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

Olmesartan Medoxomil/Hydrochloorthiazide Krka

Active Ingredient:
Olmesartan Medoxomil, Hydrochlorothiazide
Origin:
EU

Olmesartan Medoxomil/Hydrochloorthiazide Krka (Olmesartan Medoxomil, Hydrochlorothiazide)

Olmesartan medoxil, the active ingredient in Olmesartan Medoxomil/Hydrochloorthiazide Krka, is an angiotensin II receptor blocker presented as a tablet for oral use. It is used to manage high blood pressure, often in combination with a diuretic, and is prescribed for adults.

GNH India supplies Olmesartan Medoxomil/Hydrochloorthiazide Krka as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Olmesartan Medoxil/Hydrochlorothiazide is indicated for hypertension management, acting on the renin‑angiotensin‑aldosterone system and fluid balance.

  • Hypertension: lowers systolic and diastolic blood pressure to reduce cardiovascular risk.
  • Hypertension with fluid retention: provides additional blood‑pressure reduction through diuretic action.
  • Hypertension in patients who require an angiotensin receptor blocker combined with a thiazide diuretic: offers convenient dual therapy in a single tablet.

How It Works

  • Olmesartan medoxil selectively blocks the binding of angiotensin II to the AT1 receptor on vascular smooth‑muscle and adrenal cells, preventing vasoconstriction and aldosterone release. Hydrochlorothiazide inhibits sodium‑chloride reabsorption in the distal convoluted tubule, promoting natriuresis and diuresis, which together lower systemic vascular resistance and blood volume.

Side Effects

Adverse reactions may range from mild to severe and should be monitored during therapy.

Common Side Effects

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

Serious or Rare Side Effects

  • Severe hypotension
  • Acute kidney injury
  • Hyperkalemia
  • Angio‑edema
  • Liver function abnormalities
  • Severe skin reactions such as Stevens‑Johnson syndrome

Precautions & Warnings

Before starting therapy, clinicians should assess patient history and monitor relevant parameters.

  • Renal function: evaluate baseline creatinine and eGFR.
  • Electrolytes: check serum potassium and sodium levels.
  • Pregnancy: avoid use; drug is contraindicated in the second and third trimesters.
  • Concomitant NSAIDs: may reduce antihypertensive effect and increase renal risk.
  • Gout: monitor uric acid as thiazides can precipitate attacks.

Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Olmesartan Medoxil/Hydrochlorothiazide may interact with several drug classes; monitoring and dosage adjustments are often required.

Major Interactions (Avoid)

  • Aliskiren: combined use can cause excessive potassium elevation and renal impairment.
  • Potassium‑saving diuretics or supplements: risk of hyper‑kalemia.
  • Lithium: increased lithium levels may lead to toxicity.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may blunt antihypertensive response and affect renal function.
  • ACE inhibitors or other ARBs: additive blood‑pressure lowering effect, risk of hypotension.
  • Antidiabetic drugs: may enhance hypoglycaemic effect.
  • CYP450 inhibitors: may modestly increase olmesartan concentrations.

Frequently Asked Questions

Olmesartan Medoxil/Hydrochlorothiazide is a fixed‑dose combination used to treat primary hypertension, especially in patients who need both an angiotensin‑II receptor blocker and a thiazide‑type diuretic to achieve target blood‑pressure levels.

Olmesartan medoxil blocks the AT1 receptors for angiotensin II, preventing vasoconstriction and aldosterone release, while hydrochlorothiazide reduces sodium and water reabsorption in the kidney, together lowering vascular resistance and circulating volume.

The prescribed dose is determined by the treating physician based on the patient’s blood‑pressure readings, renal function, and overall clinical profile; dosing adjustments are made during follow‑up visits.

The combination is contraindicated in pregnancy, particularly in the second and third trimesters, due to risk of fetal toxicity. Limited data exist for breastfeeding, so it should be used only if the potential benefit outweighs the risk.

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 required import documentation.

Compared with separate tablets of an ARB and a thiazide, this fixed‑dose combo offers convenience and improved adherence. It provides similar blood‑pressure control to other ARB‑thiazide combinations such as losartan‑hydrochlorothiazide, but individual patient response may vary.

Store the tablets at temperatures below 25 °C in the original container, protected from moisture and direct sunlight. Do not expose the product to excessive heat or humidity.

The medication is taken orally, usually once daily, with or without food, as directed by the prescribing clinician.

Serious adverse events include severe hypotension, acute kidney injury, hyper‑kalemia, angio‑edema and rare severe skin reactions. Patients should be monitored for signs of these conditions, especially during treatment initiation.

Patients with known hypersensitivity to olmesartan, hydrochlorothiazide or any excipients, those with severe renal impairment, hyper‑kalemia, or who are pregnant should avoid this combination.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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