Product image of Nitroplast (Glyceryl Trinitrate) supplied by GNH India

Nitroplast

Active Ingredient:
Glyceryl Trinitrate
Origin:
EU

Nitroplast (Glyceryl Trinitrate)

Glyceryl trinitrate, the active ingredient in Nitroplast, is a nitrate vasodilator presented as an unknown/transdermal patch for transdermal use. It is employed for the prophylaxis of angina pectoris and the management of chronic stable angina in adult patients.

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

Manufacturer / TM Owner

Lacer S.A.

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Indications & Clinical Uses

Nitroplast, a nitrate vasodilator, is used in the treatment of coronary artery disease‑related chest pain.

  • Prophylaxis of angina pectoris: reduces the frequency of anginal attacks during daily activities.
  • Management of chronic stable angina: improves exercise tolerance and decreases myocardial oxygen demand.
  • Ischemic heart disease: alleviates chest pain associated with reduced coronary blood flow.

How It Works

  • Glyceryl trinitrate is metabolized to nitric oxide, which activates guanylate cyclase in vascular smooth muscle. The resulting increase in cyclic GMP leads to relaxation of arterial and venous vessels, producing vasodilation, lowering preload and afterload, and consequently reducing myocardial oxygen consumption.

Side Effects

Nitroplast may cause a range of adverse reactions, most of which are related to its vasodilatory action.

Common Side Effects

  • Headache: throbbing pain often occurring shortly after patch application.
  • Flushing: warm sensation and redness of the skin.
  • Dizziness or light‑headedness: due to transient blood pressure reduction.
  • Skin irritation at the patch site: erythema or itching.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure requiring medical attention.
  • Syncope: fainting episodes caused by abrupt circulatory changes.
  • Life‑threatening allergic reaction: rash, swelling, or breathing difficulty.
  • Worsening angina or myocardial infarction: paradoxical increase in chest pain.
  • Methemoglobinemia: rare disorder impairing oxygen delivery.

Precautions & Warnings

When prescribing Nitroplast, clinicians should consider several safety measures.

  • Severe anemia: avoid use as it may exacerbate hypotension.
  • Concomitant phosphodiesterase‑5 inhibitors: risk of profound blood pressure fall; avoid combination.
  • Blood pressure monitoring: check regularly, especially after initiating therapy.
  • Patch site rotation: change location with each application to minimize skin irritation.
  • Store at room temperature: keep in original packaging, protect from moisture and light.

Avoid Interactions

Nitroplast can interact with other medicines, altering its safety profile.

Major Interactions (Avoid)

  • Sildenafil, tadalafil, or other PDE‑5 inhibitors: may cause severe hypotension.
  • Other nitrates (e.g., isosorbide dinitrate): additive vasodilatory effect leading to dangerous blood pressure drops.
  • Alcohol: potentiates hypotensive action.

Moderate Interactions (Monitor Closely)

  • Antihypertensives such as ACE inhibitors or beta‑blockers: may enhance blood pressure lowering.
  • Diuretics: increase risk of orthostatic hypotension.
  • Certain anti‑arrhythmic agents: may require dose adjustments.

Frequently Asked Questions

Nitroplast is a transdermal patch that delivers glyceryl trinitrate, a nitrate vasodilator, to prevent angina pectoris attacks and to manage chronic stable angina by improving blood flow to the heart muscle.

Glyceryl trinitrate releases nitric oxide, which activates guanylate cyclase in vascular smooth muscle. This raises cyclic GMP levels, causing relaxation of arteries and veins, lowering cardiac workload and oxygen demand, and thereby relieving angina.

The prescribed dose of Nitroplast is determined by the treating physician based on the individual’s clinical condition, severity of angina, and response to therapy. Patients should follow the specific instructions provided by their healthcare professional.

The safety of Nitroplast in pregnancy or while breastfeeding has not been definitively established. Healthcare providers should weigh potential benefits against possible risks before prescribing it to pregnant or nursing women.

To order Nitroplast, 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 necessary import documentation.

Nitroplast provides continuous delivery of glyceryl trinitrate via a patch, offering steady plasma levels compared with short‑acting oral nitrates. This can reduce dosing frequency and improve adherence, though it shares similar vasodilatory side effects with other nitrate preparations.

Nitroplast should be stored at room temperature, below 25 °C, in its original packaging. Keep the patches away from moisture, direct sunlight, and heat sources to maintain their integrity and efficacy.

The patch is applied to clean, dry, hair‑free skin on the upper torso or upper arm. The prescriber determines the duration of each application, typically ranging from 12 to 24 hours, after which a new patch is placed on a different site.

Serious risks include severe hypotension, syncope, life‑threatening allergic reactions, and worsening angina or myocardial infarction. Patients should seek immediate medical attention if they experience fainting, chest pain, or signs of an allergic response.

Nitroplast is contraindicated in patients with known hypersensitivity to glyceryl trinitrate or other nitrates, severe anemia, uncontrolled hypotension, and those concurrently using phosphodiesterase‑5 inhibitors due to the risk of dangerous blood pressure drops.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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