Product image of Lercanidipine Eg (Lercanidipine Hydrochloride) supplied by GNH India

Lercanidipine Eg

Active Ingredient:
Lercanidipine Hydrochloride
Origin:
EU

Lercanidipine Eg (Lercanidipine Hydrochloride)

Lercanidipine Hydrochloride, the active ingredient in Lercanidipine Eg, is a calcium channel blocker presented as a tablet for oral use. It treats hypertension in adult patients by lowering systemic vascular resistance.

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

Manufacturer / TM Owner

Eurogenerics N.V./S.A.

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Indications & Clinical Uses

Lercanidipine is a dihydropyridine calcium‑channel blocker used to manage high‑blood‑pressure disorders.

  • Essential hypertension: reduces both systolic and diastolic blood pressure.
  • Isolated systolic hypertension: improves arterial compliance and lowers systolic pressure.
  • Secondary hypertension (e.g., renovascular): assists in blood‑pressure control when combined with other antihypertensives.

How It Works

  • Lercanidipine selectively blocks L‑type calcium channels on vascular smooth‑muscle cells, inhibiting calcium influx. This causes dose‑dependent vasodilation of peripheral arteries, decreasing systemic vascular resistance and consequently lowering arterial blood pressure without significant negative inotropic effects.

Side Effects

Adverse reactions may occur with any antihypertensive therapy.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Flushing: transient warmth and redness of the skin.
  • Peripheral edema: swelling of ankles or lower legs.
  • Dizziness: especially on standing.
  • Tachycardia: increased heart rate.
  • Nausea: occasional gastrointestinal upset.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure requiring medical attention.
  • Myocardial infarction: rare occurrence of heart attack.
  • Hepatic dysfunction: abnormal liver enzymes or hepatitis.
  • Allergic reactions: angioedema, rash, or anaphylaxis.
  • Arrhythmias: abnormal heart rhythms.
  • Heart block: conduction disturbances.

Precautions & Warnings

Before prescribing Lercanidipine, clinicians should consider several safety factors.

  • Blood pressure monitoring: check baseline and periodic readings.
  • Cardiovascular disease: use cautiously in severe aortic stenosis or heart failure.
  • Liver impairment: dose adjustment may be needed.
  • Elderly patients: initiate at the lowest effective dose.
  • Drug interactions: review concomitant medications for CYP3A4 substrates.
  • Store at ambient temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Lercanidipine may interact with other medicines that affect its metabolism or hemodynamic effects.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole): can raise plasma concentrations.
  • Grapefruit juice: may increase drug exposure.
  • Co‑administration with other calcium‑channel blockers: risk of additive hypotension.

Moderate Interactions (Monitor Closely):\n- Diuretics: may enhance antihypertensive effect, requiring BP monitoring.

  • Beta‑blockers: combined use can cause excessive bradycardia.
  • ACE inhibitors or ARBs: monitor renal function and potassium levels.

Frequently Asked Questions

Lercanidipine Eg contains the active ingredient lercanidipine hydrochloride, which is prescribed to lower high blood pressure in adults. It belongs to the calcium‑channel blocker class and works by relaxing the smooth muscle of blood vessels, thereby reducing systemic vascular resistance.

Lercanidipine selectively blocks L‑type calcium channels on vascular smooth‑muscle cells. By preventing calcium entry, it causes dose‑dependent vasodilation of peripheral arteries, which decreases peripheral resistance and results in a reduction of arterial blood pressure.

The appropriate dose of Lercanidipine Eg is determined by the prescribing clinician based on the patient’s blood‑pressure profile, age, renal and hepatic function, and concomitant therapies. The prescriber will select the starting dose and any subsequent adjustments.

The safety of lercanidipine in pregnancy and lactation has not been established. It is classified as pregnancy category unknown, and clinicians usually avoid its use unless the potential benefit justifies the potential risk to the fetus or infant.

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 required import documentation.

Lercanidipine, as a dihydropyridine calcium‑channel blocker, primarily induces arterial vasodilation, whereas beta‑blockers reduce cardiac output and ACE inhibitors block the renin‑angiotensin system. Lercanidipine often provides a smoother blood‑pressure reduction with a lower incidence of reflex tachycardia compared with some other calcium‑channel blockers.

Lercanidipine Eg tablets should be stored at ambient temperature, below 25 °C, in the original container to protect them from moisture and light. Do not store in a humid environment or expose the product to excessive heat.

Lercanidipine Eg is taken orally, usually once daily, with or without food, as directed by the prescriber. Swallow the tablet whole with a glass of water; do not crush or chew it unless specifically instructed.

Serious adverse events, although rare, include severe hypotension, myocardial infarction, hepatic dysfunction, allergic reactions such as angioedema, and cardiac conduction disturbances like heart block. Patients should seek immediate medical attention if they experience symptoms such as faintness, chest pain, jaundice, rash, or irregular heartbeat.

Lercanidipine is contraindicated in patients with known hypersensitivity to lercanidipine or any component of the formulation. Caution is advised in individuals with severe aortic stenosis, unstable angina, or those taking strong CYP3A4 inhibitors, as these conditions may increase the risk of adverse effects.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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