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

Olmesartan Medoxomil/Amlodipine/Hydrochlorothiazide Krka

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

Olmesartan Medoxomil/Amlodipine/Hydrochlorothiazide Krka (Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide)

Olmesartan Medoxomil, the active ingredient in Olmesartan Medoxomil/Amlodipine/Hydrochlorothiazide Krka, is an angiotensin II receptor blocker presented as a tablet for oral use. It treats hypertension, often in combination with other antihypertensive agents, and is suitable for adult patients. GNH India supplies Olmesartan Medoxomil/Amlodipine/Hydrochlorothiazide Krka as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

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

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Olmesartan Medoxomil/Amlodipine/Hydrochlorothiazide is indicated for hypertension management, targeting the renin‑angiotensin system and calcium‑channel pathways.

  • Hypertension: provides combined blood pressure reduction through three complementary mechanisms.
  • High‑risk cardiovascular patients: helps achieve target blood pressure when monotherapy is insufficient.
  • Edema associated with hypertension therapy: mitigates fluid retention via the thiazide diuretic component.
  • Stroke prevention (adjunct): contributes to lower stroke risk by maintaining optimal blood pressure levels.
  • Chronic kidney disease with hypertension: assists in slowing renal function decline by controlling systemic pressure.

How It Works

  • The combination product works by three mechanisms: olmesartan medoxil blocks angiotensin II type 1 receptors, preventing vasoconstriction; amlodipine inhibits calcium influx into vascular smooth‑muscle cells, causing arterial dilation; and hydrochlorothiazide reduces sodium and water reabsorption in the distal convoluted tubule, decreasing plasma volume. Together these actions produce additive blood‑pressure‑lowering effects.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Dizziness or light‑headedness
  • Headache
  • Peripheral edema
  • Flushing
  • Fatigue
  • Cough

Serious or Rare Side Effects

  • Severe hypotension
  • Acute kidney injury
  • Electrolyte disturbances (e.g., hyponatremia, hyperkalemia)
  • Angio‑edema
  • Liver function abnormalities
  • Pancreatitis

Precautions & Warnings

When prescribing this combination, clinicians should consider several safety aspects.

  • Renal function monitoring: assess creatinine and electrolytes before and during therapy.
  • Hepatic impairment: use cautiously and adjust dose if needed.
  • Pregnancy: contraindicated in the second and third trimesters due to fetal toxicity.
  • Hyperkalemia risk: monitor serum potassium, especially when combined with potassium‑sparing agents.
  • Orthostatic hypotension: advise patients to rise slowly from sitting or lying positions.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Dual renin‑angiotensin system blockade (e.g., ACE inhibitors, other ARBs): increased risk of renal dysfunction and hyperkalemia.
  • Potassium‑rich supplements or potassium‑sparing diuretics: may cause dangerous hyperkalemia.
  • Strong CYP3A4 inhibitors (e.g., itraconazole, clarithromycin): elevate amlodipine levels, raising hypotension risk.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may blunt antihypertensive effect and affect renal function.
  • Lithium: concurrent use can increase lithium concentrations, risking toxicity.
  • Antidiabetic agents: may enhance glucose‑lowering effect, requiring dose adjustment.

Frequently Asked Questions

Olmesartan Medoxomil/Amlodipine/Hydrochlorothiazide is a fixed‑dose combination used to treat high blood pressure when a single‑agent regimen does not provide adequate control. It combines three antihypertensive mechanisms to lower systolic and diastolic pressures and reduce cardiovascular risk.

Olmesartan Medoxil blocks angiotensin II type‑1 receptors, preventing the hormone from causing blood‑vessel constriction and aldosterone release. This results in vasodilation and reduced fluid retention, contributing to overall blood‑pressure reduction when paired with amlodipine and hydrochlorothiazide.

The specific dose of Olmesartan Medoxomil/Amlodipine/Hydrochlorothiazide is determined by the prescribing clinician based on the patient’s blood‑pressure levels, comorbidities, and response to therapy. Dosage adjustments are made individually and are not standardized in public literature.

Olmesartan Medoxomil is contraindicated in the second and third trimesters of pregnancy because of potential fetal toxicity. Use during breastfeeding is not recommended unless the benefit outweighs the risk, and the decision should be made by a healthcare professional.

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, this triple‑component tablet offers broader blood‑pressure control by targeting the renin‑angiotensin system, calcium channels, and renal sodium handling simultaneously. It can simplify regimens and improve adherence, but clinicians must consider the higher potential for combined side effects versus single‑agent therapy.

Store the tablets at or below 25 °C in a dry place, protected from moisture and direct sunlight. Keep them in the original container to maintain stability and prevent accidental exposure to humidity.

The product is taken orally, usually once daily, with or without food, as directed by the prescribing physician. Swallow the tablet whole with a glass of water and follow any specific timing instructions provided by the healthcare provider.

Serious risks include severe hypotension, acute kidney injury, significant electrolyte disturbances such as hyper‑ or hyponatremia, and rare cases of angio‑edema. Patients should be monitored regularly for these events, especially when initiating therapy or adjusting doses.

Individuals with known hypersensitivity to any component of the combination, pregnant women in the second or third trimester, patients with severe hepatic impairment, and those taking other potent renin‑angiotensin system blockers should avoid this product unless specifically advised by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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