Product image of Kaliumlosartanhydrochloorthiazide Eg (Eurogenerics) (Losartan Potassium, Hydrochlorothiazide) supplied by GNH India

Kaliumlosartanhydrochloorthiazide Eg (Eurogenerics)

Active Ingredient:
Losartan Potassium, Hydrochlorothiazide
Origin:
EU

Kaliumlosartanhydrochloorthiazide Eg (Eurogenerics) (Losartan Potassium, Hydrochlorothiazide)

Losartan potassium, the active ingredient in Kaliumlosartanhydrochloorthiazide Eg, is an angiotensin II receptor blocker presented as a combination tablet for oral use. It treats hypertension, often together with hydrochlorothiazide, in adult patients.

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

Manufacturer / TM Owner

Eurogenerics N.V./S.A.

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Indications & Clinical Uses

Kaliumlosartanhydrochloorthiazide Eg acts on the renin‑angiotensin‑aldosterone system and renal sodium handling to lower blood pressure.

  • Hypertension: provides effective blood‑pressure control in adults.
  • Diabetic nephropathy: helps slow progression of kidney damage associated with diabetes.
  • Heart failure with reduced ejection fraction: reduces afterload and improves symptoms when combined with standard therapy.

How It Works

  • Losartan potassium selectively blocks AT1 receptors, preventing angiotensin II‑mediated vasoconstriction, aldosterone release and sodium retention. Hydrochlorothiazide inhibits NaCl reabsorption in the distal convoluted tubule, increasing urinary excretion of sodium and water, thereby reducing plasma volume and further lowering arterial pressure.

Side Effects

Kaliumlosartanhydrochloorthiazide Eg may cause a range of adverse reactions.

Common Side Effects

  • Dizziness: feeling light‑headed, especially after standing.
  • Headache: mild to moderate intensity.
  • Fatigue: general tiredness or lack of energy.
  • Increased urination: due to the diuretic component.
  • Electrolyte imbalance: especially low potassium levels.
  • Mild gastrointestinal upset: nausea or abdominal discomfort.

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips, tongue or throat.
  • Acute kidney injury: sudden decline in renal function.
  • Hyperkalemia: elevated blood potassium concentrations.
  • Severe dehydration: excessive fluid loss.
  • Hepatic injury: abnormal liver enzyme elevations.
  • Blood dyscrasias: rare blood cell abnormalities such as agranulocytosis.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for safety.

  • Monitor electrolytes: check potassium and sodium levels regularly.
  • Assess renal function: evaluate kidney function before and during treatment.
  • Avoid in severe hepatic impairment: use with caution or consider alternatives.
  • Pregnancy: risk category unknown; discuss potential benefits and risks with a healthcare provider.
  • Drug interactions: review concomitant medications for potential interactions.
  • Store at ambient temperature: keep in the original pack, protect from moisture and light.

Avoid Interactions

Kaliumlosartanhydrochloorthiazide Eg can interact with several drug classes.

Major Interactions (Avoid)

  • Potassium‑sparing diuretics: may cause dangerous hyperkalemia.
  • ACE inhibitors or ARBs combined with aliskiren in diabetic patients: increased risk of renal dysfunction.
  • Lithium: concomitant use can raise lithium concentrations.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may blunt antihypertensive effect and affect renal function.
  • CYP2C9 inhibitors (e.g., fluconazole): can increase losartan plasma levels.
  • Additional thiazide diuretics or antihypertensives: additive blood‑pressure lowering may require dose adjustment.

Frequently Asked Questions

Kaliumlosartanhydrochloorthiazide Eg is a prescription combination of losartan potassium and hydrochlorothiazide used to treat hypertension. It lowers blood pressure by blocking angiotensin II receptors and promoting diuresis, helping reduce the risk of cardiovascular complications associated with high blood pressure.

Losartan potassium selectively blocks AT1 receptors, preventing angiotensin II from causing vasoconstriction, aldosterone release, and sodium retention. This results in relaxed blood vessels and reduced fluid volume, which together lower systemic blood pressure.

The dosage of Kaliumlosartanhydrochloorthiazide Eg is determined by the prescribing clinician based on the patient’s blood‑pressure goals, renal function, and overall health status. Patients should follow the exact regimen provided by their healthcare professional.

The safety of Kaliumlosartanhydrochloorthiazide Eg in pregnancy or while breastfeeding has not been definitively established. Physicians should weigh potential benefits against possible risks and consider alternative therapies when treating pregnant or nursing individuals.

To order, 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 any necessary import documentation.

Compared with single‑agent therapies, the losartan‑hydrochlorothiazide combo offers dual mechanisms—RAAS blockade and diuresis—in one tablet, often achieving better blood‑pressure control with fewer pills. It is commonly used when monotherapy does not reach target pressures.

Kaliumlosartanhydrochloorthiazide Eg should be stored at ambient temperature, below 25 °C, in its original container. Keep the product away from moisture, heat and direct sunlight to maintain stability and potency.

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

Serious risks include angioedema (swelling of the face, lips, tongue or throat), severe kidney impairment, hyperkalemia (high potassium levels), and significant dehydration. Patients should seek immediate medical attention if they experience any of these symptoms.

Individuals with known hypersensitivity to losartan, hydrochlorothiazide, or any component of the formulation should avoid this product. It is also contraindicated in patients with severe hepatic impairment, and caution is advised in those with advanced renal disease or electrolyte disturbances.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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