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

Lercanidipin-Hcl Stada

Active Ingredient:
Lercanidipine Hydrochloride
Origin:
EU

Lercanidipin-Hcl Stada (Lercanidipine Hydrochloride)

Lercanidipine hydrochloride, the active ingredient in Lercanidipin-Hcl Stada, is a calcium channel blocker presented as a tablet for oral use. It treats hypertension in adult patients by lowering elevated blood pressure. GNH India supplies Lercanidipin-Hcl Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Stadapharm Gmbh

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Indications & Clinical Uses

  • Lercanidipine hydrochloride is used to manage hypertension, a condition characterized by chronically elevated arterial pressure.
  • Hypertension: reduces systolic and diastolic blood pressure, helping to lower the risk of cardiovascular events.
  • Essential hypertension: provides long‑term blood pressure control in primary hypertension.
  • High blood pressure: assists in achieving target blood pressure goals as part of antihypertensive therapy.

How It Works

  • Lercanidipine hydrochloride selectively blocks L‑type calcium channels in vascular smooth muscle. Inhibition of calcium influx prevents contraction of arterial smooth muscle, leading to vasodilation of peripheral vessels. The resulting decrease in systemic vascular resistance lowers arterial pressure, providing antihypertensive effect without significant negative inotropic activity.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate intensity, often transient.
  • Flushing: sensation of warmth and redness, especially on the face.
  • Peripheral edema: swelling of ankles or lower legs.
  • Dizziness or light‑headedness, particularly after standing.
  • Tachycardia: increased heart rate in some patients.
  • Gastrointestinal discomfort: nausea or abdominal pain.

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 angioedema.
  • Cardiac arrhythmias: abnormal heart rhythms.
  • Stevens‑Johnson syndrome: rare severe skin reaction.

Precautions & Warnings

  • Before initiating therapy with lercanidipine, clinicians should consider several safety aspects.
  • Monitor blood pressure: adjust dose based on therapeutic response.
  • Avoid abrupt discontinuation: taper to prevent rebound hypertension.
  • Caution in hepatic impairment: dose may need adjustment.
  • Use carefully in elderly patients: increased sensitivity to hypotension.
  • Avoid concomitant strong CYP3A4 inhibitors: may raise drug levels.
  • Store at ambient temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase plasma concentrations.
  • Co‑administration with other antihypertensives: risk of excessive hypotension.
  • Grapefruit juice: can elevate drug exposure.
  • Simultaneous use with diltiazem or verapamil: additive calcium‑channel blockade.
  • Rifampicin: may reduce therapeutic effect.

Moderate Interactions (Monitor Closely)

  • Diuretics: monitor electrolytes and blood pressure.
  • Beta‑blockers: may require dose adjustments.
  • NSAIDs: can attenuate antihypertensive response.
  • Antidiabetic agents: monitor glucose control.
  • Lipid‑lowering statins: observe for muscle toxicity.

Frequently Asked Questions

Lercanidipin-Hcl Stada contains lercanidipine hydrochloride, a calcium channel blocker indicated for the treatment of hypertension. It helps lower elevated blood pressure and reduces the risk of cardiovascular complications associated with high blood pressure.

Lercanidipine selectively blocks L‑type calcium channels in vascular smooth muscle. By preventing calcium entry, it relaxes arterial walls, causing vasodilation and a reduction in systemic vascular resistance, which leads to lower blood pressure.

The dosage of lercanidipine is individualized by the prescribing healthcare professional based on the patient’s blood pressure, response, and tolerability. The prescriber determines the appropriate strength and dosing schedule.

Safety of lercanidipine in pregnancy and lactation has not been fully 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 necessary import documentation.

Lercanidipine belongs to the dihydropyridine calcium‑channel blocker class, offering potent vasodilation with a relatively low incidence of reflex tachycardia compared with some non‑dihydropyridine agents. It is often used when patients need effective blood‑pressure control with once‑daily dosing, and may be combined with other classes for synergistic effect.

Lercanidipine tablets should be stored at ambient temperature, below 25 °C, in the original container to protect from moisture and light. Keep the product out of reach of children and avoid exposure to extreme humidity.

Lercanidipine is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with a glass of water and not chewed or crushed, unless otherwise directed by a healthcare professional.

Serious risks include severe hypotension, which can cause fainting or falls, and rare but serious reactions such as myocardial infarction, hepatic dysfunction, and severe allergic responses like angioedema or Stevens‑Johnson syndrome. Patients should seek immediate medical attention if they experience these symptoms.

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 cardiogenic shock. Caution is also advised for patients with significant liver impairment or those taking strong CYP3A4 inhibitors.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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