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Migxen 85/500mg Tablets – Targeted Combination Acute Migraine Relief

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Relieve acute migraine attacks fast with Migxen 85/500mg Tablets. Fixed-dose Sumatriptan & Naproxen Sodium combo targeting pain, nausea, and light sensitivity.

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Description

Product Overview

Migxen 85/500mg Tablets are an advanced fixed-dose combination antimigraine therapy combining Sumatriptan Succinate (85mg) and Naproxen Sodium (500mg). Engineered specifically for the acute treatment of migraine attacks with or without aura in adults, Migxen addresses both the neurovascular cause and the inflammatory cascade of migraines. By combining a targeted 5-HT1B/1D receptor agonist (triptan) with a fast-acting nonsteroidal anti-inflammatory drug (NSAID), Migxen provides superior, longer-lasting relief from throbbing headache pain, photophobia (light sensitivity), phonophobia (sound sensitivity), and associated nausea compared to single-agent therapies.

Key Benefits

  • Dual-Mechanism Synergism: Delivers enhanced, long-lasting pain relief by targeting both neurogenic inflammation and cranial vasodilation simultaneously.

  • Reduces Migraine Recurrence: Combining Naproxen Sodium with Sumatriptan significantly lowers the rate of 24-hour migraine recurrence compared to triptan monotherapy.

  • Comprehensive Symptom Control: Effectively alleviates severe head pain, nausea, vomiting, photophobia, and phonophobia.

  • Rapid Onset of Action: Fast-dissolving formulation provides measurable pain relief within 30 to 60 minutes of ingestion.

  • Single-Tablet Convenience: Eliminates the need to take separate triptan and NSAID doses during an acute migraine attack.

How It Works

Migxen 85/500mg Tablets function via two distinct, complementary pathways:

  1. Sumatriptan (85mg): Selective serotonin receptor agonist. It binds to receptors on intracranial blood vessels and sensory nerve endings of the trigeminal system. This induces cranial vasoconstriction, suppresses trigeminal nerve activation, and inhibits the release of vasoactive pro-inflammatory neuropeptides (such as CGRP).

  2. Naproxen Sodium (500mg): Non-selective cyclooxygenase (COX-1 and COX-2) inhibitor. It inhibits the enzymatic synthesis of prostaglandins, preventing neurogenic inflammatory sensitization in central and peripheral pain pathways and halting sustained pain transmission.

Key Active Ingredients

  • Sumatriptan Succinate (equivalent to 85mg Sumatriptan): Vascular serotonin agonist that constricts swollen cranial vessels and inhibits neurogenic inflammatory peptide release.

  • Naproxen Sodium (500mg): Long-acting NSAID that inhibits prostaglandin synthesis to eliminate neurogenic tissue inflammation and prolonged headache pain.

Directions for Use

  1. Administration: Swallow 1 film-coated tablet whole with a full glass of water at the very first sign of a migraine attack. Do not crush, split, or chew the tablet.

  2. Dosing:

    • Adults (18 years and older): 1 tablet per acute migraine attack.

    • Second Dose: If the migraine returns or response is incomplete, a second dose may be taken at least 2 hours apart.

    • Maximum Dose: Do not exceed 2 tablets in any 24-hour period.

  3. Important Note: Not intended for prophylactic (preventative) treatment of migraines or for the management of hemiplegic or basilar migraines.

Precautions

  • Prescription-Only Medication: Take strictly as prescribed by a healthcare provider.

  • Cardiovascular & Cerebrovascular Warning: Contraindicated in patients with ischemic heart disease (e.g., angina, prior myocardial infarction), uncontrolled hypertension, coronary artery vasospasm (Prinzmetal’s angina), peripheral vascular disease, or history of stroke/TIA.

  • Gastrointestinal Risk: Contains Naproxen Sodium; use with caution in patients with a history of peptic ulcer disease or GI bleeding.

  • Serotonin Syndrome Risk: Exercise caution when co-administered with SSRIs, SNRIs, or other serotonergic medications. Contraindicated within 14 days of MAO inhibitor therapy.

  • Renal & Hepatic Impairment: Avoid use in severe hepatic impairment or severe renal insufficiency ().

  • Consult a physician before use during pregnancy or lactation (specifically avoid during late pregnancy due to early closure of the ductus arteriosus).

  • Keep out of reach of children.

Storage Instructions

Store in a cool, dry place below 30°C, protected from direct light, heat, and moisture. Keep tablets sealed in their original blister package until time of administration.

Manufacturer Information

Formulated and manufactured in strict compliance with international pharmaceutical quality standards, dedicated to providing advanced neurology and pain management therapies that restore quality of life and deliver fast, sustained relief.

Brand

PHARMASOL (PVT) LTD

Introducing PHARMASOL – your trusted partner in delivering excellence in pharmaceutical care. At PHARMASOL, we specialize in crafting premium syrups, injections, and tablets, redefining healthcare with innovation and precision. Our philosophy is rooted in enhancing lives, ensuring that each product reflects quality, safety, and reliability. We are committed to delivering high-quality products through our extensive Pharma Services Distribution, ensuring broad access to safe and dependable solutions across diverse markets.
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