Product image of Migranal (Dihydroergotamine Mesilate) supplied by GNH India

Migranal

Active Ingredient:
Dihydroergotamine Mesilate
Origin:
EU

Migranal (Dihydroergotamine Mesilate)

Dihydroergotamine mesilate, the active ingredient in Migranal, is an ergot alkaloid presented as a 1 mg per spray nasal spray for nasal use. Approved in the European Union, it is indicated for the acute treatment of migraine attacks in adults, delivering rapid relief of headache and associated symptoms.

GNH India supplies Migranal as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring reliable supply chain management across global markets.

Manufacturer / TM Owner

Amdipharm Uk Limited

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Indications & Clinical Uses

Dihydroergotamine mesilate is used to abort acute migraine attacks by modulating serotonergic and vascular pathways involved in migraine pathophysiology.

  • Acute migraine: provides rapid relief of headache pain and associated nausea or photophobia.
  • Migraine attacks: aborts ongoing migraine episodes when administered at onset.
  • Status migrainosus: may be employed for severe, prolonged migraine attacks unresponsive to other therapies.

How It Works

  • Dihydroergotamine mesilate acts as a partial agonist at serotonin 5‑HT1 receptors while antagonizing alpha‑adrenergic and dopaminergic receptors. This dual activity produces vasoconstriction of intracranial vessels and reduces neurogenic inflammation, helping to terminate migraine attacks.

Side Effects

Dihydroergotamine mesilate may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Nasal irritation or burning sensation.
  • Nausea or vomiting.
  • Dizziness or light‑headedness.
  • Dry mouth.
  • Fatigue or drowsiness.

Serious or Rare Side Effects

  • Severe vasospasm leading to hypertension or myocardial ischemia.
  • Peripheral ischemia or gangrene.
  • Anaphylaxis or severe allergic reaction.
  • Serotonin syndrome, especially when combined with serotonergic agents.

Precautions & Warnings

When prescribing Migranal, clinicians should consider several precautionary measures to minimize risk.

  • Cardiovascular disease: avoid use in patients with coronary artery disease or uncontrolled hypertension.
  • Peripheral vascular disease: contraindicated in individuals with severe peripheral arterial insufficiency.
  • Pregnancy and lactation: use only if the potential benefit justifies the potential risk.
  • Drug interactions: monitor closely when combined with serotonergic or ergot‑containing medications.
  • Hepatic impairment: dose adjustment may be required in severe liver disease.
  • Store below 25°C: keep in the original pack, protect from moisture and light.

Avoid Interactions

Dihydroergotamine mesilate can interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): risk of severe hypertension and serotonin syndrome.
  • Other ergot derivatives: additive vasoconstrictive effects.
  • Serotonergic agents (SSRIs, SNRIs, triptans): increased risk of serotonin syndrome.

Moderate Interactions (Monitor Closely):\n- Strong CYP3A4 inhibitors (e.g., ketoconazole): may raise dihydroergotamine levels.

  • CYP3A4 inducers (e.g., rifampin): may reduce therapeutic effect.
  • Antihypertensive drugs: potential additive blood pressure changes.

Frequently Asked Questions

Migranal is a prescription nasal spray containing dihydroergotamine mesilate, indicated for the acute treatment of migraine attacks in adults, including status migrainosus. It helps relieve headache pain and associated symptoms when administered at the onset of an attack.

Dihydroergotamine mesilate acts as a partial agonist at serotonin 5‑HT1 receptors and blocks alpha‑adrenergic and dopaminergic receptors. This results in constriction of intracranial blood vessels and suppression of neurogenic inflammation, which together abort migraine episodes.

The prescribed dose of Migranal is determined by the treating physician. Each spray delivers 1 mg of dihydroergotamine mesilate, and the number of sprays per migraine attack is individualized based on clinical response and tolerability.

Safety of dihydroergotamine mesilate during pregnancy or lactation has not been established. It should be used only if the potential benefit justifies the potential risk to the fetus or infant, and the prescriber must evaluate each case carefully.

To order Migranal, 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.

Compared with triptans, dihydroergotamine offers a non‑triptan abortive option that can be effective in patients who do not respond to or cannot take triptans. Its nasal spray formulation provides rapid absorption, but it carries a distinct vasoconstrictive side‑effect profile that requires careful patient selection.

Store Migranal nasal spray below 25 °C in its original packaging. Protect the device from moisture, heat and direct sunlight. Do not freeze the product, and keep the spray cap tightly closed when not in use.

Migranal is given intranasally. The patient tilts the head slightly forward, inserts the nozzle into one nostril, and actuates the pump to deliver a single spray (1 mg). The dose may be repeated as directed by the prescriber, typically with a minimum interval between sprays.

Serious adverse events include severe vasoconstriction leading to hypertension, myocardial or peripheral ischemia, rare cases of serotonin syndrome, and anaphylaxis. Patients should seek immediate medical attention if they experience chest pain, severe headache, visual changes, or signs of an allergic reaction.

Migranal is contraindicated in individuals with known hypersensitivity to ergot alkaloids, uncontrolled hypertension, coronary artery disease, peripheral vascular disease, severe hepatic impairment, or in patients currently taking monoamine oxidase inhibitors. It should also be avoided in pregnancy unless clearly needed.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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