Product image of Lercanidipin Actavis (Lercanidipine Hydrochloride) supplied by GNH India

Lercanidipin Actavis

Active Ingredient:
Lercanidipine Hydrochloride
Origin:
EU

Lercanidipin Actavis (Lercanidipine Hydrochloride)

Lercanidipine, the active ingredient in Lercanidipin Actavis, is a calcium channel blocker presented as an oral tablet for systemic use. It lowers elevated blood pressure and is indicated for the management of hypertension in adult patients, and is commonly prescribed as part of a comprehensive blood pressure management plan.

GNH India supplies Lercanidipin Actavis as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable global distribution for this antihypertensive medication.

Manufacturer / TM Owner

Actavis Group Ptc Ehf.

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Indications & Clinical Uses

  • Lercanidipine is used to treat conditions related to elevated vascular resistance and high blood pressure.
  • Hypertension: lowers systolic and diastolic blood pressure in adults with primary hypertension.
  • Essential hypertension: helps achieve guideline‑recommended blood pressure targets, either as monotherapy or in combination.
  • Isolated systolic hypertension: provides effective blood pressure reduction in elderly patients with isolated systolic hypertension.

How It Works

  • Lercanidipine selectively blocks L‑type calcium channels in vascular smooth muscle, inhibiting calcium influx that is necessary for muscle contraction. This vasodilatory effect reduces peripheral vascular resistance, leading to a decrease in arterial blood pressure without significant effect on cardiac conduction or contractility. The inhibition is dose‑dependent and preferentially affects arterial over venous vessels, resulting in sustained blood pressure lowering with minimal reflex tachycardia.

Side Effects

Lercanidipine may be associated with several adverse reactions, which are categorized by frequency and clinical significance.

Common Side Effects

  • Headache: mild to moderate headache occurring shortly after dose initiation.
  • Flushing: transient facial or upper body flushing.
  • Peripheral edema: swelling of ankles or lower limbs.
  • Dizziness: light‑headed sensation, especially when standing quickly.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure causing fainting.
  • Angioedema: swelling of face, lips, tongue or throat.
  • Myocardial infarction: rare occurrence of heart attack.

Precautions & Warnings

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

  • Assess cardiovascular status: evaluate for existing low blood pressure or heart failure before initiating therapy.
  • Monitor blood pressure: check regularly after starting treatment and after dose adjustments.
  • Caution in hepatic impairment: dose may need adjustment in patients with liver dysfunction.
  • Avoid abrupt discontinuation: taper gradually to prevent rebound hypertension.
  • Drug interactions: review concomitant medications that affect cytochrome P450 3A4.
  • Store at ambient temperature: keep below 25°C in the original container, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors: concurrent use with ketoconazole, itraconazole or clarithromycin can markedly increase plasma levels.
  • Grapefruit juice: may raise drug concentration and risk of hypotension.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers: rifampicin or carbamazepine may reduce effectiveness.
  • Other antihypertensives: additive blood pressure lowering when combined with beta‑blockers or ACE inhibitors.
  • Diuretics: may enhance orthostatic hypotension.

Frequently Asked Questions

Lercanidipin Actavis contains lercanidipine, a calcium channel blocker indicated for the treatment of hypertension. It helps lower elevated systolic and diastolic blood pressure in adult patients, contributing to cardiovascular risk reduction when used as part of a comprehensive antihypertensive regimen.

Lercanidipine selectively inhibits L‑type calcium channels in vascular smooth‑muscle cells, reducing calcium entry that drives muscle contraction. This causes arterial vasodilation, decreases peripheral resistance, and ultimately lowers systemic blood pressure without markedly affecting heart rate or cardiac output.

The appropriate dose of Lercanidipin Actavis is determined by the prescribing clinician based on the patient’s blood pressure, response to therapy, and any comorbid conditions. Dosage adjustments are made according to clinical judgment and current hypertension guidelines.

Safety data for lercanidipine during pregnancy and lactation are limited, and the product is generally not recommended for use in pregnant or nursing women unless the potential benefit outweighs the risk. Clinicians should evaluate alternatives and discuss potential risks with the patient.

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 calcium‑channel blocker class and offers potent arterial vasodilation with a relatively low incidence of reflex tachycardia. Compared with agents such as amlodipine, it has a similar efficacy profile but may differ in pharmacokinetic properties, allowing once‑daily dosing in most patients.

Store the tablets at ambient temperature, preferably below 25 °C, in the original packaging to protect them from moisture and light. Keep the product out of reach of children and do not use if the packaging is damaged or the tablets appear discolored.

Lercanidipin Actavis 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 unless specifically instructed by a healthcare professional.

Serious adverse events, although rare, include severe hypotension, angioedema (swelling of the face, lips, tongue or throat), and myocardial infarction. Patients should seek immediate medical attention if they experience fainting, pronounced swelling, chest pain, or any signs of an allergic reaction.

Lercanidipine is contraindicated in patients with known hypersensitivity to the drug or any component of the formulation, and in those with severe aortic stenosis or uncontrolled heart failure. Caution is also advised for individuals with significant hepatic impairment or low baseline blood pressure.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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