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

Olmesartan Medoxomil/Hydrochlorothiazide Msn

Active Ingredient:
Olmesartan Medoxomil, Hydrochlorothiazide
Origin:
EU

Olmesartan Medoxomil/Hydrochlorothiazide Msn (Olmesartan Medoxomil, Hydrochlorothiazide)

Olmesartan medoxomil, the active ingredient in Olmesartan Medoxomil/Hydrochlorothiazide Msn, is an angiotensin II receptor blocker (ARB) presented as a combination tablet for oral use. It treats hypertension, often in patients who require additional blood pressure control beyond what an ARB alone can provide.

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

Manufacturer / TM Owner

Msn Labs Europe Limited

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Indications & Clinical Uses

Olmesartan medoxomil/hydrochlorothiazide is used in the management of high blood pressure by targeting the renin‑angiotensin system and promoting diuresis.

  • Hypertension: lowers systolic and diastolic blood pressure when monotherapy is insufficient.
  • Resistant hypertension: provides additional blood pressure reduction in patients not controlled on single‑agent therapy.
  • Cardiovascular risk reduction: contributes to lower risk of stroke and heart attack in hypertensive patients when combined with lifestyle measures.

How It Works

  • Olmesartan medoxomil blocks the binding of angiotensin II to the AT‑1 receptor, preventing vasoconstriction and aldosterone release, while hydrochlorothiazide inhibits sodium‑chloride reabsorption in the distal convoluted tubule, increasing urinary water excretion. The combined actions produce additive reductions in peripheral vascular resistance and plasma volume, resulting in lowered 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
  • Angio‑edema
  • Severe electrolyte imbalance
  • Liver function abnormalities

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 potassium and sodium levels regularly.
  • Pregnancy: avoid use; teratogenic risk associated with ARBs.
  • 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, protect from moisture and light.

Avoid Interactions

Olmesartan medoxomil/hydrochlorothiazide can interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Aliskiren (in diabetic patients): risk of renal impairment and hyperkalemia.
  • Potassium‑sparing diuretics or supplements: may cause dangerous hyperkalemia.
  • NSAIDs (high dose or chronic): can blunt antihypertensive effect and worsen renal function.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs (dual renin‑angiotensin blockade): increased risk of hypotension and kidney injury.
  • Lithium: may increase lithium levels, risking toxicity.
  • Antidiabetic agents: may require dose adjustment due to enhanced glucose lowering.
  • Antihistamines: may increase risk of dizziness.
  • Antifungal azoles: can affect drug metabolism, requiring monitoring.

Frequently Asked Questions

Olmesartan Medoxomil/Hydrochlorothiazide is a fixed‑dose combination used to lower high blood pressure in adults, especially when a single antihypertensive agent does not provide adequate control.

Olmesartan medoxomil blocks the angiotensin II type‑1 (AT‑1) receptors, preventing vasoconstriction and aldosterone release, which helps relax blood vessels and reduce blood pressure.

The prescribed dose is individualized by a healthcare professional based on the patient’s blood pressure, response to therapy, and any existing medical conditions.

Olmesartan Medoxomil/Hydrochlorothiazide is contraindicated in pregnancy because ARBs can cause fetal toxicity. Caution is also advised during breastfeeding, and a clinician should evaluate the risk‑benefit ratio.

To place an order, submit an enquiry on the product page at gnhindia.com with 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 monotherapy ARBs or thiazide diuretics, the combination offers additive blood‑pressure reduction, allowing lower doses of each component and potentially fewer side effects than higher‑dose single agents.

Store the tablets at ambient temperature, below 25 °C, in the original container, protected from moisture and light to maintain stability.

The medication is taken orally, usually once daily, with or without food, as directed by a healthcare professional.

Serious risks include severe hypotension, acute kidney injury, hyperkalemia, and angio‑edema. Patients should be monitored for signs such as dizziness, rapid weight gain, swelling, or difficulty breathing.

Individuals with known hypersensitivity to olmesartan, hydrochlorothiazide, or any component of the formulation, as well as pregnant women, should avoid this medication.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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