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

Lercapress

Active Ingredient:
Enalapril Maleate, Lercanidipine Hydrochloride
Origin:
EU

Lercapress (Enalapril Maleate, Lercanidipine Hydrochloride)

Enalapril maleate and lercanidipine hydrochloride, the active ingredients in Lercapress, are an ACE inhibitor and a calcium‑channel blocker presented as an oral tablet for systemic use. They work together to lower blood pressure in adults with hypertension.
GNH India supplies Lercapress 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

Lercapress is an antihypertensive combination that acts on the renin‑angiotensin system and vascular smooth‑muscle calcium channels.

  • Essential hypertension: lowers systolic and diastolic pressure in patients with primary hypertension.
  • Isolated systolic hypertension: helps control elevated systolic pressure, especially in older adults.
  • Secondary hypertension: may be incorporated into therapy when high blood pressure results from another underlying condition.

How It Works

  • Enalapril maleate inhibits angiotensin‑converting enzyme, reducing formation of angiotensin II and decreasing vasoconstriction. Lercanidipine hydrochloride blocks L‑type calcium channels in arterial smooth muscle, producing vasodilation. The complementary actions result in additive reduction of systemic vascular resistance and blood pressure.

Side Effects

Common Side Effects

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

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips, tongue, or airway.
  • Severe hypotension: markedly low blood pressure causing fainting.
  • Hepatic dysfunction: abnormal liver enzymes or jaundice.
  • Acute renal impairment: sudden decrease in kidney function.
  • Myocardial infarction: chest pain indicative of heart attack.
  • Cardiac arrhythmias: irregular heart rhythms.

Precautions & Warnings

Before initiating therapy, consider the following precautions:

  • Renal impairment: monitor kidney function and adjust therapy as needed.
  • Hepatic impairment: use with caution and observe liver enzymes.
  • Pregnancy: contraindicated; avoid use during pregnancy.
  • Elderly patients: start at lower dose and titrate slowly.
  • Concomitant potassium‑sparing diuretics or supplements: monitor serum potassium levels.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Lercapress can interact with several medicines.

Major Interactions (Avoid)

  • ACE inhibitor with aliskiren in diabetic patients: risk of severe hypotension and renal dysfunction.
  • Lercanidipine with strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may cause excessive blood‑pressure lowering.
  • Concurrent use with other potent antihypertensives: can lead to profound hypotension.
  • Potassium‑containing supplements or salts: increase risk of hyperkalaemia.

Moderate Interactions (Monitor Closely)

  • NSAIDs (ibuprofen, naproxen): may blunt antihypertensive effect.
  • Loop or thiazide diuretics: can amplify electrolyte disturbances.
  • Lithium: enalapril may raise lithium levels, requiring serum monitoring.

Frequently Asked Questions

Lercapress is prescribed to treat hypertension. It combines an ACE inhibitor (enalapril) with a calcium‑channel blocker (lercanidipine) to provide a dual mechanism that lowers both systolic and diastolic blood pressure in adult patients.

Enalapril maleate blocks the angiotensin‑converting enzyme, which reduces the production of angiotensin II, a potent vasoconstrictor. This leads to relaxation of blood vessels, decreased peripheral resistance, and ultimately lower blood pressure.

The appropriate dose of Lercapress is determined by the prescribing healthcare professional based on the patient’s clinical condition, response to therapy, and any concomitant medications. Dosage adjustments are made individually.

Lercapress is generally contraindicated in pregnancy because ACE inhibitors can harm the developing fetus. Safety during breastfeeding has not been established, so the product should be used only if the potential benefit justifies the potential risk.

To place an order, submit an enquiry on the Lercapress 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.

Compared with single‑agent therapies, Lercapress offers a fixed‑dose combination that targets two complementary pathways, often achieving better blood‑pressure control with fewer tablets. It may be preferred over separate ACE inhibitor and calcium‑channel blocker prescriptions for convenience and adherence.

Lercapress tablets should be stored at ambient temperature, below 25 °C, in the original packaging. Keep them away from moisture, heat, and direct sunlight to maintain product stability.

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

The most serious risks include angioedema, severe hypotension, acute renal impairment, and hepatic dysfunction. Patients should seek immediate medical attention if they experience swelling of the face or throat, fainting, sudden loss of kidney function, or signs of liver injury.

Lercapress should be avoided in patients with a known hypersensitivity to enalapril, lercanidipine, or any component of the formulation, as well as in those with a history of angioedema related to ACE inhibitors, severe renal or hepatic impairment, and during pregnancy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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