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

Lercanidipine Teva

Active Ingredient:
Lercanidipine Hydrochloride
Origin:
EU

Lercanidipine Teva (Lercanidipine Hydrochloride)

Lercanidipine, the active ingredient in Lercanidipine Teva, is a calcium channel blocker presented as a tablet for oral use. It lowers blood pressure in adults with hypertension.

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

Manufacturer / TM Owner

Ratiopharm Gmbh

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Indications & Clinical Uses

Lercanidipine is a dihydropyridine calcium channel blocker used to manage elevated arterial pressure.

  • Hypertension: reduces systolic and diastolic blood pressure in patients with essential hypertension.
  • Isolated systolic hypertension: helps control high systolic readings in older adults.
  • Cardiovascular risk management: contributes to overall risk reduction when combined with lifestyle measures.

How It Works

  • Lercanidipine selectively inhibits L-type calcium channels in vascular smooth muscle, preventing calcium influx that is necessary for contraction. This vasodilatory effect decreases peripheral vascular resistance, leading to a reduction in systemic blood pressure without significant negative inotropic activity on the heart.

Side Effects

Lercanidipine is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Flushing: transient warmth and redness.
  • Peripheral edema: swelling of ankles or feet.
  • Dizziness: especially upon standing.
  • Tachycardia: increased heart rate.
  • Fatigue: feeling of tiredness.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure.
  • Angioedema: swelling of face, lips, or throat.
  • Myocardial infarction: rare occurrence of heart attack.
  • Hepatic enzyme elevation: abnormal liver function tests.
  • Allergic reactions: rash, pruritus, or anaphylaxis.
  • Cardiac conduction disturbances: heart block or arrhythmias.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient-specific factors and monitor for potential complications.

  • Blood pressure monitoring: check regularly to avoid excessive hypotension.
  • Liver function: assess baseline hepatic enzymes and monitor during treatment.
  • Concomitant antihypertensives: adjust doses to prevent additive blood pressure lowering.
  • Elderly patients: start at lower dose and titrate cautiously.
  • Pregnancy and lactation: use only if clearly needed, as safety data are limited.
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Lercanidipine may interact with other medicines that affect its metabolism or blood pressure effects.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase plasma concentrations.
  • Other antihypertensives (e.g., ACE inhibitors, diuretics): risk of excessive hypotension.
  • Grapefruit juice: can raise drug exposure and heighten side‑effect risk.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce efficacy.
  • NSAIDs: may increase risk of peripheral edema.
  • Beta‑blockers: can mask tachycardia that signals low blood pressure.
  • Lipid‑lowering agents (e.g., statins): may modestly raise statin levels.
  • Diuretics: monitor electrolytes and renal function.

Frequently Asked Questions

Lercanidipine Teva is prescribed to lower high blood pressure in adults diagnosed with hypertension. By reducing arterial pressure, it helps lower the risk of cardiovascular complications such as stroke and heart attack when used as part of a comprehensive treatment plan.

Lercanidipine blocks L-type calcium channels in the smooth muscle of blood vessels. This inhibition prevents calcium‑driven contraction, causing the vessels to relax and widen (vasodilation), which lowers peripheral resistance and consequently reduces systemic blood pressure.

The appropriate dose of lercanidipine is determined by the prescribing clinician based on the patient’s individual health status, blood pressure readings, and response to therapy. Patients should follow the dosage 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 any possible 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.

Lercanidipine belongs to the dihydropyridine calcium‑channel blocker class, which primarily causes arterial vasodilation. Compared with ACE inhibitors or beta‑blockers, it has a lower incidence of cough but may be more likely to cause peripheral edema. Choice of therapy depends on patient profile and comorbidities.

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

Lercanidipine Teva 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 instructed by a healthcare professional.

Serious adverse events, though rare, include severe hypotension, angioedema, myocardial infarction, and significant liver enzyme elevations. Patients should seek immediate medical attention if they experience swelling of the face or throat, sudden dizziness, chest pain, or signs of liver dysfunction.

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 dose adjustment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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