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

Lerkanidipin Actavis

Active Ingredient:
Lercanidipine Hydrochloride
Origin:
EU

Lerkanidipin Actavis (Lercanidipine Hydrochloride)

Lercanidipine hydrochloride, the active ingredient in Lerkanidipin Actavis, is a calcium channel blocker presented as an oral tablet for oral use. It is prescribed to manage hypertension in adult patients and to reduce cardiovascular risk and to reduce cardiovascular risk. It is prescribed under physician supervision through its vasodilatory action in the arterial system.

GNH India supplies Lerkanidipin Actavis as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation for export to multiple regions.

Manufacturer / TM Owner

Actavis Group Ptc Ehf.

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Indications & Clinical Uses

Lercanidipine is a calcium channel blocker used in the management of high‑blood‑pressure conditions.

  • Essential hypertension: lowers systolic and diastolic blood pressure, helping to prevent stroke and heart attack.
  • Isolated systolic hypertension: reduces elevated systolic pressure, particularly in older adults.
  • Hypertension in elderly patients: provides effective blood pressure control with a favorable tolerability profile.

How It Works

  • Lercanidipine hydrochloride selectively blocks L-type calcium channels in vascular smooth muscle, inhibiting calcium influx. This results in relaxation of arterial smooth muscle, leading to vasodilation, decreased peripheral vascular resistance, and ultimately a reduction in systemic blood pressure without significant effect on cardiac conduction.

Side Effects

Lercanidipine may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Headache: mild to moderate pain often occurring after the first dose.
  • Flushing: sensation of warmth and redness, typically on the face or neck.
  • Peripheral edema: swelling of the ankles or feet due to fluid accumulation.
  • Dizziness: light‑headed feeling, especially when standing quickly.
  • Fatigue: general tiredness that may improve with continued therapy.
  • Tachycardia: increased heart rate, usually mild.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure causing fainting or shock.
  • Myocardial infarction: rare occurrence of heart attack, particularly in patients with existing coronary disease.
  • Arrhythmias: abnormal heart rhythms that may require medical attention.
  • Hepatic injury: signs of liver dysfunction such as jaundice or elevated enzymes.
  • Allergic reactions: rash, itching, swelling, or difficulty breathing indicating possible anaphylaxis.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety aspects.

  • Blood pressure monitoring: ensure adequate control and avoid excessive hypotension.
  • Hepatic impairment: use caution and consider dose adjustment in patients with liver dysfunction.
  • Elderly patients: start at the lowest effective dose and monitor for dizziness or falls.
  • Concomitant antihypertensives: assess for additive blood‑pressure‑lowering effects.
  • Severe aortic stenosis: contraindicated due to risk of precipitating cardiac failure.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Lercanidipine can interact with several drug classes, influencing its efficacy and safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase plasma concentrations and risk of hypotension.
  • Grapefruit juice: can markedly raise lercanidipine levels, leading to enhanced adverse effects.
  • Other potent antihypertensives: may cause additive blood‑pressure reduction and syncope.

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

  • Diuretics: can potentiate orthostatic hypotension; monitor electrolytes and blood pressure.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may attenuate antihypertensive response; assess renal function regularly.

Frequently Asked Questions

Lerkanidipin Actavis contains lercanidipine hydrochloride, which is prescribed to treat hypertension. By lowering elevated blood pressure, it helps reduce the risk of cardiovascular events such as stroke and heart attack in adult patients.

Lercanidipine blocks L-type calcium channels in arterial smooth muscle, preventing calcium entry that causes contraction. This leads to vasodilation, decreased peripheral resistance, and a subsequent reduction in systemic blood pressure.

The appropriate dose of Lerkanidipin Actavis is determined by a qualified prescriber based on the individual’s clinical condition, response to therapy, and any concomitant medications. Patients should follow the dosing instructions provided by their healthcare professional.

Safety data for lercanidipine in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by the prescribing clinician.

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, offering potent arterial vasodilation with a relatively long half‑life. Compared with amlodipine, it may provide a smoother blood‑pressure profile and lower incidence of peripheral edema, though individual response varies.

Store the tablets at room temperature, below 25 °C, in the original blister pack. Keep them away from moisture, heat, and direct sunlight to maintain potency throughout the shelf life.

Lerkanidipin Actavis is taken orally, usually once daily with or without food. The tablet should be swallowed whole with a glass of water and not crushed or chewed.

Serious adverse events, though rare, include severe hypotension, myocardial infarction, significant arrhythmias, hepatic injury, and allergic reactions such as anaphylaxis. Patients should seek immediate medical attention if they experience symptoms like fainting, chest pain, or difficulty breathing.

Lerkanidipin Actavis is contraindicated in patients with known hypersensitivity to lercanidipine or any component of the formulation, and in those with severe aortic stenosis. Caution is also advised for individuals with significant liver impairment or uncontrolled heart failure.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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