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

Lercanidipin Stada

Active Ingredient:
Lercanidipine Hydrochloride
Origin:
EU

Lercanidipin Stada (Lercanidipine Hydrochloride)

Lercanidipine, the active ingredient in Lercanidipin Stada, is a dihydropyridine calcium channel blocker presented as an oral tablet for systemic use. It is indicated for the management of elevated blood pressure in adults, particularly those with essential hypertension.

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

Manufacturer / TM Owner

Stada Arzneimittel Gmbh

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Indications & Clinical Uses

Lercanidipine is used to treat conditions within the hypertension disease family by relaxing vascular smooth muscle and lowering arterial pressure.

  • Essential hypertension: reduces systolic and diastolic blood pressure to target levels.
  • Isolated systolic hypertension: improves pulse pressure in older patients.
  • Hypertension in the elderly: provides effective blood pressure control with once‑daily dosing.

How It Works

  • Lercanidipine selectively blocks L‑type calcium channels in vascular smooth muscle, preventing calcium influx that is necessary for contraction. This inhibition leads to arterial vasodilation, decreased peripheral vascular resistance, and ultimately a reduction in systemic blood pressure without significant negative inotropic effects on the heart.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate intensity, often occurring early in therapy.
  • Flushing: warm sensation and reddening of the skin, usually transient.
  • Peripheral edema: swelling of the ankles or lower legs due to vasodilation.
  • Dizziness or light‑headedness, especially when standing quickly.
  • Tachycardia: increased heart rate as a reflex response.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure causing fainting.
  • Myocardial infarction: rare occurrence of heart attack.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Allergic reactions: rash, pruritus, or anaphylaxis in susceptible individuals.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for potential risks.

  • Blood pressure monitoring: assess baseline and periodic readings to avoid excessive hypotension.
  • Hepatic impairment: use with caution and consider dose adjustment in patients with liver disease.
  • Elderly patients: start at the lowest effective dose due to increased sensitivity.
  • Concomitant antihypertensives: watch for additive blood‑pressure‑lowering effects.
  • Discontinuation: avoid abrupt cessation to prevent rebound hypertension.
  • 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, itraconazole): may increase plasma concentrations.
  • Grapefruit juice: can markedly raise drug levels and risk of hypotension.
  • Other potent antihypertensives: additive blood‑pressure‑lowering effect leading to severe hypotension.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce therapeutic effect.
  • Beta‑blockers: may require careful titration to avoid excessive heart‑rate reduction.
  • Diuretics: monitor electrolytes and blood pressure for synergistic effects.

Frequently Asked Questions

Lercanidipin Stada contains lercanidipine hydrochloride, an oral antihypertensive medication. It is prescribed to lower elevated blood pressure in adults, primarily for essential hypertension, by relaxing the smooth muscle of blood vessels and reducing vascular resistance.

Lercanidipine selectively blocks L‑type calcium channels in arterial smooth muscle. This inhibition prevents calcium‑mediated contraction, leading to vasodilation, decreased peripheral resistance, and a subsequent reduction in systemic blood pressure.

The appropriate dose of lercanidipine is determined by the prescribing healthcare professional based on the patient’s clinical condition, response to therapy, and any concomitant medications. Dosage adjustments are individualized and should follow the prescriber’s instructions.

The safety of lercanidipine in pregnancy and lactation has not been established. 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 a qualified healthcare provider.

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, which primarily causes arterial vasodilation. Compared with ACE inhibitors or beta‑blockers, it has a lower incidence of cough but may be more associated with peripheral edema. Choice of therapy depends on patient profile and comorbidities.

Lercanidipin Stada tablets should be stored at room temperature, below 25 °C, in the original packaging to protect from moisture and light. Keep the product out of reach of children and do not use after the expiry date.

Lercanidipin Stada is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with a glass of water. Patients should follow the dosing schedule prescribed by their healthcare professional.

Serious risks, although rare, include severe hypotension, myocardial infarction, significant liver enzyme elevations, and allergic reactions such as rash or anaphylaxis. Patients should seek immediate medical attention if they experience symptoms like fainting, chest pain, or severe skin reactions.

Lercanidipine is contraindicated in patients with known hypersensitivity to the drug or any component of the formulation. Caution is advised in individuals with severe hepatic impairment, uncontrolled heart failure, 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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