Product image of Karvezide (Hydrochlorothiazide, Irbesartan) supplied by GNH India

Karvezide

Active Ingredient:
Hydrochlorothiazide, Irbesartan
Origin:
EU

Karvezide (Hydrochlorothiazide, Irbesartan)

Irbesartan, the active ingredient in Karvezide, is an Angiotensin II receptor blocker (ARB) presented as an Irbesartan 150 mg / Hydrochlorothiazide 12.5 mg tablet for oral use. It is indicated for the treatment of hypertension in adult patients, often in combination with lifestyle measures.

GNH India supplies Karvezide as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory‑approved batches for global distribution, ensuring consistent potency and safety across markets.

Manufacturer / TM Owner

Sanofi Winthrop Industrie

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Indications & Clinical Uses

Karvezide combines an ARB and a thiazide diuretic to manage high blood pressure.

  • Essential hypertension: lowers systolic and diastolic blood pressure, reducing cardiovascular risk.
  • Primary hypertension requiring combination therapy: provides additive blood‑pressure control when monotherapy is insufficient.
  • Hypertension with fluid retention: adds diuretic effect to improve volume management.

How It Works

  • Irbesartan selectively blocks the angiotensin II type 1 (AT1) receptor, preventing vasoconstriction and aldosterone release. Hydrochlorothiazide inhibits sodium‑chloride reabsorption in the distal convoluted tubule, promoting diuresis and decreasing plasma volume. The combined actions result in reduced peripheral resistance and lower blood pressure.

Side Effects

Karvezide may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Dizziness or light‑headedness
  • Headache
  • Increased urination or nocturia
  • Fatigue or weakness
  • Electrolyte disturbances (e.g., low potassium)

Serious or Rare Side Effects

  • Severe allergic reaction (rash, swelling, anaphylaxis)
  • Acute kidney injury or worsening renal function
  • Significant hypotension (very low blood pressure)
  • Pancreatitis (rare)
  • Hyperkalemia when combined with potassium‑sparing agents

Precautions & Warnings

Before initiating therapy, certain precautions should be observed.

  • Blood pressure monitoring: ensure adequate control and avoid excessive drops.
  • Renal function assessment: check serum creatinine and eGFR periodically.
  • Electrolyte surveillance: monitor potassium and sodium levels, especially in patients on other diuretics.
  • Pregnancy: contraindicated in pregnancy (Category D) due to fetal risk.
  • Elderly patients: start at lower doses and monitor for orthostatic hypotension.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Karvezide can interact with several drug classes, requiring clinical attention.

Major Interactions (Avoid)

  • Potassium‑sparing diuretics or supplements: risk of hyperkalemia.
  • Lithium: increased lithium levels leading to toxicity.
  • ACE inhibitors or other ARBs: additive renal effects and hyperkalemia.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may reduce antihypertensive efficacy and affect renal function.
  • Antidiabetic agents: diuretic‑induced hypokalemia can alter glucose control.
  • CYP2C9 inhibitors (e.g., fluconazole): may increase irbesartan plasma concentrations.

Frequently Asked Questions

Karvezide is prescribed to lower high blood pressure in adult patients. It combines irbesartan, an angiotensin II receptor blocker, with hydrochlorothiazide, a thiazide diuretic, to provide complementary blood‑pressure reduction.

Irbesartan blocks the AT1 receptors for angiotensin II, preventing vasoconstriction and aldosterone‑mediated sodium retention. This leads to relaxed blood vessels and reduced blood pressure, complementing the diuretic action of hydrochlorothiazide.

The dose of Karvezide is individualized by the prescribing clinician based on the patient’s blood‑pressure profile, renal function, and concomitant medications. The prescriber determines the appropriate strength and dosing schedule.

Karvezide is classified as pregnancy Category D because irbesartan can cause fetal harm. It should not be used during pregnancy. Limited data are available for breastfeeding; the benefits and risks should be evaluated by a healthcare professional.

To order Karvezide, submit an enquiry on the 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 necessary import documentation.

Karvezide offers a fixed‑dose combination of an ARB and a thiazide diuretic, which can simplify therapy compared with taking two separate pills. It provides additive blood‑pressure lowering effects and may improve adherence versus monotherapy, while sharing a similar safety profile to its individual components.

Karvezide 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 potency throughout the shelf life.

Karvezide is taken orally, usually once daily, with or without food, as directed by the prescribing clinician. Swallow the tablet whole with a glass of water; do not crush or chew it.

Serious risks include severe allergic reactions, acute kidney injury, marked hypotension, and hyperkalemia when combined with potassium‑sparing agents. Patients should be monitored for signs of these conditions and seek immediate medical attention if they occur.

Karvezide should be avoided in patients with known hypersensitivity to irbesartan or hydrochlorothiazide, pregnant women, and individuals with severe renal impairment or hyperkalemia. Clinicians should also exercise caution in the elderly and those on interacting medications.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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