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

Olmesartan/Amlodipine/Hctz Krka

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

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

Olmesartan medoxil, the active ingredient in Olmesartan/Amlodipine/Hctz Krka, is an angiotensin II receptor blocker (ARB) presented as a combination tablet for oral use. It treats hypertension, often in patients who require multiple mechanisms to control blood pressure. GNH India supplies Olmesartan/Amlodipine/Hctz Krka as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

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

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Olmesartan/Amlodipine/Hctz combines three agents that act on the renin‑angiotensin system and vascular smooth‑muscle tone to lower blood pressure.

  • Hypertension: provides combined blockade of angiotensin II receptors, calcium‑channel mediated vasodilation, and diuresis to achieve target blood‑pressure control.
  • Resistant hypertension: adds a thiazide‑type diuretic to an ARB/CCB regimen when monotherapy or dual therapy is insufficient.
  • Hypertension with edema: amlodipine‑induced peripheral edema is mitigated by the diuretic component, improving tolerability.

How It Works

  • Olmesartan medoxomil selectively blocks the binding of angiotensin II to AT1 receptors, preventing vasoconstriction and aldosterone release. Amlodipine inhibits calcium influx into vascular smooth‑muscle cells, causing arterial dilation. Hydrochlorothiazide reduces sodium and water reabsorption in the distal convoluted tubule, decreasing plasma volume. The three mechanisms act synergistically to lower systemic vascular resistance and cardiac output, resulting in sustained blood‑pressure reduction.

Side Effects

Adverse reactions may range from mild to severe and should be monitored during therapy.

Common Side Effects

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

Serious or Rare Side Effects

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

Precautions & Warnings

Before initiating therapy, clinicians should assess individual risk factors and monitor relevant parameters.

  • Renal function: evaluate baseline creatinine and eGFR, adjust if impaired.
  • Electrolytes: check potassium and sodium levels, especially with diuretic use.
  • Pregnancy: contraindicated in the second and third trimesters; avoid unless clearly needed.
  • Concomitant drugs: review for potential additive blood‑pressure lowering effects.
  • Elderly patients: start at lower dose and monitor for orthostatic symptoms.
  • Store at ambient temperature: keep tablets in original container, protect from moisture and direct sunlight.

Avoid Interactions

Olmesartan/Amlodipine/Hctz may interact with several drug classes; careful review is essential.

Major Interactions (Avoid)

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

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may blunt antihypertensive effect and affect renal function.
  • Lithium: can increase lithium concentrations, risking toxicity.
  • Antidiabetic agents: may enhance glucose‑lowering effect, requiring dose adjustment.
  • Alcohol: additive vasodilatory effect may increase dizziness.
  • Digoxin: monitor levels as electrolyte shifts can affect cardiac conduction.

Frequently Asked Questions

Olmesartan/Amlodipine/Hctz Krka is a fixed‑dose combination tablet indicated for the treatment of hypertension, including cases that are resistant to single‑agent therapy. The three components work together to lower blood pressure by blocking angiotensin II, dilating blood vessels, and promoting diuresis.

Olmesartan medoxil is an angiotensin II receptor blocker that selectively inhibits AT1 receptors, preventing vasoconstriction and aldosterone‑mediated sodium retention. In the combination, it provides the primary renin‑angiotensin system blockade that complements the vasodilatory effect of amlodipine and the diuretic action of hydrochlorothiazide.

The specific dose of Olmesartan/Amlodipine/Hctz Krka is determined by the prescribing clinician based on the patient’s blood‑pressure level, prior therapy, and renal function. Healthcare professionals select the appropriate strength and titrate according to clinical response.

Olmesartan/Amlodipine/Hctz Krka is generally contraindicated in pregnancy, especially in the second and third trimesters, because angiotensin‑II blockade can harm the fetus. Use during breastfeeding is not recommended unless the benefit outweighs potential risk; consultation with a healthcare provider is essential.

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, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Compared with single‑agent therapy, the Olmesartan/Amlodipine/Hctz combination offers synergistic blood‑pressure reduction, potentially improving control in patients who need multiple mechanisms. It may be preferred over separate tablets for adherence, but clinicians consider individual tolerability, renal function and electrolyte balance when selecting therapy.

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

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Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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