Product image of Kaparlon-S (Enalapril Maleate) supplied by GNH India

Kaparlon-S

Active Ingredient:
Enalapril Maleate
Origin:
EU

Kaparlon-S (Enalapril Maleate)

Enalapril Maleate, the active ingredient in Kaparlon‑S, is an ACE inhibitor presented as an oral tablet for oral use. It is indicated for adults with essential hypertension, chronic heart failure, and diabetic nephropathy, and is administered under medical supervision to lower blood pressure and reduce cardiac workload.

GNH India supplies Kaparlon‑S as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with established quality‑assurance processes and regulatory approvals across EU and other markets. Our supply chain ensures timely delivery and compliance with international pharmacopeial standards.

Manufacturer / TM Owner

Anfarm Hellas Sa

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Indications & Clinical Uses

  • Enalapril acts on the renin‑angiotensin‑aldosterone system to lower blood pressure and improve cardiac function.
  • Hypertension: reduces systolic and diastolic pressure, decreasing cardiovascular risk.
  • Heart failure: improves symptoms and lowers hospitalization by decreasing afterload.
  • Diabetic nephropathy: slows renal function decline by lowering intraglomerular pressure.

How It Works

  • Enalapril maleate is a prodrug that is hydrolyzed to enalaprilat, a potent inhibitor of angiotensin‑converting enzyme (ACE). By blocking ACE, it prevents conversion of angiotensin I to the vasoconstrictor angiotensin II, leading to vasodilation, reduced aldosterone secretion, and decreased sodium and water retention. These effects contribute to its therapeutic benefit in cardiovascular and renal disorders.

Side Effects

Enalapril may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Cough: persistent dry cough.
  • Dizziness or light‑headedness, especially after the first dose.
  • Headache.
  • Fatigue.
  • Mild hyperkalemia.

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips, tongue, or airway.
  • Severe hypotension: marked drop in blood pressure.
  • Acute renal failure: sudden decline in kidney function.
  • Neutropenia or agranulocytosis: rare blood disorder.

Precautions & Warnings

Before initiating enalapril therapy, several safety considerations should be reviewed.

  • Blood pressure monitoring: check baseline and periodic readings to avoid excessive hypotension.
  • Renal function assessment: evaluate serum creatinine and eGFR before and during treatment.
  • Electrolyte surveillance: monitor potassium levels, especially when combined with potassium‑sparing agents.
  • History of angioedema: avoid use in patients with prior ACE‑inhibitor‑induced angioedema.
  • Pregnancy and lactation: use only if clearly needed, after risk‑benefit evaluation.
  • Store at room temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Enalapril can interact with several medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Aliskiren in diabetic patients: combined use may increase risk of renal impairment, hyperkalemia, and hypotension.
  • Lithium: enalapril may increase lithium levels, risking toxicity.
  • Potassium‑sparing diuretics (e.g., spironolactone): may cause significant hyperkalemia.

Moderate Interactions (Monitor Closely)

  • NSAIDs (e.g., ibuprofen): may reduce antihypertensive effect and impair renal function.
  • Thiazide diuretics: may enhance hypotensive response, requiring dose adjustment.
  • Antidiabetic drugs (insulin, sulfonylureas): may need monitoring of blood glucose as enalapril can improve glycemic control.

Frequently Asked Questions

Kaparlon‑S contains enalapril maleate, an ACE inhibitor prescribed to treat high blood pressure, manage chronic heart failure, and slow the progression of diabetic kidney disease. It works by relaxing blood vessels, which helps lower systemic pressure and reduces the workload on the heart.

Enalapril is converted in the body to enalaprilat, which blocks the angiotensin‑converting enzyme. This inhibition prevents the formation of angiotensin II, a potent vasoconstrictor, leading to vessel relaxation, reduced aldosterone release, and lower blood pressure.

The appropriate dose of Kaparlon‑S is individualized by a qualified healthcare professional based on the patient’s medical condition, blood‑pressure response, renal function, and other concurrent medications. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for enalapril in pregnancy are limited, and the drug is generally avoided unless the potential benefit outweighs the risk. It is also excreted in breast milk, so breastfeeding mothers should consult their physician before using Kaparlon‑S.

To place an order, submit an enquiry on the Kaparlon‑S 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.

Kaparlon‑S is pharmacologically equivalent to other enalapril products and shares the same efficacy and safety profile as other ACE inhibitors such as lisinopril or ramipril. Compared with angiotensin‑II receptor blockers, ACE inhibitors also reduce bradykinin breakdown, which can lead to a characteristic dry cough.

Store Kaparlon‑S at room temperature, below 25 °C, in its original packaging. Keep the container tightly closed, protect it from moisture, heat and direct sunlight, and keep it out of reach of children.

Kaparlon‑S is taken orally, usually once or twice daily as directed by the prescriber. It should be swallowed whole with a glass of water, and can be taken with or without food. Patients should not crush or chew the tablet unless specifically instructed.

The most serious adverse events include angioedema (swelling of the face, lips, tongue, or airway), severe hypotension, acute kidney injury, and significant hyperkalemia. Patients should seek immediate medical attention if they experience swelling, difficulty breathing, sudden dizziness, or a rapid decline in urine output.

Kaparlon‑S should be avoided in individuals with a known hypersensitivity to enalapril or any ACE inhibitor, a history of angioedema related to ACE‑inhibitor therapy, and in patients with severe renal artery stenosis. Caution is also advised for those with advanced kidney disease or high potassium levels.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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