Product image of Lercanidipina Aurovitas (Lercanidipine Hydrochloride) supplied by GNH India

Lercanidipina Aurovitas

Active Ingredient:
Lercanidipine Hydrochloride
Origin:
EU

Lercanidipina Aurovitas (Lercanidipine Hydrochloride)

Lercanidipine, the active ingredient in Lercanidipina Aurovitas, is a calcium channel blocker presented as an oral tablet for oral use. It treats hypertension in adult patients by promoting vascular relaxation and lowering blood pressure.

GNH India supplies Lercanidipina Aurovitas as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Generis Farmacêutica, S.A.

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Indications & Clinical Uses

Lercanidipine is used to manage high blood pressure, acting on the vascular smooth‑muscle calcium channels that regulate tone.

  • Essential hypertension: reduces systolic and diastolic pressure in patients with primary high blood pressure.
  • Isolated systolic hypertension: lowers elevated systolic readings, especially in older adults.
  • General hypertension: helps achieve target blood pressure levels as part of antihypertensive therapy.

How It Works

  • Lercanidipine selectively inhibits L‑type calcium channels in vascular smooth muscle, decreasing calcium influx. This leads to relaxation of arterial smooth muscle, vasodilation, and a consequent reduction in peripheral vascular resistance, which lowers systemic blood pressure without significant effect on cardiac contractility.

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 with reddening of skin.
  • Peripheral edema: swelling of ankles or feet.
  • Dizziness: especially upon standing.
  • Tiredness: general feeling of fatigue.
  • Palpitations: awareness of heartbeat.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure requiring medical attention.
  • Angio‑edema: rapid swelling of face, lips, or throat.
  • Hepatic dysfunction: abnormal liver enzymes.
  • Allergic reactions: rash, itching, or anaphylaxis.
  • Cardiac arrhythmias: irregular heart rhythms.
  • Renal impairment: worsening kidney function.

Precautions & Warnings

Before initiating therapy, consider patient‑specific factors and monitor for potential risks.

  • Pregnancy: safety not established; avoid unless clearly needed.
  • Breastfeeding: unknown excretion; weigh benefits against risks.
  • Liver disease: use with caution; dose adjustment may be required.
  • Elderly: monitor for orthostatic hypotension and renal function.
  • Drug interactions: review concomitant medications for additive blood‑pressure effects.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase plasma levels and risk of hypotension.
  • Grapefruit juice: can elevate drug concentration leading to adverse effects.

Moderate Interactions (Monitor Closely):\n- Other antihypertensives (e.g., ACE inhibitors, diuretics): may cause additive blood‑pressure lowering.

  • Simvastatin or other CYP3A4 substrates: may increase statin exposure, raising myopathy risk.
  • Beta‑blockers: monitor for excessive bradycardia or hypotension.
  • NSAIDs: may attenuate antihypertensive effect.
  • Alcohol: can enhance vasodilatory effects, leading to dizziness.

Frequently Asked Questions

Lercanidipina Aurovitas contains lercanidipine, a calcium channel blocker indicated for the treatment of hypertension. It helps lower elevated blood pressure by relaxing arterial smooth muscle, thereby reducing vascular resistance and improving cardiovascular risk management.

Lercanidipine selectively blocks L‑type calcium channels in vascular smooth muscle cells. By limiting calcium entry, it prevents muscle contraction, causing vasodilation of peripheral arteries. This vasodilatory effect decreases systemic vascular resistance, leading to a reduction in systolic and diastolic blood pressure.

The appropriate dose of Lercanidipina Aurovitas is determined by a qualified prescriber based on the individual’s clinical condition, response to therapy, and any concomitant medications. Patients should follow the dosing instructions provided by their healthcare professional.

Safety of lercanidipine in pregnancy and lactation has not been established. It should be used only if the potential benefit justifies the potential risk to the fetus or infant, and decisions should be made in consultation with a 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 long half‑life. Compared with ACE inhibitors or beta‑blockers, it primarily reduces peripheral resistance and may cause fewer cough-related side effects, but it can be associated with peripheral edema.

Lercanidipina Aurovitas tablets should be stored at ambient temperature, below 25 °C, in their original packaging. Protect the product from moisture, direct sunlight, and extreme temperature fluctuations to maintain stability.

The medication 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 and do not crush or chew it unless specifically instructed.

Serious adverse events, though rare, include severe hypotension, angio‑edema, hepatic dysfunction, and significant cardiac arrhythmias. Patients should seek immediate medical attention if they experience sudden dizziness, swelling of the face or throat, or any signs of liver injury.

Individuals with known hypersensitivity to lercanidipine or any component of the formulation should avoid the product. Caution is also advised for patients with severe liver impairment, uncontrolled heart failure, or those taking strong CYP3A4 inhibitors without medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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