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

Olmesartan/Amlodipin/Hct Ratiopharm

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

Olmesartan/Amlodipin/Hct Ratiopharm (Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide)

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

Olmesartan/Amlodipin/Hct Ratiopharm is provided by GNH India, a certified supplier adhering to global quality standards.

Manufacturer / TM Owner

Ratiopharm Gmbh

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Indications & Clinical Uses

Olmesartan/Amlodipin/Hct Ratiopharm is indicated for hypertension management, acting on the renin‑angiotensin system and vascular smooth‑muscle tone.

  • Essential hypertension: lowers systolic and diastolic blood pressure to reduce cardiovascular risk.
  • Hypertension with fluid retention: combines vasodilation with diuretic action to improve blood‑pressure control.
  • Hypertension in patients requiring multiple mechanisms: provides triple‑mechanism therapy (ARB, calcium‑channel blocker, thiazide diuretic).

How It Works

  • Olmesartan medoxil blocks the binding of angiotensin II to AT‑1 receptors, preventing vasoconstriction. 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 combined actions produce additive blood‑pressure reduction.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Headache
  • Peripheral edema
  • Dizziness
  • Flushing
  • Fatigue
  • Increased urination

Serious or Rare Side Effects

  • Angio‑edema
  • Severe hypotension
  • Electrolyte disturbances (e.g., hyponatremia, hypokalemia)
  • Acute kidney injury
  • Liver enzyme elevation
  • Blood dyscrasias

Precautions & Warnings

When prescribing Olmesartan/Amlodipin/Hct Ratiopharm, clinicians should consider several safety aspects.

  • Renal function monitoring: assess baseline creatinine and eGFR, especially in patients with chronic kidney disease.
  • Electrolyte assessment: check serum potassium and sodium levels regularly.
  • Pregnancy contraindication: avoid use in pregnancy due to fetal toxicity.
  • Concomitant drug review: evaluate for other antihypertensives that may cause additive hypotension.
  • Patient education: advise on signs of low blood pressure and when to seek medical help.
  • Store at ambient temperature: keep below 25°C, retain in original packaging, protect from moisture.

Avoid Interactions

Olmesartan/Amlodipin/Hct Ratiopharm may interact with several medicines; careful review is required.

Major Interactions (Avoid)

  • Dual renin‑angiotensin system blockade (e.g., ACE inhibitors, aliskiren) – increased risk of renal impairment and hyperkalaemia.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole) – may raise amlodipine levels.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) – may blunt antihypertensive effect and affect renal function.
  • Lithium – increased lithium concentrations, risk of toxicity.
  • Digoxin – heightened risk of digoxin toxicity when combined with diuretics.
  • High‑dose potassium supplements – may exacerbate hyperkalaemia.
  • Alcohol – additive vasodilatory effect, may increase dizziness.

Frequently Asked Questions

Olmesartan/Amlodipin/Hct Ratiopharm is a fixed‑dose combination tablet that treats high blood pressure. It combines an angiotensin‑II receptor blocker, a calcium‑channel blocker, and a thiazide diuretic to lower systolic and diastolic pressures in adults with hypertension, including cases where fluid retention is present.

Olmesartan medoxil blocks AT‑1 receptors, preventing angiotensin II‑mediated vasoconstriction. This action relaxes blood vessels, reducing peripheral resistance and lowering blood pressure. In the combination product, amlodipine adds arterial dilation and hydrochlorothiazide promotes sodium‑water excretion, providing complementary mechanisms.

The dose of Olmesartan/Amlodipin/Hct Ratiopharm is individualized by the prescribing clinician based on the patient’s blood‑pressure level, response, and tolerability. The prescriber determines the appropriate strength and titration schedule according to clinical guidelines.

Olmesartan/Amlodipin/Hct Ratiopharm is contraindicated in pregnancy because angiotensin‑II receptor blockers can cause fetal toxicity. Breastfeeding is not recommended without medical advice, as the components may pass into milk and affect the infant. Consultation with a healthcare professional 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 required import documentation.

Compared with single‑agent therapy, the Olmesartan/Amlodipin/Hct combination offers three complementary mechanisms in one tablet, which can improve blood‑pressure control and simplify regimens. Alternatives may include separate ARB, calcium‑channel blocker, or diuretic tablets, but the fixed‑dose format reduces pill burden and may enhance adherence.

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

The medication is taken orally, usually once daily, with or without food, as directed by the prescribing clinician. Swallow the tablet whole; do not crush or chew unless specifically instructed.

Serious adverse events include angio‑edema, severe hypotension, significant electrolyte disturbances, and acute kidney injury. Patients should be monitored for signs such as swelling of the face or throat, dizziness, rapid weight loss, or reduced urine output, and seek immediate medical attention if they occur.

Individuals with known hypersensitivity to any component, pregnant women, and patients with severe renal impairment or uncontrolled electrolyte abnormalities should not use this product. Clinicians should also exercise caution in patients on multiple renin‑angiotensin system inhibitors.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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