomigrin (Naproxen Sodium, Sumatriptan Succinate)

Naproxen sodium and sumatriptan succinate, the active ingredients in Nomigrin, are an NSAID and a selective 5‑HT1B/1D receptor agonist presented as oral tablets for systemic use. The combination is indicated for the acute treatment of migraine attacks in adult patients.

GNH India supplies Nomigrin as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The product is manufactured to EU standards and distributed under strict quality controls to meet global regulatory requirements, ensuring consistent potency and safety for patients.

Manufacturer / TM Owner

Orion Corporation

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Indications & Clinical Uses

Nomigrin is used for the acute management of migraine, a neurovascular headache disorder.

  • Migraine attack: rapid relief of moderate to severe headache pain.
  • Migraine with aura: reduction of visual and sensory disturbances associated with the attack.
  • Acute episodic migraine: alleviation of accompanying nausea, photophobia and phonophobia.

How It Works

  • Sumatriptan binds selectively to 5‑HT1B and 5‑HT1D receptors on cranial blood vessels and trigeminal nerve endings, causing vasoconstriction and inhibition of neuropeptide release. Naproxen sodium inhibits cyclo‑oxygenase enzymes, decreasing prostaglandin synthesis and inflammation. The dual action provides synergistic reduction of migraine pain and associated inflammatory processes.

Side Effects

Nomigrin may cause a range of adverse reactions. The most frequently reported events are generally mild and transient.

Common Side Effects

  • Nausea: mild to moderate upset stomach.
  • Dizziness: sensation of light‑headedness.
  • Tingling or paresthesia: often in the face or extremities.
  • Chest discomfort: pressure or tightness.
  • Dry mouth: reduced salivation.
  • Fatigue: feeling unusually tired.

Serious or Rare Side Effects

  • Coronary vasospasm: chest pain with possible cardiac ischemia.
  • Serotonin syndrome: agitation, hyperthermia, muscle rigidity.
  • Severe allergic reaction: rash, swelling, anaphylaxis.
  • Hypertension: sudden increase in blood pressure.
  • Gastrointestinal bleeding: black stools or vomiting blood.
  • Stroke or transient ischemic attack: neurological deficits.

Precautions & Warnings

Before prescribing Nomigrin, clinicians should evaluate patient‑specific risk factors and monitor for potential complications.

  • Cardiovascular assessment: avoid in patients with uncontrolled coronary artery disease.
  • Drug interaction review: contraindicated with MAO inhibitors and other triptans.
  • Hepatic function: use caution in moderate to severe liver impairment.
  • Serotonin syndrome monitoring: be vigilant when combined with serotonergic agents.
  • Hypersensitivity check: discontinue if signs of allergic reaction appear.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nomigrin can interact with several medication classes; awareness of major and moderate interactions helps prevent adverse outcomes.

Major Interactions (Avoid)

  • MAO inhibitors: risk of severe hypertension and serotonin syndrome.
  • Other triptans or ergot derivatives: additive vasoconstriction.
  • SSRIs/SNRIs: increased potential for serotonin syndrome.
  • Potent CYP2C9 inhibitors (e.g., fluconazole): may raise naproxen levels.
  • Uncontrolled hypertension agents: exacerbate blood pressure spikes.

Moderate Interactions (Monitor Closely):\n- Antihypertensives: possible reduction in blood pressure control.

  • Anticoagulants/antiplatelet drugs: heightened bleeding risk.
  • Diuretics: may affect renal clearance of naproxen.
  • Other NSAIDs: increased gastrointestinal toxicity.
  • CYP3A4 inducers (e.g., rifampin): may lower sumatriptan exposure.

Frequently Asked Questions

Nomigrin is a prescription oral tablet that combines naproxen sodium and sumatriptan succinate for the acute treatment of migraine attacks in adult patients. The dual‑action formulation targets both vascular and inflammatory components of migraine, providing faster pain relief and symptom control.

Sumatriptan selectively activates 5‑HT1B/1D receptors, causing cranial vasoconstriction and blocking release of pain‑triggering neuropeptides. Naproxen sodium inhibits cyclo‑oxygenase enzymes, reducing prostaglandin production and inflammation. Together they deliver synergistic relief by addressing both vascular constriction and inflammatory pain pathways.

The specific dose and dosing schedule of Nomigrin are determined by the prescribing clinician based on individual patient needs, severity of migraine, and medical history. Patients should follow the prescriber’s instructions and not adjust the dose without medical advice.

Safety data for naproxen sodium and sumatriptan during pregnancy or lactation are limited. The medication should only be used if the potential benefit justifies the potential risk to the fetus or infant, and this decision must be made by a qualified healthcare professional.

To request Nomigrin, 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 required import documentation.

Compared with single‑agent triptans, Nomigrin adds an NSAID (naproxen) that can enhance pain relief and reduce recurrence. Unlike pure NSAID therapy, the presence of sumatriptan provides targeted vasoconstriction, making the combination especially effective for moderate to severe attacks.

Nomigrin tablets should be stored at room temperature, below 25 °C, in the original packaging. Protect them from moisture, excessive heat and direct sunlight to maintain potency throughout the shelf life.

Nomigrin is taken orally with a full glass of water. It is usually taken at the onset of migraine symptoms, as directed by a healthcare professional. Swallow the tablet whole; do not crush or chew it.

Serious risks include coronary vasospasm, serotonin syndrome (especially when combined with other serotonergic drugs), severe allergic reactions, hypertension, gastrointestinal bleeding, and rare cerebrovascular events such as stroke. Patients should seek immediate medical attention if any of these occur.

Nomigrin is contraindicated in patients with known hypersensitivity to either component, uncontrolled cardiovascular disease, severe hepatic impairment, or those currently taking MAO inhibitors, other triptans, or ergot derivatives. A thorough medical review is essential before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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