Product image of Olmesartan/Hct Krka (Olmesartan Medoxomil, Hydrochlorothiazide) supplied by GNH India

Olmesartan/Hct Krka

Active Ingredient:
Olmesartan Medoxomil, Hydrochlorothiazide
Origin:
EU

Olmesartan/Hct Krka (Olmesartan Medoxomil, Hydrochlorothiazide)

Olmesartan medoxomil, the active ingredient in Olmesartan/Hct Krka, is an Angiotensin II receptor blocker (ARB) presented as a tablet for oral use. It is combined with hydrochlorothiazide to treat hypertension in adult patients.
GNH India supplies Olmesartan/Hct Krka as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Olmesartan/Hct acts on the renin‑angiotensin‑aldosterone system to lower elevated blood pressure.

  • Hypertension: provides sustained reduction of systolic and diastolic blood pressure in essential hypertension.
  • Hypertension with fluid retention: enhances diuretic effect to control volume overload.
  • High‑risk cardiovascular patients: contributes to risk reduction when combined with lifestyle measures.

How It Works

  • Olmesartan medoxomil selectively blocks the AT1 subtype of angiotensin II receptors, preventing vasoconstriction and aldosterone release. Hydrochlorothiazide inhibits sodium‑chloride reabsorption in the distal convoluted tubule, promoting natriuresis and diuresis. The combined actions reduce peripheral vascular resistance and plasma volume, resulting in lower arterial pressure.

Side Effects

Common Side Effects

  • Dizziness: mild to moderate light‑headedness, especially after the first dose.
  • Headache: transient cephalic discomfort.
  • Fatigue: general tiredness without specific cause.
  • Increased urination: due to the diuretic component.
  • Electrolyte imbalance: mild changes in potassium or sodium levels.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure causing fainting.
  • Acute renal impairment: sudden decrease in kidney function.
  • Hyperkalemia: elevated potassium that may affect cardiac rhythm.
  • Angioedema: swelling of face, lips, tongue, or airway.
  • Life‑threatening electrolyte disturbances: severe hyponatremia or hypokalemia.

Precautions & Warnings

Olmesartan/Hct should be used with careful clinical monitoring.

  • Blood pressure monitoring: check regularly to avoid excessive lowering.
  • Renal function assessment: evaluate serum creatinine before and during therapy.
  • Electrolyte surveillance: monitor sodium and potassium levels, especially with diuretic use.
  • Pregnancy avoidance: contraindicated in the second and third trimesters due to fetal risk.
  • Elderly dose consideration: start with lower dose and titrate cautiously.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Olmesartan/Hct may interact with several medicines that affect blood pressure, renal function, or electrolyte balance.

Major Interactions (Avoid)

  • Aliskiren (in diabetic patients): risk of renal dysfunction and hyperkalemia.
  • Potassium‑sparing diuretics: may cause dangerous hyperkalemia.
  • Lithium: increased lithium levels and toxicity.
  • ACE inhibitors: additive effect on potassium and renal function.
  • NSAIDs: may blunt antihypertensive effect and impair renal function.

Moderate Interactions (Monitor Closely)

  • Other antihypertensives: may require dose adjustment to prevent hypotension.
  • Non‑potassium‑sparing diuretics: monitor electrolytes.
  • Antidiabetic agents: blood glucose may improve, requiring dose changes.
  • CYP450 inhibitors (e.g., azole antifungals): may increase olmesartan levels.
  • Antacids containing aluminum or magnesium: may reduce absorption of olmesartan.

Frequently Asked Questions

Olmesartan/Hct is a fixed‑dose combination of olmesartan medoxomil, an angiotensin II receptor blocker, and hydrochlorothiazide, a thiazide diuretic. It is prescribed to lower elevated blood pressure in adults with essential hypertension, often when additional diuretic therapy is needed to control fluid retention.

Olmesartan medoxomil selectively blocks AT1 receptors for angiotensin II, preventing vasoconstriction and aldosterone release. This leads to relaxation of blood vessels and reduced sodium and water retention, thereby lowering systemic blood pressure.

The specific dose of Olmesartan/Hct is determined by the prescribing clinician based on the patient’s blood pressure, renal function, and response to therapy. Dosage adjustments are made individually; no fixed regimen is provided here.

Olmesartan/Hct is contraindicated in pregnancy, especially during the second and third trimesters, because it can harm the developing fetus. Limited data are available for breastfeeding; the drug may pass into milk, so use is generally discouraged unless clearly needed.

To place an 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.

Olmesartan/Hct combines an ARB with a thiazide diuretic, offering both vasodilation and diuretic effects in a single tablet. Compared with monotherapy ARBs or ACE inhibitors, the combination often achieves better blood‑pressure control with fewer pills, but it may carry a higher risk of electrolyte disturbances.

Olmesartan/Hct tablets should be stored at ambient temperature, below 25 °C, in the original packaging to protect them from moisture and light. Keep the container tightly closed and out of reach of children.

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

Serious risks include severe hypotension, acute kidney injury, hyperkalemia, and angioedema. Patients should be monitored for signs of fainting, rapid weight gain, swelling of the face or throat, and changes in kidney function or electrolyte levels.

Olmesartan/Hct should not be used by individuals with known hypersensitivity to olmesartan, hydrochlorothiazide, or any component of the formulation. It is also contraindicated in pregnant women (second and third trimesters), patients with severe renal impairment, and those with a history of angioedema related to ARB therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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