Product image of Lercanidipină Gemax Pharma (Lercanidipine Hydrochloride) supplied by GNH India

Lercanidipină Gemax Pharma

Active Ingredient:
Lercanidipine Hydrochloride
Origin:
EU

Lercanidipină Gemax Pharma (Lercanidipine Hydrochloride)

Lercanidipine, the active ingredient in Lercanidipine Gemax Pharma, is a dihydropyridine calcium channel blocker presented as a tablet for oral use. It is used to lower elevated blood pressure in adult patients.

GNH India supplies Lercanidipine Gemax Pharma as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Gemax Pharma S.R.O.

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Indications & Clinical Uses

Lercanidipine is indicated for the management of arterial hypertension, acting on the vascular smooth‑muscle calcium channels to lower blood pressure.

  • Essential hypertension: reduces systolic and diastolic blood pressure in adults.
  • Isolated systolic hypertension: provides effective control of elevated systolic pressure.
  • Secondary hypertension (renovascular, endocrine): used as part of combination therapy to achieve target pressures.

How It Works

  • Lercanidipine selectively blocks L-type calcium channels in vascular smooth muscle, inhibiting calcium influx that is required for contraction. This results in arterial vasodilation, decreased peripheral vascular resistance, and consequently 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.
  • Flushing: warm sensation, often on the face.
  • Peripheral edema: swelling of ankles or feet.
  • Dizziness or light‑headedness.
  • Tachycardia: increased heart rate.
  • Fatigue: general feeling of tiredness.

Serious or Rare Side Effects

  • Angioedema: swelling of lips, tongue, or airway.
  • Severe hypotension: marked drop in blood pressure causing syncope.
  • Myocardial infarction: rare occurrence in susceptible patients.
  • Hepatic injury: elevated liver enzymes or hepatitis.
  • Severe allergic reaction: rash, hives, or anaphylaxis.

Precautions & Warnings

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

  • Blood pressure monitoring: check regularly to avoid excessive hypotension.
  • Hepatic impairment: use with caution; dose adjustment may be required.
  • Concomitant antihypertensives: assess for additive blood‑pressure lowering effects.
  • Cardiovascular disease: evaluate for underlying ischemic heart disease.
  • Pregnancy and lactation: safety not established; avoid unless clearly needed.
  • Store at below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Lercanidipine can interact with several drug classes, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): increase plasma levels.
  • Grapefruit juice: may raise drug concentration.
  • Other calcium‑channel blockers: additive vasodilatory effect leading to hypotension.
  • Rifampicin or other CYP3A4 inducers: reduce therapeutic effect.
  • Concurrent use with antihypertensive agents that cause profound hypotension.

Moderate Interactions (Monitor Closely):\n- Diuretics: may enhance blood‑pressure reduction.

  • Beta‑blockers: monitor heart rate and blood pressure.
  • ACE inhibitors or ARBs: watch for excessive blood‑pressure lowering.
  • NSAIDs: may blunt antihypertensive response.
  • Lipid‑lowering agents (e.g., statins metabolized by CYP3A4): monitor for increased statin levels.

Frequently Asked Questions

Lercanidipine Gemax Pharma is used to treat hypertension. It belongs to the dihydropyridine calcium‑channel blocker class and helps lower elevated systolic and diastolic blood pressure in adult patients, reducing the risk of cardiovascular complications associated with high blood pressure.

Lercanidipine blocks L‑type calcium channels in the smooth muscle of arteries. By preventing calcium entry, it relaxes vascular smooth muscle, causing arterial vasodilation and a decrease in peripheral resistance, which leads to a reduction in systemic blood pressure.

The appropriate dose of lercanidipine is determined by the prescribing healthcare professional based on the individual’s clinical condition, response to therapy, and any concomitant medications. 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, and the product is classified as having an unknown pregnancy category. 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.

Both lercanidipine and amlodipine are dihydropyridine calcium‑channel blockers used for hypertension. Lercanidipine has a longer half‑life and may provide smoother blood‑pressure control with a lower incidence of peripheral edema in some patients, while amlodipine is more widely studied and available in many formulations.

Lercanidipine tablets should be stored at temperatures below 25 °C, in their original packaging, and protected from moisture and direct sunlight. Do not store in humid environments or expose the tablets to excessive heat, as this may affect product stability.

Lercanidipine 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 and not crush or chew the tablet.

Serious risks, although rare, include severe hypotension, angioedema, myocardial infarction, and hepatic injury. Patients should seek immediate medical attention if they experience swelling of the face or throat, sudden chest pain, fainting, or signs of liver dysfunction such as jaundice.

Lercanidipine is contraindicated in patients with known hypersensitivity to the drug or any component of the formulation. It should also be avoided in individuals with severe aortic stenosis, unstable angina, or those taking strong CYP3A4 inhibitors without appropriate medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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