Product image of Lercaprel (Enalapril Maleate, Lercanidipine Hydrochloride) supplied by GNH India

Lercaprel

Active Ingredient:
Enalapril Maleate, Lercanidipine Hydrochloride
Origin:
EU

Lercaprel (Enalapril Maleate, Lercanidipine Hydrochloride)

Enalapril maleate and lercanidipine hydrochloride, the active ingredients in Lercaprel, are an ACE inhibitor and a calcium‑channel blocker presented as an oral tablet for systemic use. The combination is indicated for the treatment of essential hypertension in adult patients.
GNH India supplies Lercaprel as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Recordati Ireland Ltd.

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Indications & Clinical Uses

  • Lercaprel combines an ACE inhibitor and a calcium‑channel blocker to manage high blood pressure.
  • Essential hypertension: provides additive blood‑pressure reduction, helping patients achieve target blood‑pressure goals.

How It Works

  • Enalapril maleate blocks the angiotensin‑converting enzyme, decreasing formation of angiotensin II and reducing aldosterone secretion, which leads to vasodilation. Lercanidipine hydrochloride inhibits L‑type calcium channels in vascular smooth muscle, causing arterial relaxation. The dual action produces an additive effect on lowering systemic vascular resistance and arterial pressure.

Side Effects

Lercaprel may cause a range of adverse reactions, some of which are more frequent than others.

Common Side Effects

  • Cough: dry, persistent throat irritation.
  • Dizziness or light‑headedness, especially after standing.
  • Headache: mild to moderate intensity.
  • Peripheral edema: swelling of the ankles or feet.
  • Flushing: transient warmth and redness of the skin.
  • Fatigue: general feeling of tiredness.

Serious or Rare Side Effects

  • Angioedema: rapid swelling of face, lips, tongue or airway.
  • Severe hypotension: marked drop in blood pressure causing fainting.
  • Hepatic dysfunction: abnormal liver enzyme elevations.
  • Myocardial infarction: rare occurrence of heart attack.
  • Arrhythmias: irregular heart rhythms.
  • Neutropenia: significant reduction in white blood cells.

Precautions & Warnings

Before initiating Lercaprel, several safety considerations should be observed.

  • Renal function monitoring: assess serum creatinine and eGFR periodically.
  • Electrolyte balance: check potassium and sodium levels, especially if using diuretics.
  • History of angioedema: avoid in patients with prior ACE‑inhibitor‑related swelling.
  • Pregnancy: use only if potential benefit justifies risk; data are limited.
  • Concomitant potassium‑sparing agents: evaluate risk of hyperkalaemia.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Lercaprel can interact with several medicines; the significance varies.

Major Interactions (Avoid)

  • Aliskiren in diabetic patients: combined renin‑angiotensin blockade may increase renal risk.
  • Concurrent use of another ACE inhibitor or ARB: may cause excessive hypotension and renal impairment.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): increase lercanidipine plasma levels.
  • Potassium supplements or potassium‑sparing diuretics: risk of hyperkalaemia.
  • Neprilysin inhibitors (e.g., sacubitril): may amplify angioedema risk.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may blunt antihypertensive effect and affect renal function.
  • Thiazide or loop diuretics: may enhance hypotensive response.
  • Other antihypertensives: dose adjustments may be needed to avoid excessive blood‑pressure drop.
  • Grapefruit juice: can modestly raise lercanidipine concentrations.
  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce lercanidipine efficacy.

Frequently Asked Questions

Lercaprel is prescribed to lower elevated blood pressure in adults with essential hypertension. It combines two mechanisms—ACE inhibition and calcium‑channel blockade—to achieve a more pronounced and consistent reduction in systemic vascular resistance, helping patients reach recommended blood‑pressure targets.

Enalapril maleate is an angiotensin‑converting enzyme (ACE) inhibitor. By blocking ACE, it prevents the conversion of angiotensin I to the potent vasoconstrictor angiotensin II, leading to vasodilation, reduced aldosterone secretion, and ultimately lower blood pressure.

The appropriate dose of Lercaprel is determined by the prescribing clinician based on the individual’s blood‑pressure profile, renal function, and concomitant medications. Patients should follow the specific dosing instructions provided by their healthcare professional.

Safety data for Lercaprel in pregnancy and lactation are limited. ACE inhibitors are generally avoided during the second and third trimesters because of fetal toxicity risk. Breastfeeding mothers should consult their physician, as the drug may be excreted in milk.

To request Lercaprel, visit the product page on gnhindia.com, enter the desired quantity, and submit the enquiry form. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.

Compared with single‑agent therapy, Lercaprel offers the advantage of two complementary mechanisms in one tablet, often achieving better blood‑pressure control with fewer pills. It may be preferred over separate ACE inhibitor and calcium‑channel blocker prescriptions for improved adherence, though individual response and tolerability vary.

Lercaprel tablets should be stored at ambient temperature, below 25 °C, in their original packaging. Keep the container tightly closed, protect from moisture and direct sunlight, and keep out of reach of children.

Lercaprel is taken orally, usually once daily, with or without food, as directed by the prescribing clinician. Swallow the tablet whole with a glass of water; do not crush or chew unless specifically instructed.

The most serious adverse reactions include angioedema, severe hypotension, and significant renal impairment. Patients should seek immediate medical attention if they experience swelling of the face or throat, sudden dizziness, or a rapid decline in kidney function.

Lercaprel is contraindicated in individuals with a known hypersensitivity to enalapril, lercanidipine, or any component of the formulation, as well as in patients with a history of angioedema related to ACE‑inhibitor therapy. Caution is also advised for patients with severe renal artery stenosis.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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