Product image of Nimodrel Xl (Nifedipine) supplied by GNH India

Nimodrel Xl

Active Ingredient:
Nifedipine
Origin:
EU

Nimodrel Xl (Nifedipine)

Nifedipine, the active ingredient in Nimodrel Xl, is a calcium channel blocker (dihydropyridine) presented as an oral formulation for oral use. It lowers blood pressure and relieves chest pain in adults with hypertension or angina pectoris.

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

Manufacturer / TM Owner

Chiesi Limited

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Indications & Clinical Uses

Nifedipine acts on the vascular smooth muscle and coronary circulation to manage cardiovascular conditions.

  • Hypertension: reduces systemic vascular resistance and lowers arterial pressure.
  • Angina pectoris: decreases myocardial oxygen demand and alleviates chest pain episodes.
  • Raynaud's phenomenon: improves peripheral blood flow and reduces vasospastic attacks.

How It Works

  • Nifedipine selectively blocks L‑type calcium channels in vascular smooth muscle and cardiac myocytes. By inhibiting calcium influx, it causes arterial vasodilation, reduces peripheral resistance, and lowers cardiac after‑load, which together decrease blood pressure and myocardial oxygen consumption.

Side Effects

Nifedipine may cause a range of adverse reactions, most of which are dose‑related and reversible.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Flushing: warmth and redness of the face or neck.
  • Peripheral edema: swelling of ankles or lower legs.
  • Dizziness or light‑headedness.
  • Tachycardia: increased heart rate.
  • Nausea or abdominal discomfort.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure.
  • Myocardial infarction: rare but reported in high‑risk patients.
  • Hepatic dysfunction: elevated liver enzymes.
  • Allergic reactions: rash, pruritus, or anaphylaxis.
  • Cardiac arrhythmias: irregular heart rhythms.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for potential complications.

  • Blood pressure monitoring: check regularly to avoid excessive hypotension.
  • Hepatic impairment: use with caution and adjust dose if needed.
  • Concomitant antihypertensives: assess for additive blood‑pressure lowering effects.
  • Abrupt discontinuation: taper gradually to prevent rebound hypertension.
  • Pregnancy and lactation: evaluate risk‑benefit ratio; limited data available.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nifedipine can interact with several drug classes, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase nifedipine plasma levels and risk of toxicity.
  • Grapefruit juice: potentiates vasodilatory effect and can cause severe hypotension.
  • Concurrent use with other potent vasodilators: may lead to additive hypotensive episodes.

Moderate Interactions (Monitor Closely):\n- CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce therapeutic effect.

  • Diuretics: can enhance blood‑pressure lowering, requiring dose adjustments.
  • Beta‑blockers: may mask tachycardia, necessitating careful heart‑rate monitoring.
  • NSAIDs: may blunt antihypertensive response.
  • Anticoagulants: monitor for potential changes in bleeding risk.

Frequently Asked Questions

Nimodrel Xl contains nifedipine, a calcium channel blocker that is prescribed to lower high blood pressure and to relieve chest pain caused by angina pectoris. It may also be used in certain cases of Raynaud's phenomenon to improve peripheral blood flow.

Nifedipine blocks L‑type calcium channels on vascular smooth muscle and cardiac cells. This inhibition reduces calcium entry, leading to arterial dilation, lower peripheral resistance, and decreased cardiac workload, which together help control blood pressure and reduce myocardial oxygen demand.

The appropriate dose of Nimodrel Xl is determined by the prescribing clinician based on the patient’s condition, response, and other medical factors. Patients should follow the dosage instructions provided by their healthcare professional and not adjust the dose on their own.

Safety data for nifedipine in pregnancy and lactation are limited. The drug should only be used if the potential benefit justifies any possible risk to the fetus or infant. Pregnant or nursing women must discuss treatment options with their healthcare provider.

To place an order, submit an enquiry on the Nimodrel Xl 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.

Nimodrel Xl (nifedipine) belongs to the dihydropyridine class of calcium channel blockers, which primarily cause arterial vasodilation. Compared with beta‑blockers or ACE inhibitors, it has a more pronounced effect on peripheral vessels and may cause flushing or edema, but it is effective for patients who need rapid blood‑pressure reduction.

Nimodrel Xl should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture and direct sunlight to maintain stability and potency throughout its shelf life.

Nimodrel Xl is taken orally, usually with a glass of water. The tablet should be swallowed whole and not chewed or crushed unless otherwise directed by a healthcare professional.

Serious risks include severe hypotension, myocardial infarction, hepatic dysfunction, allergic reactions such as rash or anaphylaxis, and cardiac arrhythmias. Patients should seek immediate medical attention if they experience symptoms like fainting, chest pain, or unusual heart rhythms.

Nimodrel Xl is contraindicated in patients with known hypersensitivity to nifedipine or any other dihydropyridine calcium channel blocker. It should also be avoided in individuals with severe aortic stenosis, uncontrolled heart failure, or those taking certain strong CYP3A4 inhibitors without medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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