Product image of Naprilene (Enalapril Maleate) supplied by GNH India

Naprilene

Active Ingredient:
Enalapril Maleate
Origin:
EU

Naprilene (Enalapril Maleate)

Enalapril, the active ingredient in Naprilene, is an ACE inhibitor presented as an oral tablet for oral use. It is used to lower elevated blood pressure and to manage heart failure, including after myocardial infarction, in adult patients.
GNH India supplies Naprilene as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Alfasigma S.P.A.

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Indications & Clinical Uses

  • Naprilene, an ACE inhibitor, is employed in several cardiovascular conditions where the renin‑angiotensin system contributes to disease progression.
  • Hypertension: lowers systolic and diastolic pressure, reducing risk of stroke and heart attack.
  • Heart failure: improves symptoms and survival by decreasing afterload.
  • Asymptomatic left ventricular dysfunction: slows progression to overt heart failure.
  • Post‑myocardial infarction: reduces mortality and reinfarction rates.

How It Works

  • Enalapril is converted in vivo to enalaprilat, which binds to the active site of angiotensin‑converting enzyme (ACE). This inhibition prevents the conversion of angiotensin I to the potent vasoconstrictor angiotensin II and reduces aldosterone secretion, leading to vasodilation, decreased peripheral resistance, and lower blood pressure.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Cough: dry, persistent throat irritation.
  • Dizziness or light‑headedness, especially after the first dose.
  • Headache: mild to moderate intensity.
  • Fatigue: general feeling of tiredness.
  • Hypotension: especially in volume‑depleted patients.

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips, tongue, or airway.
  • Hyperkalemia: elevated serum potassium levels.
  • Acute renal impairment: sudden decrease in kidney function.
  • Neutropenia or agranulocytosis: marked reduction in white blood cells.
  • Hepatic dysfunction: abnormal liver enzyme elevations.

Precautions & Warnings

  • Before initiating therapy, clinicians should assess relevant clinical factors and monitor patients during treatment.
  • Monitor blood pressure: check regularly to avoid excessive hypotension.
  • Assess renal function: obtain baseline creatinine and repeat as needed.
  • Check serum potassium: especially when combined with potassium‑sparing agents.
  • Avoid use in pregnancy: contraindicated due to fetal toxicity (Category D).
  • Use caution in aortic stenosis: may precipitate severe hypotension.
  • Store at below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Enalapril may interact with several drug classes, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Aliskiren (in diabetic patients): heightened risk of hypotension and renal dysfunction.
  • Potassium‑sparing diuretics (e.g., spironolactone): may cause dangerous hyperkalemia.
  • High‑dose NSAIDs: can blunt antihypertensive effect and impair renal function.

Moderate Interactions (Monitor Closely)

  • Thiazide diuretics: additive blood‑pressure lowering effect.
  • Lithium: increased lithium concentrations, risk of toxicity.
  • Concurrent ACE inhibitors or ARBs: additive renin‑angiotensin blockade, avoid combined use.

Frequently Asked Questions

Naprilene contains enalapril, an ACE inhibitor indicated for managing hypertension, chronic heart failure, asymptomatic left ventricular dysfunction, and for reducing cardiovascular risk after a myocardial infarction. It works by lowering blood pressure and decreasing the workload on the heart.

Enalapril is converted to enalaprilat, which blocks the angiotensin‑converting enzyme. This prevents formation of angiotensin II, a strong vasoconstrictor, and reduces aldosterone release, leading to vasodilation, lower peripheral resistance, and decreased blood pressure.

The appropriate dose of Naprilene is determined by the prescribing clinician based on the patient’s medical condition, response to therapy, and renal function. Dosage adjustments are individualized and should follow the prescriber’s instructions.

Naprilene is classified as pregnancy Category D, indicating evidence of fetal risk and it is contraindicated in pregnancy. Safety during breastfeeding has not been established, so it should be used only if the potential benefit justifies the potential risk to the infant.

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

Naprilene (enalapril) shares the same class mechanism as other ACE inhibitors such as lisinopril or ramipril. Differences lie mainly in pharmacokinetic profiles, dosing frequency, and individual patient tolerance. Choice among agents is guided by clinical response, side‑effect profile, and physician preference.

Naprilene tablets should be stored at temperatures below 25 °C, in the original container, protected from moisture and direct sunlight. Keeping the product in a dry, cool place helps maintain its stability and potency.

Naprilene is taken orally, usually once or twice daily as directed by a healthcare professional. Tablets should be swallowed whole with a glass of water and can be taken with or without food, unless otherwise advised by the prescriber.

Serious adverse events include angioedema, which can affect the airway, severe hypotension, hyperkalemia, and acute renal impairment. Patients should be instructed to seek immediate medical attention if they experience swelling of the face or throat, sudden dizziness, or a rapid decline in kidney function.

Naprilene is contraindicated in patients with a known hypersensitivity to enalapril or any ACE inhibitor, those with a history of angioedema related to ACE‑inhibitor therapy, and pregnant women. Caution is also advised for individuals with severe renal artery stenosis or significant aortic stenosis.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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