Product image of Nicorandil Eg (Nicorandil) supplied by GNH India

Nicorandil Eg

Active Ingredient:
Nicorandil
Origin:
EU

Nicorandil Eg (Nicorandil)

Nicorandil, the active ingredient in Nicorandil Eg, is a potassium channel activator presented as an oral tablet for oral use. It is used to treat chronic stable angina in adult patients.

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

Manufacturer / TM Owner

Double-E Pharma Ltd

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Indications & Clinical Uses

Nicorandil is indicated for conditions involving myocardial oxygen demand and supply imbalance, primarily chronic stable angina.

  • Chronic stable angina: reduces frequency of angina attacks and improves exercise tolerance.
  • Variant (Prinzmetal) angina: helps prevent coronary artery spasm.
  • Post‑myocardial infarction angina: may aid in symptom control when other therapies are insufficient.

How It Works

  • Nicorandil acts as a nitrate‑like vasodilator while simultaneously opening ATP‑sensitive potassium channels in vascular smooth muscle. The combined effect leads to coronary and peripheral vasodilation, lowering both preload and afterload, which improves myocardial oxygen balance and relieves anginal symptoms.

Side Effects

Nicorandil may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Headache: mild to moderate, often transient.
  • Flushing: warmth and redness of the skin.
  • Dizziness or light‑headedness, especially on standing.
  • Nausea or abdominal discomfort.
  • Palpitations: sensation of rapid or irregular heartbeat.
  • Hypotension: mild drop in blood pressure.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure requiring medical attention.
  • Exacerbation of angina or myocardial infarction.
  • Ulceration or severe gastrointestinal irritation.
  • Allergic reactions such as rash or Stevens‑Johnson syndrome.
  • Syncope: sudden loss of consciousness.
  • Cardiogenic shock in extreme cases.

Precautions & Warnings

Before initiating Nicorandil therapy, several safety considerations should be observed.

  • Blood pressure monitoring: check baseline and periodic readings.
  • Concomitant nitrates: avoid combined use to prevent excessive vasodilation.
  • Hepatic impairment: use with caution in patients with liver dysfunction.
  • Severe hypotension: discontinue if symptomatic low blood pressure occurs.
  • Pregnancy and lactation: assess risk‑benefit; generally avoid unless clearly needed.
  • Store at below 25°C: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nicorandil can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Other nitrate preparations: risk of profound hypotension.
  • Phosphodiesterase‑5 inhibitors (e.g., sildenafil): may cause severe blood pressure fall.
  • Potent vasodilators (e.g., hydralazine): additive hypotensive effect.

Moderate Interactions (Monitor Closely)

  • Antihypertensive agents (ACE inhibitors, ARBs, beta‑blockers): may enhance blood pressure lowering.
  • Diuretics: monitor electrolytes and volume status.
  • Calcium channel blockers: watch for additive vasodilatory response.
  • Oral hypoglycemics: possible alteration of glucose control.
  • Antiplatelet or anticoagulant drugs: monitor for bleeding tendency.

Frequently Asked Questions

Nicorandil Eg is prescribed to manage chronic stable angina, a condition where the heart muscle receives insufficient oxygen during physical activity. By dilating coronary vessels and reducing cardiac workload, it helps relieve chest pain and improve exercise tolerance in adult patients.

Nicorandil combines nitrate‑like vasodilation with activation of ATP‑sensitive potassium channels in vascular smooth muscle. This dual action expands coronary and peripheral vessels, lowers both preload and afterload, and enhances myocardial oxygen supply while decreasing demand, thereby alleviating anginal symptoms.

The specific dose and dosing schedule of Nicorandil Eg are determined by the prescribing clinician based on the individual’s clinical condition, response, and tolerability. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Nicorandil is generally avoided during pregnancy and lactation unless the potential benefit justifies the risk. Healthcare providers should evaluate the maternal and fetal considerations carefully, and breastfeeding mothers should discuss alternatives with their physician.

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.

Nicorandil’s unique mechanism—combining nitrate‑like effects with potassium‑channel activation—differs from pure nitrates or beta‑blockers. This dual action can provide additional symptom relief for patients who remain symptomatic on standard therapy, though individual response varies and should be assessed by a physician.

Nicorandil Eg should be stored at temperatures below 25 °C in its original packaging. Protect the tablets from moisture, excessive heat and direct sunlight to maintain potency throughout its shelf life.

Nicorandil Eg is taken orally, usually with a glass of water. It may be taken with or without food, but patients should follow the prescriber’s guidance regarding timing relative to meals to minimize gastrointestinal discomfort.

The most serious risks include severe hypotension, worsening angina or myocardial infarction, and rare but serious skin reactions such as Stevens‑Johnson syndrome. Patients should seek immediate medical attention if they experience fainting, chest pain worsening, or severe skin eruptions.

Nicorandil is contraindicated in patients with known hypersensitivity to the drug, those taking other nitrate preparations, and individuals with severe hypotension or cardiogenic shock. Clinicians should also exercise caution in patients with significant hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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