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 ingredient in Nomigrin, is a combined NSAID and selective 5‑HT1B/1D receptor agonist presented as an oral tablet formulation for oral administration. The combination provides both anti‑inflammatory analgesia and targeted migraine relief, and it is used 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, ensuring quality‑controlled manufacturing and regulatory compliance for global distribution to meet local market requirements.

Manufacturer / TM Owner

Orion Corporation

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Indications & Clinical Uses

Nomigrin belongs to the NSAID and triptan drug families and is used to manage migraine episodes.

  • Acute migraine attacks: rapid relief of headache, nausea, photophobia and phonophobia.
  • Migraine with aura: alleviates the headache phase that follows visual or sensory aura symptoms.
  • Migraine without aura: reduces pain intensity and associated symptoms when taken early in the attack.

How It Works

  • Naproxen sodium inhibits cyclooxygenase enzymes, decreasing prostaglandin synthesis and providing anti‑inflammatory analgesia. Sumatriptan succinate selectively activates 5‑HT1B/1D receptors on cranial blood vessels and trigeminal nerve endings, causing vasoconstriction and inhibition of neuropeptide release, which together abort migraine pain pathways.

Side Effects

Common Side Effects

  • Nausea or upset stomach
  • Dizziness or light‑headedness
  • Tingling or numbness in fingers or toes
  • Chest tightness or pressure
  • Flushing or warmth sensation
  • Dry mouth

Serious or Rare Side Effects

  • Coronary artery spasm or myocardial ischemia
  • Severe allergic reaction (anaphylaxis, angioedema)
  • Serotonin syndrome when combined with other serotonergic agents
  • Gastrointestinal bleeding or ulcer perforation
  • Hepatic dysfunction or elevated liver enzymes
  • Stroke or transient ischemic attack

Precautions & Warnings

Before prescribing Nomigrin, clinicians should consider the following precautions:

  • Cardiovascular assessment: evaluate for coronary artery disease or uncontrolled hypertension.
  • Serotonergic risk: avoid in patients taking other triptans, SSRIs, SNRIs, or MAO inhibitors.
  • Gastro‑intestinal safety: use caution in patients with a history of ulcers or bleeding.
  • Renal or hepatic impairment: dose adjustment may be required.
  • Hypersensitivity: discontinue if signs of allergic reaction appear.
  • Store at ambient temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Nomigrin may interact with several drug classes.

Major Interactions (Avoid)

  • SSRIs, SNRIs, or MAO inhibitors: increased risk of serotonin syndrome.
  • Other triptans or ergot derivatives: additive vasoconstrictive effects.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole): may raise sumatriptan levels.

Moderate Interactions (Monitor Closely)

  • Additional NSAIDs or aspirin: heightened gastrointestinal bleeding risk.
  • Antihypertensive agents (beta‑blockers, calcium channel blockers): may blunt blood pressure control.

Frequently Asked Questions

Nomigrin is a prescription oral tablet that combines naproxen sodium and sumatriptan succinate to provide rapid relief of acute migraine attacks in adults, addressing both headache pain and associated symptoms such as nausea and sensitivity to light.

Naproxen sodium reduces inflammation by inhibiting cyclooxygenase enzymes, lowering prostaglandin production. Sumatriptan succinate activates 5‑HT1B/1D receptors, causing cranial blood‑vessel constriction and blocking neuropeptide release, together aborting migraine pain pathways.

The dose of Nomigrin is determined by the prescribing clinician based on the patient’s medical history, severity of migraine, and other medications. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety of Nomigrin in pregnancy or while breastfeeding has not been fully established. Healthcare providers should weigh potential benefits against risks and consider alternative therapies if there are concerns about fetal or infant exposure.

To order 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 necessary import documentation.

Nomigrin combines an NSAID with a triptan, offering both anti‑inflammatory pain relief and targeted vasoconstriction. This dual mechanism can be more effective for some patients than using a single‑agent triptan or NSAID alone, but individual response varies and should be evaluated by a clinician.

Nomigrin tablets should be stored at ambient temperature, below 25 °C, in the original container to protect them from moisture and light. Keep the product out of reach of children and do not use after the expiry date.

Nomigrin is taken orally with a full glass of water, preferably at the first sign of a migraine attack. It should be swallowed whole and not chewed or crushed, unless otherwise directed by a healthcare professional.

Serious risks include coronary artery spasm, myocardial ischemia, serotonin syndrome when combined with other serotonergic drugs, severe allergic reactions, gastrointestinal bleeding, and rare events such as stroke. Patients should seek immediate medical attention if they experience chest pain, severe allergic signs, or neurological changes.

Nomigrin should be avoided in patients with known hypersensitivity to naproxen, sumatriptan, or any component of the formulation, those with uncontrolled hypertension, recent myocardial infarction, severe coronary artery disease, or who are currently taking MAO inhibitors, other triptans, or strong serotonergic agents.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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