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

Olmesartan Medoxomil/Hydrochlorothiazide Krka

Active Ingredient:
Olmesartan Medoxomil, Hydrochlorothiazide
Origin:
EU

Olmesartan Medoxomil/Hydrochlorothiazide Krka (Olmesartan Medoxomil, Hydrochlorothiazide)

Olmesartan medoxomil, the active ingredient in Olmesartan Medoxomil/Hydrochlorothiazide Krka, is an Angiotensin II receptor blocker (ARB) presented as an oral tablet for systemic use. It is employed to treat hypertension in adult patients, often in combination with a thiazide diuretic to improve blood‑pressure control.

GNH India supplies Olmesartan Medoxomil/Hydrochlorothiazide Krka as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company emphasizes quality assurance, regulatory compliance and reliable global logistics to ensure product integrity through validated manufacturing processes and continuous monitoring.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

  • Olmesartan medoxomil/hydrochlorothiazide is indicated for the management of hypertension, a common cardiovascular condition.
  • Hypertension: reduces systolic and diastolic blood pressure, helping to lower the risk of cardiovascular events.

How It Works

  • Olmesartan medoxomil selectively blocks the AT1 receptor, preventing angiotensin II from causing vasoconstriction and aldosterone release, which leads to vasodilation and reduced sodium retention. Hydrochlorothiazide acts on the distal convoluted tubule to inhibit NaCl reabsorption, increasing urinary excretion of sodium and water, thereby decreasing plasma volume and contributing to lower blood pressure.

Side Effects

Adverse reactions reported with Olmesartan medoxomil/hydrochlorothiazide span a range of frequencies and severities.

Common Side Effects

  • Dizziness or light‑headedness
  • Headache
  • Fatigue or weakness
  • Increased urination
  • Mild electrolyte disturbances (e.g., low potassium)
  • Gastrointestinal upset such as nausea or abdominal discomfort

Serious or Rare Side Effects

  • Angioedema (swelling of face, lips, tongue)
  • Severe hypotension (excessively low blood pressure)
  • Acute renal impairment or failure
  • Hyperkalemia (elevated potassium levels)
  • Pancreatitis
  • Anaphylactic or severe allergic reactions

Precautions & Warnings

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

  • Blood pressure monitoring: ensure adequate control and avoid excessive lowering.
  • Renal function assessment: check serum creatinine and eGFR, especially in patients with pre‑existing kidney disease.
  • Electrolyte surveillance: monitor potassium and sodium levels during diuretic therapy.
  • Hepatic impairment: use with caution in patients with liver dysfunction.
  • Hypersensitivity: discontinue if signs of allergic reaction appear.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Olmesartan medoxomil/hydrochlorothiazide may interact with several drug classes, influencing efficacy or safety.

Major Interactions (Avoid)

  • Aliskiren (combined use can increase risk of renal impairment and hyperkalemia).
  • Potassium‑sparing diuretics (may cause dangerous hyperkalemia).
  • NSAIDs (can attenuate antihypertensive effect and affect renal function).
  • Lithium (increased lithium toxicity).
  • ACE inhibitors (heightened risk of hyperkalemia and renal dysfunction).

Moderate Interactions (Monitor Closely)

  • Other antihypertensives (additive blood‑pressure lowering effect).
  • Loop or thiazide diuretics (potassium balance may shift).
  • Antidiabetic agents (blood‑glucose control may be altered).
  • CYP450 inhibitors (potentially affect olmesartan metabolism).
  • Oral contraceptives (may raise blood pressure).

Frequently Asked Questions

Olmesartan Medoxomil/Hydrochlorothiazide is a prescription medication used to treat hypertension. It combines an angiotensin II receptor blocker with a thiazide diuretic to lower blood pressure by relaxing blood vessels and reducing fluid volume.

Olmesartan medoxomil blocks the AT1 receptors for angiotensin II, preventing vasoconstriction and aldosterone release, which leads to vessel relaxation and reduced sodium retention. Hydrochlorothiazide increases urine output by inhibiting sodium reabsorption in the distal tubule, further lowering blood pressure.

The specific dose and dosing schedule are determined by the prescribing clinician based on the patient’s medical condition, response to therapy, and other individual factors. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for use during pregnancy or lactation are limited. The medication should only be used if the potential benefit justifies the potential risk to the fetus or infant, and it must be prescribed by a qualified health professional after careful consideration.

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/HCTZ offers a dual mechanism—an ARB plus a thiazide diuretic—providing effective blood‑pressure reduction in patients who need both vasodilation and volume control. Compared with monotherapy agents, the combination can achieve target pressures with fewer pills, but individual response and tolerance vary.

The product should be stored at room temperature, below 25 °C, in its original packaging. It must be kept away from moisture, direct sunlight, and sources of heat to maintain stability and potency throughout its shelf life.

The medication is taken orally, usually once daily, with or without food, as directed by the prescribing physician. Patients should swallow the tablet whole with a glass of water and avoid crushing or chewing unless specifically instructed.

Serious risks include angioedema, severe hypotension, acute kidney injury, and hyperkalemia. Patients should seek immediate medical attention if they experience swelling of the face or throat, dizziness, rapid weight loss, or signs of electrolyte imbalance.

Individuals with known hypersensitivity to olmesartan, hydrochlorothiazide, or any component of the formulation should avoid the drug. It is also contraindicated in patients with severe renal impairment, hyperkalemia, or those taking interacting medications such as aliskiren in combination with an ACE inhibitor or ARB.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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