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

Lercanidipina Ratiopharm Italia

Active Ingredient:
Lercanidipine Hydrochloride
Origin:
EU

Lercanidipina Ratiopharm Italia (Lercanidipine Hydrochloride)

Lercanidipine, the active ingredient in Lercanidipina Ratiopharm Italia, is a calcium channel blocker presented as an oral tablet for oral use. It treats hypertension by relaxing arterial smooth muscle and is prescribed for adult patients with elevated blood pressure.

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

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

  • Lercanidipine is a calcium channel blocker used to manage conditions that involve high arterial pressure.
  • Hypertension: reduces systolic and diastolic blood pressure, helping to lower the risk of cardiovascular events.

How It Works

  • Lercanidipine selectively inhibits L‑type calcium channels in vascular smooth muscle cells. By blocking calcium influx, it prevents contraction of arterial smooth muscle, leading to vasodilation of peripheral arteries. The resulting decrease in systemic vascular resistance lowers arterial blood pressure without significant effect on heart rate or cardiac output.

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: warmth and redness of the skin.
  • Peripheral edema: swelling of the ankles or lower legs.
  • Dizziness: especially upon standing.
  • Tiredness: general feeling of fatigue.
  • Nasal congestion: blocked or runny nose.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure.
  • Angio‑edema: rapid swelling of face, lips, or throat.
  • Hepatic dysfunction: abnormal liver enzyme levels.
  • Cardiac arrhythmia: irregular heart rhythm.
  • Allergic reaction: rash, itching, or anaphylaxis.
  • Myocardial infarction: rare occurrence of heart attack.

Precautions & Warnings

  • Before initiating therapy with lercanidipine, consider the following safety measures.
  • Pregnancy: avoid use unless clearly needed; discuss risks with a healthcare professional.
  • Breastfeeding: assess benefit‑risk ratio; drug may pass into milk.
  • Severe hepatic impairment: dose adjustment may be required.
  • Concomitant use with strong CYP3A4 inhibitors: monitor for increased exposure.
  • Elderly patients: start at low dose and titrate cautiously.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and light.

Avoid Interactions

Lercanidipine can interact with several medicines, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may raise plasma levels and increase risk of hypotension.
  • Grapefruit juice: can markedly increase drug concentration.
  • Other antihypertensives: additive blood‑pressure lowering effect may cause severe hypotension.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce effectiveness.
  • Diuretics: may enhance electrolyte disturbances.
  • Beta‑blockers: monitor heart rate and blood pressure.
  • NSAIDs: may attenuate antihypertensive response.
  • Lipid‑lowering agents (e.g., statins metabolised by CYP3A4): watch for increased statin levels.

Frequently Asked Questions

Lercanidipina Ratiopharm Italia 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 the risk of cardiovascular complications in adult patients.

Lercanidipine selectively blocks L‑type calcium channels in vascular smooth muscle. This inhibition prevents calcium‑mediated contraction, causing peripheral arterial vasodilation and a consequent reduction in systemic vascular resistance and blood pressure.

The appropriate dose of lercanidipine is determined by the prescribing clinician based on the individual’s medical condition, response to therapy, and any concomitant medications. Patients should follow the dosage instructions provided by their healthcare professional.

Safety of lercanidipine in pregnancy has not been fully established; it should only be used if the potential benefit justifies the potential risk to the fetus. During breastfeeding, the drug may be excreted in milk, so a risk‑benefit assessment is required.

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 arterial vasodilation with a relatively low effect on heart rate. Compared with ACE inhibitors or ARBs, it may cause fewer cough-related side effects but can be associated with peripheral edema.

Lercanidipina Ratiopharm Italia should be stored at ambient temperature, preferably below 25 °C. Keep the tablets in the original blister pack, protect them from moisture and direct sunlight, and ensure they are out of reach of children.

Lercanidipine is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with a glass of water and not chewed or crushed, unless otherwise directed by a healthcare professional.

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

Lercanidipine is contraindicated in patients with known hypersensitivity to the drug or any component of the formulation, and in individuals with severe aortic stenosis or unstable angina. Caution is advised for patients with significant hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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