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

Olmesartán/Amlodipino/Hidroclorotiazida Stada

Active Ingredient:
Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide
Origin:
EU

Olmesartán/Amlodipino/Hidroclorotiazida Stada (Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide)

Olmesartan medoxil, amlodipine, hydrochlorothiazide, the active ingredients in Olmesartán/Amlodipino/Hidroclorotiazida Stada, is a combination antihypertensive presented as a tablet for oral use. It treats high blood pressure in adults, often when single‑agent therapy is insufficient.

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

Manufacturer / TM Owner

Laboratorio Stada, S.L.

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Indications & Clinical Uses

Olmesartan/Amlodipine/Hydrochlorothiazide is used in the management of hypertension, targeting multiple pathways that control blood pressure.

  • Hypertension: lowers systolic and diastolic pressure when monotherapy does not achieve target levels.
  • Resistant hypertension: provides additional control in patients who need more than one class of antihypertensive.
  • Cardiovascular risk reduction: contributes to lowering the risk of stroke and myocardial infarction associated with high blood pressure.

How It Works

  • The combination works through three complementary mechanisms: olmesartan blocks the angiotensin II type‑1 receptor, reducing vasoconstriction and aldosterone release; amlodipine inhibits calcium influx into vascular smooth‑muscle cells, causing arterial dilation; and hydrochlorothiazide promotes renal sodium and water excretion, decreasing plasma volume. Together these actions produce additive blood‑pressure reduction.

Side Effects

Adverse reactions may occur with any antihypertensive combination therapy.

Common Side Effects

  • Dizziness or light‑headedness
  • Headache
  • Peripheral edema
  • Fatigue
  • Cough
  • Increased urination

Serious or Rare Side Effects

  • Severe hypotension
  • Electrolyte disturbances (e.g., low potassium)
  • Acute kidney injury
  • Angio‑edema
  • Liver enzyme elevation
  • Blood cell abnormalities

Precautions & Warnings

Before initiating therapy, consider patient‑specific factors and monitor appropriately.

  • Renal impairment: adjust monitoring of kidney function and electrolytes.
  • Hepatic disease: use with caution; monitor liver enzymes.
  • Electrolyte imbalance: watch for potassium and sodium levels.
  • Pregnancy: avoid use; teratogenic risk is unknown.
  • Elderly patients: start at lower dose and monitor for orthostatic hypotension.
  • Store at below 25°C: keep in the original container, protect from moisture and light.

Avoid Interactions

Olmesartan/Amlodipine/Hydrochlorothiazide may interact with several drug classes.

Major Interactions (Avoid)

  • Dual renin‑angiotensin system blockade (e.g., ACE inhibitors, other ARBs): risk of hyperkalaemia and renal failure.
  • Potassium‑sparing diuretics or supplements: may cause dangerous hyperkalaemia.
  • Strong CYP3A4 inhibitors (e.g., clarithromycin, itraconazole): increase amlodipine levels.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may reduce antihypertensive effect and impair renal function.
  • Lithium: may increase lithium levels, risking toxicity.
  • Antidiabetic agents: may enhance hypoglycaemia; monitor glucose.
  • Alcohol: additive blood‑pressure lowering effect; advise moderation.

Frequently Asked Questions

Olmesartan/Amlodipine/Hydrochlorothiazide is a fixed‑dose combination antihypertensive used to lower high blood pressure, especially when a single agent does not achieve target levels or in cases of resistant hypertension.

Olmesartan blocks the angiotensin II type‑1 receptor, preventing vasoconstriction and reducing aldosterone‑mediated sodium retention, which helps to lower systemic vascular resistance and blood pressure.

The prescribed dose is determined by the treating physician based on the patient’s blood‑pressure goals, renal function, and tolerance. Dosage adjustments are made individually and should follow the prescriber’s instructions.

Use during pregnancy is not recommended because the safety of the combination has not been established and there may be fetal risk. Breastfeeding mothers should consult a healthcare professional before use.

Submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and import documentation.

Compared with single‑agent therapy, the three‑component blend offers additive blood‑pressure reduction by targeting the renin‑angiotensin system, calcium‑channel mediated vasodilation, and diuresis, often achieving better control than monotherapy while simplifying dosing.

Store the tablets at or below 25 °C in the original packaging, protected from moisture and direct light. Do not store in a humid environment or expose to extreme temperatures.

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

Serious risks include severe hypotension, electrolyte disturbances such as hyperkalaemia, acute kidney injury, angio‑edema, and rare liver enzyme elevations. Patients should be monitored for these events, especially when initiating therapy.

Patients with known hypersensitivity to any component, those with severe renal or hepatic impairment, pregnant women, and individuals on concurrent dual renin‑angiotensin blockade should avoid this product unless specifically directed by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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