Product image of Nifelat (Nifedipine) supplied by GNH India

Nifelat

Active Ingredient:
Nifedipine
Origin:
EU

Nifelat (Nifedipine)

Nifedipine, the active ingredient in Nifelat, is a calcium channel blocker presented as an oral tablet for systemic use. It is employed to manage high blood pressure, relieve chest pain from angina, and improve blood flow in Raynaud's phenomenon, primarily in adult patients.

GNH India supplies Nifelat as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with established quality‑assurance processes and regulatory approvals across multiple jurisdictions. Our distribution network ensures reliable delivery and compliance with local import requirements.

Manufacturer / TM Owner

Remedica Ltd

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Indications & Clinical Uses

Nifelat (nifedipine) acts on the cardiovascular system by relaxing vascular smooth muscle, making it useful for several related conditions.

  • Hypertension: reduces systemic vascular resistance, leading to lower arterial pressure and improved blood pressure control.
  • Angina pectoris: dilates coronary arteries and decreases cardiac workload, helping to prevent chest pain episodes.
  • Raynaud's phenomenon: improves peripheral blood flow by relaxing arterioles, reducing the frequency and severity of vasospastic attacks.

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, causing vasodilation of peripheral and coronary vessels. The resulting decrease in peripheral resistance lowers blood pressure, while coronary vasodilation improves myocardial oxygen supply. Its action is dose‑dependent and reversible, providing controlled hemodynamic effects without significant negative inotropy at therapeutic doses.

Side Effects

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

Common Side Effects

  • Flushing: warm sensation and redness of the skin.
  • Headache: often mild to moderate intensity.
  • Peripheral edema: swelling of ankles or feet.
  • 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 possible cardiac event.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Allergic reactions: rash, itching, or anaphylaxis.
  • Atrioventricular block: conduction disturbances.
  • Pulmonary edema: fluid accumulation in lungs.

Precautions & Warnings

When prescribing Nifelat, clinicians should consider several safety measures to minimize risks.

  • Blood pressure monitoring: check baseline and periodic readings.
  • Gradual dose titration: avoid abrupt dose changes to reduce hypotension risk.
  • Hepatic impairment: use caution and consider dose adjustment.
  • Concomitant antihypertensives: monitor for additive blood‑pressure‑lowering effects.
  • Pregnancy and lactation: evaluate risk‑benefit and consult obstetric guidance.
  • Store at ambient temperature: keep below 25 °C in original packaging, protect from moisture and light.

Avoid Interactions

Nifelat can interact with other medicines, altering its effectiveness or safety profile.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may cause dangerous hypotension.
  • Concurrent use with other potent vasodilators (e.g., nitroglycerin): risk of excessive blood pressure drop.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce nifedipine plasma levels.
  • Grapefruit juice: can increase drug concentration, enhancing side effects.
  • Beta‑blockers: may mask tachycardia, requiring heart rate monitoring.
  • Diuretics: additive effect on blood pressure, monitor electrolytes.
  • Antacids containing aluminum or magnesium: may affect absorption, separate dosing by at least 2 hours.

Frequently Asked Questions

Nifelat contains nifedipine, a calcium channel blocker indicated for the treatment of hypertension, angina pectoris, and Raynaud's phenomenon. By relaxing blood vessels, it helps lower high blood pressure, reduces chest pain caused by reduced coronary blood flow, and improves peripheral circulation in patients with vasospastic disorders.

Nifedipine blocks L‑type calcium channels in vascular smooth muscle and cardiac cells. This inhibition prevents calcium entry, reducing muscle contraction and causing vasodilation of peripheral and coronary arteries. The resulting drop in peripheral resistance lowers arterial pressure, while coronary dilation improves oxygen delivery to the heart.

The appropriate dose of Nifelat is determined by the prescribing healthcare professional based on the patient’s condition, response, and other clinical factors. Dosage regimens may differ for hypertension, angina, or Raynaud's phenomenon, and adjustments are made according to therapeutic goals and tolerability.

Safety of nifedipine in pregnancy and lactation has not been definitively established. Physicians should weigh potential benefits against possible risks and consider alternative therapies when appropriate. Women who are pregnant, planning pregnancy, or breastfeeding should discuss treatment options with their obstetric or primary care provider.

To request Nifelat, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, confirming trade or institutional credentials before providing pricing, availability, shipping details (including any cold‑chain requirements), and necessary import documentation.

Nifelat (nifedipine) belongs to the calcium channel blocker class, offering rapid vasodilation and effective blood‑pressure control. Compared with ACE inhibitors or beta‑blockers, it may produce more pronounced peripheral edema but is useful when patients cannot tolerate those classes. Choice of therapy depends on individual comorbidities, side‑effect profiles, and physician preference.

Store Nifelat at ambient temperature, preferably below 25 °C, in its original container to protect it from moisture and light. Keep the product out of reach of children and avoid storing it in bathrooms or other humid environments. Do not use if the packaging is damaged or the tablet appears discolored.

Nifelat is taken orally, usually with a glass of water. It may be taken with or without food, but consistent administration with respect to meals can help maintain stable drug levels. Patients should follow the prescribing clinician’s instructions regarding timing, dosage, and whether the tablet should be swallowed whole or split.

Serious adverse events, although rare, include severe hypotension, myocardial infarction, hepatic dysfunction, and life‑threatening allergic reactions such as anaphylaxis. Patients should seek immediate medical attention if they experience sudden weakness, chest pain, yellowing of the skin or eyes, or signs of a severe allergic response.

Nifelat is contraindicated in patients with known hypersensitivity to nifedipine or any other calcium channel blocker. It should also be avoided in individuals with severe aortic stenosis, uncontrolled heart failure, or cardiogenic shock, as the vasodilatory effect may worsen these conditions. Clinicians must assess each patient’s medical history before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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