Product image of Nifedipine Retard Eg (Nifedipine) supplied by GNH India

Nifedipine Retard Eg

Active Ingredient:
Nifedipine
Origin:
EU

Nifedipine Retard Eg (Nifedipine)

Nifedipine, the active ingredient in Nifedipine Retard Eg, is a calcium channel blocker presented as an extended‑release tablet for oral use. It is employed to lower high blood pressure and to relieve chest pain caused by chronic stable angina in adult patients.

GNH India supplies Nifedipine Retard Eg as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with sourcing from the European Union market. The company adheres to stringent quality standards and provides regulatory documentation to facilitate import and distribution.

Manufacturer / TM Owner

Eurogenerics N.V./S.A.

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Indications & Clinical Uses

  • Nifedipine is used in cardiovascular therapy to manage conditions related to elevated vascular resistance and myocardial oxygen demand.
  • Hypertension: Reduces systemic blood pressure by dilating peripheral arteries.
  • Chronic stable angina: Improves exercise tolerance and decreases frequency of chest pain episodes.
  • Coronary artery disease symptom control: Alleviates ischemic symptoms by decreasing cardiac workload.

How It Works

  • Nifedipine selectively blocks L‑type calcium channels in vascular smooth muscle and cardiac myocytes. By inhibiting calcium influx, it prevents contraction of arterial smooth muscle, producing arterial vasodilation and lowering peripheral resistance. In the heart, reduced calcium entry decreases contractility and myocardial oxygen consumption, contributing to its anti‑anginal effect. The extended‑release formulation provides a gradual onset and sustained plasma concentrations, allowing once‑daily dosing.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate headache often occurring early in therapy.
  • Flushing: transient warmth and redness of the face or neck.
  • Peripheral edema: swelling of ankles or lower legs due to fluid accumulation.
  • Dizziness or light‑headedness: especially upon standing.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure leading to fainting.
  • Cardiac arrhythmias: irregular heart rhythms, particularly in patients with pre‑existing conduction disorders.
  • Hepatic dysfunction: elevated liver enzymes or jaundice.

Precautions & Warnings

When prescribing Nifedipine, clinicians should consider several precautionary measures to ensure safe use.

  • Assess cardiovascular status: evaluate blood pressure and heart rate before initiating therapy.
  • Review concomitant medications: avoid drugs that may potentiate hypotensive effects.
  • Monitor in hepatic impairment: dose adjustment may be required in patients with liver dysfunction.
  • Caution in elderly patients: start with lower doses and observe for orthostatic symptoms.
  • Store at ambient temperature: keep tablets below 25 °C in the original container, protected from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): can markedly increase nifedipine plasma levels, raising risk of severe hypotension.
  • Grapefruit juice: potent CYP3A4 inhibition may lead to excessive drug accumulation and adverse events.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: combined use may cause additive bradycardia or heart block; monitor heart rate.
  • Diuretics: concurrent therapy may enhance hypotensive effect; adjust dose as needed.
  • Other calcium channel blockers: additive vasodilatory effects may increase risk of edema; observe patient response.

Frequently Asked Questions

Nifedipine Retard Eg is prescribed to lower high blood pressure (hypertension) and to relieve chest pain associated with chronic stable angina. By reducing vascular resistance and myocardial oxygen demand, it helps prevent cardiovascular complications in adult patients.

Nifedipine blocks L‑type calcium channels in arterial smooth muscle and cardiac cells. This inhibition prevents calcium‑driven contraction, causing vasodilation of peripheral arteries and reducing the workload of the heart, which lowers blood pressure and eases angina symptoms.

The exact dose is determined by the prescribing clinician based on the individual’s medical condition, response to therapy, and any co‑existing health issues. Physicians typically start with a low dose and may adjust it to achieve the desired blood‑pressure or anti‑anginal effect.

Safety data for Nifedipine during pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

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.

Nifedipine belongs to the calcium‑channel blocker class, offering potent arterial vasodilation. Compared with beta‑blockers, it primarily reduces peripheral resistance rather than heart rate. Compared with ACE inhibitors, it does not affect the renin‑angiotensin system, making it a useful alternative or add‑on when those agents are contraindicated or insufficient.

Store the tablets at ambient temperature, preferably below 25 °C, in the original blister pack or container. Protect them from excess moisture and direct sunlight. Do not refrigerate or freeze the product, as temperature extremes can affect tablet integrity.

The medication is taken orally, usually once daily, with a full glass of water. Tablets should be swallowed whole and not chewed, crushed, or split, to maintain the extended‑release profile and ensure consistent drug absorption.

The most critical adverse events include severe hypotension, which can cause fainting or shock, cardiac arrhythmias especially in patients with pre‑existing conduction disorders, and rare cases of hepatic dysfunction indicated by elevated liver enzymes or jaundice. Prompt medical attention is required if these symptoms appear.

Patients with known hypersensitivity to nifedipine or any component of the formulation should avoid it. It is also contraindicated in individuals with severe aortic stenosis, cardiogenic shock, or uncontrolled heart failure, as the vasodilatory effect may worsen these conditions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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