Product image of Lercanidipino Tarbis (Lercanidipine Hydrochloride Hemihydrate) supplied by GNH India

Lercanidipino Tarbis

Active Ingredient:
Lercanidipine Hydrochloride Hemihydrate
Origin:
EU

Lercanidipino Tarbis (Lercanidipine Hydrochloride Hemihydrate)

Lercanidipine, the active ingredient in Lercanidipino Tarbis, is a calcium channel blocker presented as a tablet for oral use. It lowers elevated blood pressure in adults with hypertension. GNH India supplies Lercanidipino Tarbis as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Tarbis Farma, S.L.

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Indications & Clinical Uses

Lercanidipine is indicated for the management of hypertension, acting on vascular smooth muscle to reduce systemic vascular resistance.

  • Essential hypertension: lowers systolic and diastolic blood pressure in patients with primary high blood pressure.
  • Isolated systolic hypertension: reduces elevated systolic pressure, particularly in older adults.
  • Secondary hypertension: assists in controlling blood pressure when caused by other underlying conditions.

How It Works

  • Lercanidipine selectively blocks L-type calcium channels in vascular smooth muscle cells, inhibiting calcium influx. This leads to relaxation of arterial smooth muscle, vasodilation, and a consequent decrease in peripheral vascular resistance, which lowers systemic blood pressure.

Side Effects

Adverse reactions may occur with Lercanidipine therapy.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Flushing: transient warmth and redness of the skin.
  • Peripheral edema: swelling of the ankles or lower legs.
  • Dizziness: especially upon standing.
  • Tachycardia: increased heart rate.
  • Nausea: occasional stomach upset.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure requiring medical attention.
  • Myocardial infarction: rare occurrence of heart attack.
  • Hepatic dysfunction: abnormal liver enzyme elevations.
  • Allergic reactions: including angioedema or rash.
  • Cardiac arrhythmia: irregular heart rhythms.
  • Stevens‑Johnson syndrome: severe skin reaction.

Precautions & Warnings

When prescribing Lercanidipine, clinicians should consider several safety measures.

  • Blood pressure monitoring: regularly assess to avoid excessive hypotension.
  • Liver function assessment: evaluate hepatic status before initiation.
  • Elderly patients: start at lower doses due to increased sensitivity.
  • Concomitant vasodilators: avoid abrupt combination that may cause profound hypotension.
  • Discontinuation: taper gradually rather than stopping suddenly.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Lercanidipine may interact with other medicines; awareness of interaction severity is essential.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase plasma levels.
  • Grapefruit juice: can elevate drug concentration.
  • Concurrent potent vasodilators: risk of severe hypotension.

Moderate Interactions (Monitor Closely):\n- Other antihypertensives (beta‑blockers, ACE inhibitors): may enhance blood‑pressure‑lowering effect.

  • Diuretics: can potentiate orthostatic hypotension.
  • NSAIDs: may reduce antihypertensive efficacy.
  • Digoxin: possible increase in serum digoxin levels.

Frequently Asked Questions

Lercanidipino Tarbis contains lercanidipine, a calcium‑channel‑blocking agent prescribed to lower high blood pressure in adults with hypertension. By relaxing arterial smooth muscle, it helps achieve target blood‑pressure levels and reduces cardiovascular risk associated with sustained hypertension.

Lercanidipine selectively inhibits L‑type calcium channels on vascular smooth‑muscle cells, preventing calcium entry that is necessary for muscle contraction. This causes arterial dilation, decreases peripheral vascular resistance, and ultimately lowers systemic blood pressure.

The appropriate dose of Lercanidipino Tarbis is determined by the prescribing clinician based on the patient’s clinical condition, blood‑pressure response, and any concomitant therapies. Dosage adjustments are made according to individual therapeutic needs.

Safety data for lercanidipine in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To request Lercanidipino Tarbis, 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 ACE inhibitors or beta‑blockers, it may cause fewer cough or fatigue symptoms but can be associated with peripheral edema. Choice of therapy depends on patient profile and comorbidities.

Lercanidipino Tarbis should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight, and excessive heat to maintain its stability and potency.

Lercanidipino Tarbis is taken orally, usually once daily, with or without food, as directed by the prescribing physician. The tablet should be swallowed whole with a glass of water and not chewed or crushed.

Serious adverse events, although rare, include severe hypotension, myocardial infarction, hepatic dysfunction, allergic reactions such as angioedema, and life‑threatening skin conditions like Stevens‑Johnson syndrome. Patients should seek immediate medical attention if they experience any of these symptoms.

Lercanidipino Tarbis is contraindicated in patients with known hypersensitivity to lercanidipine or any component of the formulation. Caution is advised for individuals with severe hepatic impairment, unstable angina, or those taking strong CYP3A4 inhibitors, unless a healthcare professional determines it is appropriate.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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