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

Lercadip

Active Ingredient:
Lercanidipine Hydrochloride
Origin:
EU

Lercadip (Lercanidipine Hydrochloride)

Lercanidipine, the active ingredient in Lercadip, 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 Lercadip as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Casen Recordati, S.L.

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Indications & Clinical Uses

Lercadip, a dihydropyridine calcium channel blocker, is used to manage conditions within the hypertension disease family.

  • Essential hypertension: reduces systolic and diastolic blood pressure, helping to prevent cardiovascular complications.
  • Isolated systolic hypertension: lowers elevated systolic pressure, improving vascular compliance.
  • Secondary hypertension (when caused by vascular resistance): assists in controlling pressure when other causes are addressed.

How It Works

  • Lercanidipine selectively blocks L‑type calcium channels on vascular smooth‑muscle cells, inhibiting calcium influx. This causes dose‑dependent relaxation of arterial smooth muscle, leading to vasodilation, reduced peripheral resistance, and consequently lower arterial blood pressure without significant negative inotropic effects on the heart.

Side Effects

Lercadip may be associated with a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Headache: mild to moderate intensity, often transient.
  • Flushing: warmth and redness, typically occurring shortly after dosing.
  • Peripheral edema: swelling of ankles or feet due to fluid accumulation.
  • Dizziness: sensation of light‑headedness, especially when standing quickly.
  • Fatigue: generalized tiredness without obvious cause.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure that may cause fainting.
  • Angioedema: rapid swelling of face, lips, tongue, or throat requiring urgent care.
  • Myocardial infarction: rare occurrence of heart attack symptoms.
  • Hepatic dysfunction: abnormal liver enzyme elevations.
  • Allergic reaction: rash, itching, or bronchospasm indicating hypersensitivity.

Precautions & Warnings

Before initiating therapy with Lercadip, several safety considerations should be observed.

  • Monitor blood pressure: ensure target levels are achieved and adjust dose if needed.
  • Avoid abrupt discontinuation: taper under medical supervision to prevent rebound hypertension.
  • Caution in hepatic impairment: reduced metabolism may increase exposure.
  • Use with caution in elderly patients: increased sensitivity to vasodilatory effects.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Lercadip can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may raise plasma concentrations and increase risk of hypotension.
  • Co‑administration with other potent antihypertensives (e.g., ACE inhibitors, beta‑blockers): can cause additive blood‑pressure lowering effects.
  • Grapefruit juice: can inhibit metabolism and elevate drug levels.

Moderate Interactions (Monitor Closely):\n- CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce therapeutic effect.

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may increase risk of renal impairment.
  • Diuretics: may enhance hypotensive response, requiring closer blood‑pressure monitoring.

Frequently Asked Questions

Lercadip contains lercanidipine hydrochloride, a calcium‑channel blocker indicated for the treatment of hypertension. By relaxing arterial smooth muscle, it helps lower elevated blood pressure and reduces the risk of cardiovascular events in adult patients.

Lercanidipine selectively blocks L‑type calcium channels on vascular smooth‑muscle cells, preventing calcium entry that is required for contraction. This results in vasodilation, decreased peripheral resistance, and a subsequent reduction in systemic 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 therapies. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

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 professional.

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.

Lercadip belongs to the dihydropyridine calcium‑channel blocker class, offering potent arterial vasodilation with a relatively low incidence of reflex tachycardia. Compared with ACE inhibitors or beta‑blockers, it may be preferred when patients experience cough or bronchospasm, but choice depends on individual clinical factors.

Lercadip tablets should be stored at room temperature, below 25 °C, in the original packaging to protect from moisture and light. Keep the container tightly closed and out of reach of children.

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

Serious adverse events, although rare, include severe hypotension, angioedema, myocardial infarction, and hepatic dysfunction. Patients should seek immediate medical attention if they experience sudden dizziness, swelling of the face or throat, chest pain, or jaundice.

Lercadip is contraindicated in patients with known hypersensitivity to lercanidipine or any component of the formulation, and in those with severe aortic stenosis or unstable heart failure. Clinicians should also exercise caution in patients with significant liver impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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