Product image of Olmesartan Medoxomil E Idroclorotiazide Alter (Olmesartan Medoxomil, Hydrochlorothiazide) supplied by GNH India

Olmesartan Medoxomil E Idroclorotiazide Alter

Active Ingredient:
Olmesartan Medoxomil, Hydrochlorothiazide
Origin:
EU

Olmesartan Medoxomil E Idroclorotiazide Alter (Olmesartan Medoxomil, Hydrochlorothiazide)

Olmesartan medoxomil, the active ingredient in Olmesartan Medoxomil E Idroclorotiazide Alter, is an angiotensin II receptor blocker (ARB) presented as a oral tablet for systemic use. It treats hypertension, often in combination with a thiazide diuretic, and is prescribed for adults requiring blood pressure control.

GNH India supplies Olmesartan Medoxomil E Idroclorotiazide Alter as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Laboratori Alter S.R.L.

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Indications & Clinical Uses

Olmesartan medoxomil/hydrochlorothiazide is indicated for conditions affecting the cardiovascular system, primarily hypertension. It helps lower elevated blood pressure and reduce associated cardiovascular risk.

  • Hypertension: Lowers systolic and diastolic blood pressure, helping to prevent stroke and heart attack.
  • Hypertension with fluid retention: Combines ARB‑mediated vasodilation with diuretic‑induced fluid loss to improve blood pressure control.
  • High‑risk cardiovascular patients: Contributes to overall risk reduction when used as part of a comprehensive antihypertensive regimen.

How It Works

  • Olmesartan medoxomil selectively blocks angiotensin II type 1 (AT1) receptors, preventing vasoconstriction and aldosterone‑driven sodium retention. Hydrochlorothiazide acts on the distal convoluted tubule to inhibit NaCl reabsorption, increasing urinary sodium and water excretion. Together, they reduce peripheral resistance and plasma volume, producing an additive antihypertensive effect.

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 involving face, lips or airway
  • Liver function abnormalities
  • Blood dyscrasias such as agranulocytosis

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient history and monitor relevant parameters.

  • Renal function: Assess baseline creatinine and eGFR, adjust if impaired.
  • Electrolytes: Monitor serum potassium and sodium, especially when combined with other diuretics.
  • Pregnancy: Avoid use; potential risk to fetus.
  • Concomitant drugs: Review for interactions that affect potassium or renal function.
  • Elderly patients: Start at lower dose and monitor for orthostatic hypotension.
  • Store at ambient temperature: Keep below 25°C, in original packaging, protected from moisture.

Avoid Interactions

Olmesartan medoxomil/hydrochlorothiazide may interact with several drug classes; careful review is recommended.

Major Interactions (Avoid)

  • Aliskiren combined with concurrent ACE inhibitor or ARB therapy.
  • Potassium‑rich supplements or potassium‑sparing diuretics leading to hyperkalemia.
  • NSAIDs that may reduce antihypertensive efficacy and impair renal function.

Moderate Interactions (Monitor Closely)

  • Lithium: May increase serum lithium levels.
  • Antidiabetic agents: May require dose adjustment due to enhanced glucose lowering.
  • Other antihypertensives: May cause additive blood pressure reduction.
  • Corticosteroids: May potentiate electrolyte disturbances.
  • Antimicrobials such as trimethoprim‑sulfamethoxazole affecting potassium balance.

Frequently Asked Questions

Olmesartan Medoxomil E Idroclorotiazide Alter is a fixed‑dose combination of olmesartan medoxil, an angiotensin II receptor blocker, and hydrochlorothiazide, a thiazide diuretic. The product is prescribed to lower high blood pressure in adults, helping to reduce the risk of cardiovascular events such as stroke and heart attack.

Olmesartan medoxil blocks AT1 receptors, preventing angiotensin II‑mediated vasoconstriction and aldosterone release. Hydrochlorothiazide inhibits sodium‑chloride reabsorption in the distal tubule, increasing urine output. Together they lower peripheral vascular resistance and plasma volume, providing an additive antihypertensive effect.

The appropriate dose is determined by the prescribing clinician based on the patient’s blood pressure, renal function, and overall health status. Dosage adjustments are made individually, and patients should follow the prescriber’s instructions without self‑adjusting the amount.

Olmesartan medoxomil is classified as contraindicated during pregnancy because it can harm the developing fetus. Hydrochlorothiazide is also generally avoided. Breastfeeding mothers should consult their healthcare provider, as the drugs may pass into breast milk and affect the infant.

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, confirming trade or institutional credentials before providing pricing, availability, shipping details and any necessary import documentation.

Compared with single‑agent ARBs or thiazide diuretics, the fixed‑dose combination offers convenient dosing and synergistic blood‑pressure reduction. It may be preferred over separate tablets for patients needing both vasodilation and diuresis, while maintaining a similar safety profile to its individual components.

Store the tablets at ambient temperature, below 25 °C, in the original packaging. Protect them from moisture and direct sunlight to maintain potency throughout the shelf life.

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

Serious risks include severe hypotension, acute kidney injury, hyperkalemia, angio‑edema and liver function abnormalities. Patients should be monitored for signs such as dizziness, rapid weight loss, swelling of the face or throat, and changes in urine output, and seek medical attention promptly if they occur.

Individuals with known hypersensitivity to olmesartan, hydrochlorothiazide, or any component of the formulation should avoid this product. It is also contraindicated in pregnancy, patients with severe renal impairment, and those taking certain interacting drugs such as aliskiren or potassium‑sparing agents without medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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