Product image of Lerkanidipin Zentiva (Lercanidipine Hydrochloride) supplied by GNH India

Lerkanidipin Zentiva

Active Ingredient:
Lercanidipine Hydrochloride
Origin:
EU

Lerkanidipin Zentiva (Lercanidipine Hydrochloride)

Lercanidipine, the active ingredient in Lerkanidipin Zentiva, is a calcium channel blocker presented as an oral tablet for oral use. It is employed to lower elevated blood pressure in adult patients with hypertension, helping to reduce cardiovascular risk.

GNH India supplies Lerkanidipin Zentiva as a licensed, GDP‑compliant international pharmaceutical supplier, providing quality‑assured medication to hospitals, pharmacies and clinics worldwide. Our distribution network adheres to global standards, facilitating reliable access across multiple regions.

Manufacturer / TM Owner

Zentiva, K.S.

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Indications & Clinical Uses

  • Lercanidipine is a calcium channel blocker used in the management of hypertension.
  • Hypertension: reduction of systolic and diastolic blood pressure, improving cardiovascular outcomes.

How It Works

  • Lercanidipine selectively inhibits L-type calcium channels in vascular smooth muscle, preventing calcium influx. This leads to relaxation of arterial smooth muscle, vasodilation, and a consequent decrease in peripheral vascular resistance, which lowers systemic blood pressure.

Side Effects

Lercanidipine may cause several adverse reactions that vary in frequency and severity.

Common Side Effects

  • Headache: mild to moderate pain often occurring shortly after dosing.
  • Flushing: transient warmth and redness of the skin, especially on the face.
  • Peripheral edema: swelling of the lower limbs due to fluid accumulation.
  • Dizziness: sensation of light‑headedness, particularly when standing quickly.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure that can cause fainting.
  • Angioedema: rapid swelling of the face, lips, tongue, or throat, potentially compromising airway.
  • Hepatotoxicity: rare liver injury manifested by elevated enzymes or jaundice.

Precautions & Warnings

  • When prescribing or dispensing Lercanidipine, several safety considerations should be observed.
  • Monitor blood pressure: adjust therapy based on regular measurements.
  • Avoid abrupt discontinuation: taper under medical supervision to prevent rebound hypertension.
  • Caution in hepatic impairment: dose may need adjustment due to metabolism reliance on the liver.
  • Use with caution in elderly patients: increased sensitivity to vasodilatory effects.
  • Store at ambient temperature below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Lercanidipine can interact with other medicines, influencing its efficacy or safety.

Major Interactions (Avoid)

  • Concomitant use with strong CYP3A4 inhibitors (e.g., ketoconazole): may increase plasma levels leading to excessive hypotension.
  • Co‑administration with other antihypertensives (e.g., ACE inhibitors, beta‑blockers): may cause additive blood‑pressure lowering.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampicin) may reduce drug exposure and effectiveness.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) may blunt the antihypertensive response.
  • Grapefruit juice may increase systemic exposure, requiring careful monitoring.

Frequently Asked Questions

Lerkanidipin Zentiva contains lercanidipine hydrochloride, a calcium channel blocker indicated for the treatment of hypertension. It helps lower elevated blood pressure by relaxing arterial smooth muscle, thereby reducing cardiovascular risk in adult patients.

Lercanidipine selectively blocks L‑type calcium channels in vascular smooth muscle. By inhibiting calcium entry, it causes vasodilation, decreases peripheral vascular resistance, and ultimately reduces systemic blood pressure.

The dosage of Lerkanidipin Zentiva is determined by the prescribing healthcare professional based on the patient’s clinical condition, response, and any comorbidities. The prescriber will set the appropriate strength and frequency.

Safety data for lercanidipine in pregnancy and lactation are limited, and the product is generally not recommended for use unless the potential benefit justifies the potential risk. Physicians should evaluate each case individually.

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.

Lercanidipine belongs to the dihydropyridine class of calcium channel blockers, offering potent vasodilatory effects with a relatively favorable side‑effect profile compared with some older agents. It is often considered when patients need effective blood‑pressure control with once‑daily dosing.

Lerkanidipin Zentiva tablets should be stored at ambient temperature below 25 °C, in the original packaging, and protected from moisture and direct sunlight to maintain product stability.

The medication is taken orally, usually once daily, with or without food, as directed by the prescribing clinician. Swallow the tablet whole with a glass of water; do not crush or chew unless specifically instructed.

Serious adverse events, though rare, include severe hypotension, angioedema, and hepatic injury. Patients should be advised to seek immediate medical attention if they experience sudden dizziness, swelling of the face or throat, or signs of liver dysfunction such as jaundice.

Lerkanidipin Zentiva is contraindicated in patients with known hypersensitivity to lercanidipine or any component of the formulation, and it should be used with caution in individuals with severe hepatic impairment or unstable angina. A healthcare professional should assess suitability before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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