Product image of Olmesartán/Hidroclorotiazida Aurovitas (Olmesartan Medoxomil, Hydrochlorothiazide) supplied by GNH India

Olmesartán/Hidroclorotiazida Aurovitas

Active Ingredient:
Olmesartan Medoxomil, Hydrochlorothiazide
Origin:
EU

Olmesartán/Hidroclorotiazida Aurovitas (Olmesartan Medoxomil, Hydrochlorothiazide)

Olmesartan medoxil, the active ingredient in Olmesartán/Hidroclorotiazida Aurovitas, is an angiotensin II receptor blocker (ARB) presented as a oral tablet for systemic use. It treats hypertension, often in combination with a diuretic, and is indicated for adults.

GNH India supplies Olmesartán/Hidroclorotiazida Aurovitas as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Aurovitas Spain,s.A.U.

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Indications & Clinical Uses

Olmesartan/hydrochlorothiazide is used in the management of cardiovascular conditions that involve fluid retention and elevated vascular resistance.

  • Hypertension: low‑blood pressure control in patients requiring combined ARB and diuretic therapy.
  • Congestive heart failure: adjunctive treatment to reduce preload and afterload.
  • Edema associated with renal or hepatic disease: promotes diuresis and lowers blood pressure.
  • Diabetic nephropathy: helps protect renal function by controlling hypertension.

How It Works

  • Olmesartan medoxil is hydrolysed to olmesartan, which selectively blocks the binding of angiotensin II to the AT‑1 receptor on vascular smooth‑muscle and adrenal cells, preventing vasoconstriction and aldosterone release. Hydrochlorothiazide acts on the distal convoluted tubule, inhibiting Na⁺/Cl⁻ reabsorption, increasing urinary sodium and water excretion, and thereby lowering plasma volume and blood pressure.

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
  • Increased urination
  • Electrolyte disturbances (e.g., low potassium)
  • Mild gastrointestinal discomfort

Serious or Rare Side Effects

  • Severe hypotension
  • Acute kidney injury
  • Hyperkalemia or severe electrolyte imbalance
  • Angio‑edema
  • Liver function abnormalities
  • Blood dyscrasias such as agranulocytosis

Precautions & Warnings

Patients should be evaluated for potential risks before initiating therapy and monitored regularly.

  • Renal impairment: adjust dose and monitor kidney function.
  • Hepatic disease: use with caution, monitor liver enzymes.
  • Electrolyte balance: check serum potassium and sodium regularly.
  • Pregnancy: contraindicated in the second and third trimesters; avoid unless clearly needed.
  • Elderly patients: start at lower dose and monitor for orthostatic hypotension.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Olmesartan/hydrochlorothiazide may interact with several drug classes, requiring clinical awareness.

Major Interactions (Avoid)

  • Potassium‑rich supplements or potassium‑sparing diuretics: risk of hyperkalemia.
  • Aliskiren (in diabetic patients): increased risk of renal dysfunction.
  • NSAIDs (high‑dose or chronic use): may blunt antihypertensive effect and impair renal function.

Moderate Interactions (Monitor Closely)

  • Lithium: may increase serum lithium levels.
  • Antidiabetic agents: enhanced hypoglycaemic effect.
  • ACE inhibitors or other ARBs: additive risk of hypotension and renal impairment.
  • Antacids containing aluminium or magnesium: may reduce absorption of olmesartan.

Frequently Asked Questions

Olmesartán/Hidroclorotiazida Aurovitas combines an angiotensin II receptor blocker with a thiazide diuretic and is prescribed to lower high blood pressure, manage fluid retention, and reduce cardiovascular risk in adult patients who need combined therapy.

Olmesartan medoxil is converted to olmesartan, which blocks AT‑1 receptors, preventing angiotensin II‑mediated vasoconstriction and aldosterone release. Hydrochlorothiazide inhibits sodium‑chloride reabsorption in the distal tubule, promoting diuresis and further lowering blood pressure.

The prescribed dose is individualized by a healthcare professional based on the patient’s blood pressure, renal function, and response to therapy. Dosage adjustments follow clinical guidelines and the prescriber’s judgment.

The combination is contraindicated in the second and third trimesters of pregnancy because of potential harm to the fetus. It should be used only if clearly needed in early pregnancy, and breastfeeding mothers should consult a physician before use.

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 ARBs or diuretics, the fixed‑dose combination offers convenience and synergistic blood‑pressure reduction, often achieving target levels with fewer pills. It may be preferred over separate tablets when both mechanisms are indicated.

Store the tablets at temperatures below 25 °C in their original container, protecting them from moisture, heat and direct sunlight. Do not use if the packaging is damaged or the tablets appear discoloured.

The medication 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 unless specifically instructed.

Serious adverse events can include severe hypotension, acute kidney injury, electrolyte disturbances such as hyperkalemia, angio‑edema, and rare blood disorders. Patients should seek immediate medical attention if they experience swelling, difficulty breathing, or sudden loss of kidney function.

Individuals with known hypersensitivity to olmesartan, hydrochlorothiazide, or any tablet excipients, as well as those with severe renal or hepatic impairment, should avoid this medication. It is also contraindicated in later stages of pregnancy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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