Product image of Karvofil (Irbesartan) supplied by GNH India

Karvofil

Active Ingredient:
Irbesartan
Origin:
EU

Karvofil (Irbesartan)

Irbesartan, the active ingredient in Karvofil, is a angiotensin II receptor blocker (ARB) presented as an oral tablet for oral use. It helps lower blood pressure and protects kidney function in certain patients, including those with diabetes.

GNH India supplies Karvofil as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Vocate Φαρμακευτικη Αε

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Indications & Clinical Uses

Irbesartan acts on the renin‑angiotensin system to manage several cardiovascular and renal conditions.

  • Hypertension: reduces systolic and diastolic blood pressure, lowering cardiovascular risk.
  • Diabetic nephropathy: slows progression of kidney damage in patients with type 2 diabetes.
  • Heart failure: improves symptoms and may reduce hospitalization when used as part of standard therapy.

How It Works

  • Irbesartan selectively blocks angiotensin II type 1 (AT1) receptors on vascular smooth muscle and adrenal tissue. By preventing angiotensin II binding, it inhibits vasoconstriction and aldosterone release, leading to vasodilation, reduced sodium‑water retention, and lower blood pressure, while also providing renal protective effects.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Dizziness: feeling light‑headed, especially after standing.
  • Headache: mild to moderate intensity.
  • Fatigue: general tiredness or lack of energy.
  • Nasal congestion: blocked or runny nose.
  • Back pain: discomfort in the lower back region.
  • Upper respiratory infection: symptoms of a cold or mild flu.

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips, tongue, or throat requiring emergency care.
  • Hyperkalemia: elevated blood potassium that can affect heart rhythm.
  • Acute renal failure: sudden loss of kidney function.
  • Hepatic injury: abnormal liver enzymes or jaundice.
  • Severe hypotension: dangerously low blood pressure.
  • Neutropenia: low white‑blood‑cell count increasing infection risk.

Precautions & Warnings

Before initiating therapy, certain safety considerations are recommended.

  • Monitor blood pressure: ensure target levels are achieved without excessive drop.
  • Assess renal function: check serum creatinine and eGFR periodically.
  • Check serum potassium: avoid hyperkalemia, especially with potassium‑sparing agents.
  • Pregnancy caution: use only if benefits outweigh risks (Category D).
  • Contraindicated in bilateral renal artery stenosis: avoid to prevent renal ischemia.
  • Adjust in hepatic impairment: consider lower dose if liver disease is present.
  • Store at room temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Irbesartan may interact with several drug classes, influencing safety or efficacy.

Major Interactions (Avoid)

  • Aliskiren (in diabetes): combined use can increase renal dysfunction risk.
  • Potassium‑sparing diuretics or supplements: may cause dangerous hyperkalemia.
  • ACE inhibitors: concurrent use raises risk of renal impairment and hyperkalemia.
  • NSAIDs: can reduce renal perfusion and worsen kidney function.
  • Lithium: may increase lithium serum concentrations, leading to toxicity.

Moderate Interactions (Monitor Closely)

  • Loop or thiazide diuretics: may enhance antihypertensive effect, requiring BP monitoring.
  • CYP2C9 inhibitors (e.g., fluconazole): can raise irbesartan levels.
  • Other antihypertensives: additive blood‑pressure lowering effect.
  • Rifampin: may lower irbesartan exposure, reducing efficacy.
  • Digoxin: monitor for signs of digoxin toxicity when combined with diuretics.

Frequently Asked Questions

Karvofil contains irbesartan, which is prescribed to lower high blood pressure, to slow kidney damage in patients with type 2 diabetes (diabetic nephropathy), and to improve symptoms in certain cases of heart failure when used as part of standard therapy.

Irbesartan blocks the angiotensin II type 1 receptors on blood vessels and adrenal glands. This prevents angiotensin II‑induced vasoconstriction and aldosterone release, leading to relaxed blood vessels, reduced sodium and water retention, and ultimately lower blood pressure and renal protection.

The appropriate dose of Karvofil is determined by the prescribing clinician based on the individual’s blood‑pressure goals, kidney function, and overall health status. Patients should follow the exact regimen provided by their healthcare professional.

Karvofil is classified as Pregnancy Category D, indicating evidence of risk to the fetus. It should only be used during pregnancy if the potential benefit justifies the risk. Limited data are available for breastfeeding; a decision should be made by the prescriber after weighing benefits and risks.

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

Karvofil (irbesartan) belongs to the ARB class, offering blood‑pressure control similar to ACE inhibitors but with a lower incidence of cough. Compared with other ARBs, its efficacy and safety profile are comparable, while its renal‑protective benefits are especially noted in diabetic patients.

Store Karvofil at room temperature, below 25 °C. Keep the tablets in the original packaging, protect them from moisture and direct sunlight, and ensure the container is tightly closed to maintain product stability.

Karvofil is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with a glass of water. Patients should not split, crush, or chew the tablet unless specifically instructed by a healthcare professional.

Serious risks include angioedema (swelling of the face, lips, tongue, or throat), severe hyperkalemia (high potassium levels), acute renal failure, and marked hypotension. Patients should seek immediate medical attention if they experience swelling, rapid heartbeat, severe dizziness, or sudden loss of kidney function.

Karvofil should be avoided in individuals with known hypersensitivity to irbesartan or any ARB, in patients with bilateral renal artery stenosis, and in those who are pregnant unless the benefit outweighs the risk. Clinicians should also exercise caution in patients with severe liver disease or uncontrolled hyperkalemia.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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