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

Olmesartán/Amlodipino/Hidroclorotiazida Viso Farmacéutica

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

Olmesartán/Amlodipino/Hidroclorotiazida Viso Farmacéutica (Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide)

Olmesartan medoxil, amlodipine, hydrochlorothiazide, the active ingredients in Olmesartán/Amlodipino/Hidroclorotiazida Viso Farmacéutica, is a combination antihypertensive presented as a tablet for oral use. It treats hypertension, often in patients who require more than one mechanism to control blood pressure. GNH India supplies Olmesartán/Amlodipino/Hidroclorotiazida Viso Farmacéutica as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

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

Manufacturer / TM Owner

Glenmark Arzneimittel Gmbh

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Indications & Clinical Uses

Olmesartan/Amlodipine/Hydrochlorothiazide is a fixed‑dose combination that acts on several pathways involved in blood‑pressure regulation.

  • Hypertension: provides additive blood‑pressure reduction when monotherapy is insufficient.
  • High‑risk cardiovascular patients: helps achieve target blood pressure to lower risk of stroke and myocardial infarction.
  • Patients with fluid retention: adds diuretic effect to improve volume control alongside vasodilation and renin‑angiotensin blockade.

How It Works

  • The combination pairs an angiotensin‑II receptor blocker (olmesartan) that blocks AT1 receptors, a calcium‑channel blocker (amlodipine) that relaxes vascular smooth muscle, and a thiazide‑type diuretic (hydrochlorothiazide) that promotes renal sodium and water excretion. Together they lower systemic vascular 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

  • Headache: mild to moderate intensity.
  • Peripheral edema: swelling of ankles or feet.
  • Dizziness or light‑headedness: especially after the first doses.
  • Flushing: transient warmth or redness.
  • Fatigue: general tiredness.
  • Increased urination: due to the diuretic component.

Serious or Rare Side Effects

  • Angio‑edema: swelling of lips, tongue or airway.
  • Severe hypotension: marked drop in blood pressure causing fainting.
  • Electrolyte disturbances: significant changes in potassium or sodium levels.
  • Acute kidney injury: sudden decline in renal function.
  • Hepatic dysfunction: abnormal liver enzymes.
  • Blood dyscrasias: rare blood‑cell abnormalities.

Precautions & Warnings

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

  • Renal impairment: adjust dose or avoid if severe.
  • Hepatic disease: use with caution; monitor liver function.
  • Electrolyte imbalance: check potassium and sodium levels regularly.
  • Pregnancy: contraindicated in the second and third trimesters; avoid unless clearly needed.
  • Elderly patients: start at lower dose and titrate slowly.
  • Store at ambient temperature: keep below 25°C, retain in original packaging, protect from moisture and light.

Avoid Interactions

Olmesartan/Amlodipine/Hydrochlorothiazide may interact with several drug classes; awareness helps prevent adverse events.

Major Interactions (Avoid)

  • Potassium‑saving diuretics or supplements: risk of hyperkalaemia.
  • Strong CYP3A4 inhibitors (e.g., clarithromycin): increase amlodipine levels.
  • NSAIDs (high dose): may blunt antihypertensive effect and affect renal function.

Moderate Interactions (Monitor Closely)

  • Lithium: may increase serum lithium concentrations.
  • Other antihypertensives: additive blood‑pressure lowering effect.
  • Antidiabetic agents: may enhance glucose‑lowering effect.
  • Alcohol: can increase dizziness and hypotension risk.

Frequently Asked Questions

Olmesartan/Amlodipine/Hydrochlorothiazide is a fixed‑dose combination indicated for the treatment of hypertension, especially in patients who need more than one mechanism to achieve target blood pressure and in those with associated fluid retention.

Olmesartan is an angiotensin‑II receptor blocker that selectively blocks AT1 receptors, preventing angiotensin‑II‑mediated vasoconstriction and aldosterone release, which helps lower systemic vascular resistance and blood pressure.

The appropriate dose is determined by the prescribing clinician based on the patient’s blood‑pressure goals, renal function, and tolerance; dosing regimens are not disclosed here.

Use is contraindicated in the second and third trimesters of pregnancy because of potential fetal harm, and it should be used only if clearly needed while breastfeeding, after careful risk‑benefit assessment by a healthcare professional.

Submit an enquiry on the product page at gnhindia.com with 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 triple combination offers additive blood‑pressure reduction by targeting the renin‑angiotensin system, calcium channels, and fluid volume, often achieving better control with a single tablet and improving adherence versus multiple separate pills.

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

The product is taken orally, usually once daily with or without food, as directed by the prescribing healthcare professional.

Serious risks include angio‑edema, severe hypotension, electrolyte disturbances, acute kidney injury, and rare blood‑cell abnormalities; patients should be monitored for these events, especially during treatment initiation.

Patients with known hypersensitivity to any component, severe renal or hepatic impairment, or those in the second or third trimester of pregnancy should avoid this combination, as should anyone taking contraindicated interacting medicines.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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