Product image of Lercanidipina Atral (Lercanidipine Hydrochloride) supplied by GNH India

Lercanidipina Atral

Active Ingredient:
Lercanidipine Hydrochloride
Origin:
EU

Lercanidipina Atral (Lercanidipine Hydrochloride)

Lercanidipine Hydrochloride, the active ingredient in Lercanidipina Atral, is a calcium channel blocker presented as an oral dosage form for oral use. It is employed to lower elevated blood pressure in adult patients with hypertension. The medication works by relaxing arterial smooth muscle, decreasing peripheral vascular resistance, and conforms to European Union quality standards and GMP manufacturing.

GNH India supplies Lercanidipina Atral as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. Our distribution network ensures reliable delivery to diverse healthcare settings across multiple continents.

Manufacturer / TM Owner

Laboratórios Atral, S.A.

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Indications & Clinical Uses

Lercanidipine is a calcium channel blocker used to manage hypertension, the primary disease pathway it influences.

  • Essential hypertension: lowers systolic and diastolic blood pressure in patients with primary hypertension.
  • Isolated systolic hypertension: reduces elevated systolic pressure, particularly in older adults.
  • Secondary hypertension (as adjunct therapy): contributes to blood pressure control when combined with other antihypertensives.

How It Works

  • Lercanidipine selectively blocks L‑type calcium channels in vascular smooth muscle cells, inhibiting calcium influx that is necessary for contraction. This antagonism leads to relaxation of arterial smooth muscle, resulting in vasodilation and a decrease in peripheral vascular resistance, which in turn lowers systemic blood pressure without significant effect on heart rate. The drug exhibits high affinity for arterial vessels while sparing venous capacitance vessels, providing a favorable hemodynamic profile.

Side Effects

Lercanidipine may be associated with a range of adverse reactions, which are categorized by frequency.

Common Side Effects

  • Headache: mild to moderate pain often occurring early in therapy.
  • Flushing: transient warmth and redness of the skin.
  • Peripheral edema: swelling of the lower limbs due to fluid accumulation.
  • Dizziness: sensation of light‑headedness, especially upon standing.

Serious or Rare Side Effects

  • Angioedema: rapid swelling of face, lips, tongue or airway requiring immediate medical attention.
  • Severe hypotension: marked drop in blood pressure that may cause fainting.
  • Myocardial infarction: rare occurrence of heart attack, particularly in patients with pre‑existing coronary disease.

Precautions & Warnings

Before initiating therapy with lercanidipine, several safety considerations should be reviewed.

  • Renal impairment: monitor kidney function and adjust therapy as needed.
  • Hepatic impairment: use with caution; dose adjustments may be required.
  • Concomitant CYP3A4 inhibitors: avoid or reduce dose due to increased plasma concentrations.
  • Pregnancy: safety not established; avoid unless benefits outweigh risks.
  • Elderly patients: start at low dose and monitor for orthostatic hypotension.
  • Store at ambient temperature: keep in original packaging, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may cause excessive hypotension.
  • Grapefruit juice: increases drug exposure and risk of adverse effects.
  • Combined use with other antihypertensives (e.g., ACE inhibitors, diuretics): may lead to additive blood pressure lowering.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce therapeutic effect.
  • Beta‑blockers: may mask tachycardia signs of hypotension.
  • Lithium: may increase serum lithium levels, requiring monitoring.

Frequently Asked Questions

Lercanidipina Atral contains the active ingredient lercanidipine hydrochloride, which is prescribed to lower elevated blood pressure in adults diagnosed with hypertension. By reducing peripheral vascular resistance, it helps achieve target blood pressure levels and lowers the risk of cardiovascular complications associated with uncontrolled hypertension.

Lercanidipine selectively blocks L‑type calcium channels on arterial smooth‑muscle cells. This inhibition prevents calcium‑dependent contraction, causing the arteries to relax and widen (vasodilation). The resulting decrease in peripheral vascular resistance leads to a reduction in systemic blood pressure without a pronounced effect on heart rate.

The appropriate dose of Lercanidipina Atral is determined by the prescribing healthcare professional based on the individual’s clinical condition, response to therapy, and any concomitant medications. Dosage adjustments may be required for specific patient groups such as the elderly or those with hepatic or renal impairment.

Safety data for lercanidipine during pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. It should only be used if the potential benefit justifies the potential risk to the fetus. Breastfeeding mothers should consult their physician before using the medication.

To place an order, submit an enquiry on the product page at gnhindia.com specifying the required quantity of Lercanidipina Atral. 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.

Both lercanidipine and amlodipine belong to the dihydropyridine class of calcium channel blockers and are used to treat hypertension. Lercanidipine has a longer half‑life and may provide smoother blood‑pressure control with once‑daily dosing, while amlodipine is more widely studied. Choice between them depends on individual patient response, tolerability and physician preference.

Lercanidipina Atral should be stored at ambient temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the product out of reach of children and do not use it after the expiry date indicated on the label.

Lercanidipina Atral is taken orally, usually once daily, with or without food as directed by the prescribing clinician. Tablets should be swallowed whole with a glass of water and not chewed or crushed unless specifically instructed.

Serious adverse events, although rare, include angioedema, severe hypotension that can lead to fainting, and myocardial infarction, particularly in patients with existing coronary artery disease. Immediate medical attention is required if any signs of swelling of the face, lips, tongue, or difficulty breathing occur.

Lercanidipina Atral should be avoided in patients with known hypersensitivity to lercanidipine or any other component of the formulation. Caution is also advised for individuals with severe hepatic impairment, uncontrolled heart failure, or those taking strong CYP3A4 inhibitors without appropriate dose adjustment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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