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

Olmesartan/Amlodipin/Hydrochlorthiazid Krka

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

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

Olmesartan medoxil, the active ingredient in Olmesartan/Amlodipin/Hydrochlorthiazid Krka, is a 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/Amlodipin/Hydrochlorthiazid Krka as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Olmesartan/Amlodipin/Hydrochlorthiazid Krka is manufactured by Krka and marketed as a fixed‑dose combination therapy for high blood pressure.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Olmesartan/Amlodipin/Hydrochlorthiazid Krka is used in the management of hypertension, targeting the renin‑angiotensin system and vascular smooth‑muscle tone.

  • Hypertension: lowers systolic and diastolic blood pressure to reduce cardiovascular risk.
  • Hypertensive urgency: provides rapid, controlled reduction of elevated blood pressure when immediate treatment is required.
  • Resistant hypertension: adds complementary mechanisms to achieve target blood pressure when monotherapy is insufficient.

How It Works

  • The combination product contains three agents that act synergistically: olmesartan medoxil blocks the angiotensin II type‑1 receptor, preventing vasoconstriction; amlodipine inhibits calcium influx into vascular smooth‑muscle cells, producing arterial dilation; and hydrochlorothiazide promotes renal excretion of sodium and water, decreasing plasma volume. Together they lower peripheral resistance and cardiac output, resulting in sustained blood‑pressure reduction.

Side Effects

Side effects may occur with any antihypertensive regimen and vary in frequency.

Common Side Effects

  • Dizziness or light‑headedness, especially after the first doses.
  • Peripheral edema, often noticeable in the ankles.
  • Headache, typically mild and transient.
  • Flushing or warmth sensation.
  • Fatigue or general tiredness.
  • Increased urination due to the diuretic component.

Serious or Rare Side Effects

  • Severe hypotension leading to fainting.
  • Acute kidney injury manifested by sudden rise in creatinine.
  • Electrolyte disturbances such as low potassium or sodium.
  • Angio‑edema affecting the face, lips or airway.
  • Liver enzyme elevations indicating hepatic stress.
  • Allergic reactions ranging from rash to anaphylaxis.

Precautions & Warnings

When prescribing Olmesartan/Amlodipin/Hydrochlorthiazid Krka, clinicians should consider several safety aspects.

  • Monitor blood pressure: ensure adequate control without excessive lowering.
  • Assess renal function: check creatinine and electrolytes before and during therapy.
  • Evaluate electrolytes: watch for hyponatremia or hypokalemia, especially with the thiazide component.
  • Review cardiac status: caution in patients with severe aortic stenosis or heart failure.
  • Pregnancy and lactation: avoid use; teratogenic risk is recognized for ARBs.
  • Store at ambient temperature: keep below 25°C, protect from moisture and light, retain in original packaging.

Avoid Interactions

Olmesartan/Amlodipin/Hydrochlorthiazid Krka can interact with several other medicines; awareness helps prevent adverse events.

Major Interactions (Avoid)

  • Concomitant use with aliskiren in patients with diabetes or renal impairment.
  • Potassium‑rich supplements or potassium‑sparing diuretics, which may cause hyper‑kalemia.
  • Strong CYP3A4 inhibitors (e.g., itraconazole, clarithromycin) that increase amlodipine levels.

Moderate Interactions (Monitor Closely):

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) that may blunt antihypertensive effect.
  • Lithium, as thiazides reduce renal clearance and raise lithium concentrations.
  • Antidiabetic agents, since blood‑pressure reduction can enhance glucose‑lowering effects.
  • Alcohol, which may increase dizziness and hypotensive response.
  • Other antihypertensives, requiring dose adjustments to avoid excessive blood‑pressure fall.

Frequently Asked Questions

Olmesartan/Amlodipin/Hydrochlorthiazid Krka is a fixed‑dose combination tablet indicated for the treatment of hypertension, including cases that require more than one mechanism of action to achieve target blood‑pressure levels.

Olmesartan medoxil blocks the angiotensin II type‑1 receptor, preventing vasoconstriction and aldosterone release. In the combination, it works together with amlodipine‑induced arterial dilation and hydrochlorothiazide‑driven diuresis to lower peripheral resistance and blood volume.

The appropriate dose is determined by the prescribing clinician based on the patient’s blood‑pressure readings, renal function, and overall treatment plan. Dosage adjustments are made according to therapeutic response and tolerability.

Olmesartan/Amlodipin/Hydrochlorthiazid Krka is contraindicated in pregnancy because angiotensin‑II receptor blockers can cause fetal toxicity. Breastfeeding is not recommended as the safety profile for the combination has not been established.

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, this triple‑component tablet offers synergistic blood‑pressure control, reducing the need for multiple pills. It is often preferred over separate prescriptions when patients need both an ARB, a calcium‑channel blocker, and a thiazide diuretic, providing convenience and improved adherence.

Store the tablets at ambient temperature, preferably below 25 °C, in the original container protected from moisture and light. Avoid extreme heat or humidity to maintain product stability.

The medication is taken orally, usually once daily, with or without food, as directed by the healthcare professional. Swallow the tablet whole with a glass of water; do not crush or chew unless specifically instructed.

Serious risks include severe hypotension, acute kidney injury, electrolyte imbalances (especially low potassium), and angio‑edema. Patients should be monitored for signs of these conditions, and therapy should be stopped immediately if they occur.

The product should be avoided in patients with known hypersensitivity to any component, in pregnant women, and in individuals with severe renal impairment, significant aortic stenosis, or uncontrolled heart failure unless specifically directed by a specialist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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