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

Lercanidipin-Hcl Teva

Active Ingredient:
Lercanidipine Hydrochloride
Origin:
EU

Lercanidipin-Hcl Teva (Lercanidipine Hydrochloride)

Lercanidipine hydrochloride, the active ingredient in Lercanidipin-Hcl Teva, is a calcium channel blocker presented as a tablet for oral use. It is available in the European Union market and formulated to provide consistent bioavailability, helping to treat hypertension in adult patients by lowering elevated blood pressure.

GNH India supplies Lercanidipin-Hcl Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to Good Distribution Practice and offers reliable logistics for global demand.

Manufacturer / TM Owner

Teva Gmbh

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Indications & Clinical Uses

  • Lercanidipine is a dihydropyridine calcium‑channel blocker indicated for the management of high‑blood‑pressure conditions.
  • Essential hypertension: reduces systolic and diastolic blood pressure in patients with primary hypertension.
  • Isolated systolic hypertension: provides effective control of elevated systolic pressure, especially in older adults.
  • Hypertension in the elderly: improves blood pressure control with a favorable tolerability profile in senior patients.

How It Works

  • Lercanidipine selectively inhibits L‑type calcium channels in vascular smooth‑muscle cells, preventing calcium influx that is necessary for contraction. This vasodilatory effect reduces peripheral vascular resistance, leading to a decrease in arterial blood pressure without significant impact on cardiac conduction or contractility. The drug’s high lipophilicity allows prolonged action and steady plasma levels.

Side Effects

Lercanidipine may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Headache: mild to moderate intensity, often transient.
  • Flushing: warm sensation and redness, usually temporary.
  • Peripheral edema: swelling of ankles or lower legs.
  • Dizziness: sensation of light‑headedness, especially after standing.
  • Tachycardia: increased heart rate without other cardiac symptoms.
  • Palpitations: awareness of heart beating faster or irregularly.

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips, tongue, or throat requiring immediate medical attention.
  • Severe hypotension: marked drop in blood pressure causing faintness or shock.
  • Myocardial infarction: rare occurrence of heart attack symptoms.
  • Hepatic dysfunction: abnormal liver enzymes or hepatitis.
  • Allergic reactions: rash, itching, or urticaria.
  • Stevens‑Johnson syndrome: severe skin reaction, requires urgent care.

Precautions & Warnings

  • When prescribing lercanidipine, clinicians should consider several safety precautions to minimize risk.
  • Blood pressure monitoring: check blood pressure regularly after initiation and dose adjustments.
  • Hepatic impairment: use with caution in patients with moderate to severe liver disease.
  • Elderly patients: start with low dose and titrate slowly due to increased sensitivity.
  • Drug hypersensitivity: discontinue if signs of allergic reaction appear.
  • Concomitant antihypertensives: monitor for additive hypotensive effects.
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase plasma levels and risk of hypotension.
  • Other calcium‑channel blockers: additive vasodilatory effect leading to excessive blood pressure drop.
  • Grapefruit juice: inhibits metabolism and raises drug concentration.

Moderate Interactions (Monitor Closely):\n- Diuretics: enhanced antihypertensive effect, monitor electrolytes.

  • Beta‑blockers: combined effect on heart rate and blood pressure, adjust dosing as needed.
  • ACE inhibitors or ARBs: additive blood pressure reduction, watch for symptomatic hypotension.
  • NSAIDs: may diminish antihypertensive efficacy, assess blood pressure control.
  • Antiplatelet agents: increased risk of bleeding, especially if vascular fragility is present.

Frequently Asked Questions

Lercanidipin-Hcl Teva contains lercanidipine hydrochloride, which is prescribed to lower elevated blood pressure in adults with hypertension. By relaxing the smooth muscle of blood vessels, it helps achieve and maintain target blood‑pressure levels, reducing the risk of cardiovascular complications associated with uncontrolled hypertension.

Lercanidipine selectively blocks L‑type calcium channels in the smooth muscle of arteries. This inhibition prevents calcium entry that is required for muscle contraction, causing the vessels to dilate. The resulting reduction in peripheral vascular resistance lowers arterial pressure without significantly affecting heart rate or contractility.

The appropriate dose of Lercanidipin-Hcl Teva is determined by the prescribing healthcare professional based on the patient’s clinical condition, response to therapy, and any co‑existing medical issues. Dosage adjustments are made according to blood‑pressure targets and tolerability, and patients should follow the prescriber’s instructions precisely.

The safety of lercanidipine in pregnancy and lactation has not been established, and the product is classified as pregnancy category unknown. It should only be used if the potential benefit justifies any possible risk to the fetus. Breastfeeding mothers should consult their physician, as the drug may be excreted in breast milk.

To request Lercanidipin-Hcl Teva, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, and will ask for trade or institutional credentials. The sales team then provides pricing, availability, shipping details and assists with any import documentation needed.

Lercanidipine belongs to the dihydropyridine calcium‑channel blocker class, offering potent vasodilation with a relatively long half‑life, which can provide once‑daily dosing. Compared with other classes such as ACE inhibitors or beta‑blockers, it has a lower incidence of cough but may cause more peripheral edema. Choice of therapy depends on individual patient profile, comorbidities and tolerability.

Lercanidipin-Hcl Teva tablets should be stored at room temperature, below 25 °C, in the original packaging. Protect the product from moisture, excessive heat and direct sunlight to maintain stability and potency throughout its shelf life.

The medication is taken orally, usually once daily, with or without food as directed by the prescriber. Swallow the tablet whole with a glass of water and do not crush or chew it. Consistency in the time of day helps maintain stable blood‑pressure control.

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

Lercanidipine is contraindicated in individuals with known hypersensitivity to the drug or any component of the formulation. It should also be avoided in patients with severe hepatic impairment and in those taking strong CYP3A4 inhibitors that could markedly increase drug levels. Clinicians must evaluate each patient’s medical history before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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