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

Lercaril

Active Ingredient:
Enalapril Maleate, Lercanidipine Hydrochloride
Origin:
EU

Lercaril (Enalapril Maleate, Lercanidipine Hydrochloride)

Enalapril maleate / lercanidipine hydrochloride, the active ingredient in Lercaril, is an ACE inhibitor/calcium channel blocker combination presented as a tablet for oral use. It treats essential hypertension in adult patients.

GNH India supplies Lercaril 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

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

  • Essential hypertension: provides additive blood‑pressure reduction when monotherapy is insufficient.
  • Hypertension requiring dual therapy: offers simultaneous ACE inhibition and calcium‑channel blockade in a single tablet.
  • Uncontrolled blood pressure on single agents: improves control by targeting two complementary pathways.

How It Works

  • Enalapril maleate inhibits angiotensin‑converting enzyme, decreasing formation of angiotensin II and reducing vasoconstriction and aldosterone release. Lercanidipine hydrochloride blocks L‑type calcium channels in vascular smooth muscle, leading to arterial vasodilation. The combined actions lower systemic vascular resistance and cardiac afterload, producing an additive antihypertensive effect.

Side Effects

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

Common Side Effects

  • Cough: dry, persistent throat irritation.
  • Dizziness or light‑headedness, especially after standing.
  • Headache: mild to moderate intensity.
  • Peripheral edema: swelling of ankles or feet.
  • Flushing: transient warmth and redness of the skin.
  • Fatigue: generalized 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 enzymes or jaundice.
  • Neutropenia or leukopenia: reduced white‑blood‑cell counts.
  • Myocardial infarction: rare occurrence of heart attack.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

Before prescribing Lercaril, clinicians should evaluate patient‑specific risk factors and monitor therapy.

  • Renal function: assess creatinine clearance and adjust if impaired.
  • Electrolytes: monitor potassium and sodium levels regularly.
  • History of angioedema: avoid use in patients with prior episodes.
  • Pregnancy: contraindicated due to ACE‑inhibitor teratogenicity; discontinue if pregnancy is detected.
  • Elderly patients: start at lower dose and monitor for hypotension.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Lercaril can interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Aliskiren: combined use may cause excessive hypotension and renal impairment.
  • Potassium‑sparing diuretics or supplements: increase risk of hyperkalaemia.
  • Lithium: may raise lithium concentrations, leading to toxicity.
  • Dual ACE‑inhibitor/ARB therapy: heightened risk of renal dysfunction and hyperkalaemia.
  • NSAIDs (high‑dose): can blunt antihypertensive effect and impair renal function.

Moderate Interactions (Monitor Closely)

  • Thiazide diuretics: may enhance antihypertensive effect, watch for volume depletion.
  • CYP3A4 inhibitors (e.g., erythromycin, clarithromycin): can increase lercanidipine levels.
  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce lercanidipine exposure.
  • Other antihypertensives: additive blood‑pressure lowering, monitor for hypotension.
  • Grapefruit juice: may raise lercanidipine concentrations, advise avoidance.

Frequently Asked Questions

Lercaril is a prescription antihypertensive medication that combines enalapril, an ACE inhibitor, with lercanidipine, a calcium‑channel blocker. It is indicated for the treatment of essential hypertension in adult patients, especially when blood‑pressure control requires dual‑mechanism therapy.

Enalapril blocks the angiotensin‑converting enzyme, reducing angiotensin II production and lowering vascular resistance. Lercanidipine blocks L‑type calcium channels in arterial smooth muscle, causing vasodilation. Together they provide additive reduction of systemic blood pressure.

The appropriate dose of Lercaril is determined by the prescribing clinician based on the patient’s blood‑pressure profile, renal function, and response to therapy. Dosage adjustments are made according to clinical judgment and local prescribing guidelines.

Lercaril contains an ACE inhibitor, which is contraindicated in pregnancy because of potential fetal toxicity. It should be discontinued as soon as pregnancy is confirmed. Safety during breastfeeding has not been established, and the drug is generally avoided.

To place an order, submit an enquiry on the Lercaril 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 therapy, Lercaril offers the convenience of two complementary mechanisms in one tablet, potentially improving adherence and blood‑pressure control. It may be preferred over separate ACE‑inhibitor and calcium‑channel blocker prescriptions when dual therapy is indicated.

Store Lercaril at room temperature, below 25 °C, in the original packaging. Keep the product away from moisture, heat and direct sunlight to maintain tablet integrity.

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

Serious risks include angioedema, severe hypotension, hyperkalaemia, and rare hepatic or hematologic abnormalities. Patients should be educated to seek immediate medical attention if they experience swelling of the face or throat, sudden dizziness, or unexplained fatigue.

Lercaril should be avoided in patients with a known history of angioedema related to ACE‑inhibitor therapy, severe renal impairment, hyperkalaemia, or in women who are pregnant. It is also contraindicated when used together with another ACE inhibitor, ARB, or aliskiren in diabetic patients.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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