Product image of Lercadip (Lercanidipine Hydrochloride) supplied by GNH India

Lercadip

Active Ingredient:
Lercanidipine Hydrochloride
Origin:
EU

Lercadip (Lercanidipine Hydrochloride)

Lercanidipine Hydrochloride, the active ingredient in Lercadip, is a calcium channel blocker presented as an oral tablet for oral use. It treats hypertension in adult patients by relaxing vascular smooth muscle and reducing peripheral resistance.
GNH India supplies Lercadip as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Innova Pharma S.P.A.

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Indications & Clinical Uses

Lercanidipine Hydrochloride is a dihydropyridine calcium channel blocker used in the management of hypertension.

  • Hypertension: lowers systolic and diastolic blood pressure, improving cardiovascular risk profile.

How It Works

  • Lercanidipine Hydrochloride selectively blocks L‑type calcium channels on vascular smooth muscle cells. Inhibition of calcium influx prevents contraction, leading to vasodilation of peripheral arteries, decreased systemic vascular resistance, and consequently reduced arterial blood pressure. The drug’s high lipophilicity allows prolonged action and smooth muscle selectivity, minimizing direct cardiac effects.

Side Effects

Lercadip may cause a range of adverse reactions, from mild to serious.

Common Side Effects

  • Headache: mild to moderate intensity, often transient.
  • Flushing: sensation of warmth and redness, especially after the first dose.
  • Peripheral edema: swelling of ankles or lower limbs due to fluid accumulation.
  • Dizziness: light‑headed feeling, particularly when standing quickly.
  • Tachycardia: increased heart rate without other cardiac pathology.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure leading to fainting.
  • Angioedema: swelling of face, lips, tongue, or throat requiring urgent care.
  • Hepatic enzyme elevation: abnormal liver function tests indicating possible liver stress.
  • Myocardial infarction: rare occurrence of heart attack in susceptible individuals.
  • Life‑threatening arrhythmias: irregular heart rhythms that may require medical intervention.

Precautions & Warnings

Before prescribing Lercadip, clinicians should consider several safety measures.

  • Blood pressure monitoring: ensure adequate control and avoid excessive drops.
  • Hepatic impairment: dose adjustment may be needed in patients with liver dysfunction.
  • Elderly patients: start with the lowest effective dose and monitor for orthostatic effects.
  • Concomitant antihypertensives: watch for additive hypotensive effects when combined with other agents.
  • CYP3A4 inhibitors: avoid strong inhibitors that can increase lercanidipine plasma levels.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Lercadip can interact with several medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may raise lercanidipine concentrations and increase toxicity.
  • Grapefruit juice: can markedly elevate plasma levels, leading to excessive hypotension.
  • Other potent vasodilators (e.g., nitroglycerin): risk of severe blood pressure fall.

Moderate Interactions (Monitor Closely)

  • Diuretics: may enhance antihypertensive effect and electrolyte disturbances.
  • Beta‑blockers: combined use can cause additive heart rate reduction.
  • Digoxin: monitor for signs of digoxin toxicity due to altered renal clearance.
  • NSAIDs: may blunt antihypertensive response and affect renal function.

Frequently Asked Questions

Lercadip contains lercanidipine hydrochloride, which is prescribed to lower high blood pressure (hypertension) in adult patients. By relaxing the smooth muscle in blood vessels, it helps achieve and maintain target blood pressure levels, reducing the risk of cardiovascular complications.

Lercanidipine blocks L‑type calcium channels on vascular smooth‑muscle cells. This inhibition prevents calcium‑induced contraction, causing arterial vasodilation, lowering peripheral resistance, and ultimately reducing systolic and diastolic blood pressure.

The appropriate dose of Lercadip is determined by the prescribing clinician based on the individual’s blood‑pressure profile, age, renal and hepatic function, and concomitant medications. Patients should follow the specific 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 a qualified healthcare provider.

To place an order, visit the product page on gnhindia.com, submit an enquiry with the required quantity, and provide institutional or trade credentials. GNH India’s team will respond with pricing, availability, shipping details, and any necessary import documentation.

Lercadip belongs to the dihydropyridine calcium‑channel blocker class, offering once‑daily dosing and a favorable side‑effect profile compared with some older agents. Compared with ACE inhibitors or ARBs, it primarily reduces vascular resistance without directly affecting the renin‑angiotensin system.

Lercadip tablets should be stored at temperatures below 25 °C, in their original container, protected from moisture and direct sunlight. Do not store in bathrooms or near heat sources to maintain product stability.

Lercadip is taken orally, usually once daily, with or without food, as directed by a healthcare professional. Swallow the tablet whole with a glass of water; do not crush or chew unless specifically instructed.

Serious adverse events, though rare, include severe hypotension, angioedema, significant liver enzyme elevations, myocardial infarction, and life‑threatening arrhythmias. Patients should seek immediate medical attention if they experience swelling of the face or throat, chest pain, or fainting.

Lercadip is contraindicated in patients with known hypersensitivity to lercanidipine or other dihydropyridine calcium‑channel blockers, and in those with severe aortic stenosis or unstable angina. Caution is also advised for individuals with significant hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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