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

Olsitri

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

Olsitri (Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide)

Olmesartan medoxomil, amlodipine and hydrochlorothiazide, the active ingredients in Olsitri, are a combination antihypertensive presented as a tablet for oral use. It treats essential hypertension in adult patients.

GNH India supplies Olsitri 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

  • Olsitri, a combination antihypertensive, is indicated for conditions related to elevated blood pressure.
  • Essential hypertension: lowers systolic and diastolic pressure in patients with primary hypertension.
  • Isolated systolic hypertension: reduces high systolic readings in older adults.
  • Hypertension requiring triple therapy: provides three complementary mechanisms for patients not controlled on single or dual agents.

How It Works

  • Olmesartan medoxomil blocks angiotensin II AT1 receptors, reducing vasoconstriction and aldosterone release. Amlodipine inhibits calcium influx into vascular smooth muscle, producing arterial vasodilation. Hydrochlorothiazide acts on the distal convoluted tubule to inhibit sodium‑chloride reabsorption, increasing diuresis and decreasing plasma volume. Together, the three agents produce additive blood‑pressure‑lowering effects through vascular relaxation, reduced fluid retention, and inhibition of the renin‑angiotensin system.

Side Effects

Common Side Effects

  • Dizziness or light‑headedness
  • Headache
  • Peripheral edema, especially of the ankles
  • Flushing or warmth sensation
  • Fatigue or mild weakness
  • Increased urinary frequency

Serious or Rare Side Effects

  • Severe hypotension or syncope
  • Electrolyte disturbances such as hyperkalemia, hyponatremia, or hypokalemia
  • Acute kidney injury or worsening renal function
  • Angioedema or severe allergic reactions
  • Liver enzyme elevation or hepatitis
  • Blood dyscrasias such as leukopenia or thrombocytopenia

Precautions & Warnings

Before initiating Olsitri, clinicians should consider several safety aspects.

  • Blood pressure monitoring: ensure adequate control and avoid excessive drops.
  • Renal function assessment: check serum creatinine and eGFR, especially in patients with pre‑existing kidney disease.
  • Electrolyte surveillance: monitor potassium and sodium levels due to the thiazide component.
  • Hepatic impairment: use with caution in patients with liver disease as metabolism may be altered.
  • Hypersensitivity: discontinue if signs of rash, angioedema, or anaphylaxis appear.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Olsitri may interact with several medicines that affect blood pressure, electrolytes, or drug metabolism.

Major Interactions (Avoid)

  • Concomitant use with aliskiren in diabetic patients: risk of renal impairment and hyperkalemia.
  • Dual renin‑angiotensin system blockade (ACE inhibitor or another ARB): may cause severe hypotension and kidney injury.
  • Potassium‑sparing diuretics (e.g., spironolactone): increase risk of hyperkalemia.
  • Strong CYP3A4 inhibitors (e.g., clarithromycin, itraconazole): raise amlodipine plasma levels.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may blunt antihypertensive effect and affect renal function.

Moderate Interactions (Monitor Closely)

  • Other antihypertensives (beta‑blockers, ACE inhibitors): additive blood‑pressure lowering.
  • Lithium: thiazide component can raise lithium concentrations.
  • Digoxin: possible increase in serum digoxin levels.
  • Additional thiazide diuretics: heightened electrolyte disturbances.
  • Alcohol: may enhance hypotensive effect.

Frequently Asked Questions

Olsitri is a prescription medication that combines olmesartan, amlodipine and hydrochlorothiazide to lower high blood pressure. It is primarily indicated for essential hypertension, including cases that need more than one class of antihypertensive agents to achieve target blood‑pressure levels.

Olmesartan blocks angiotensin II receptors, reducing vasoconstriction and aldosterone release. Amlodipine relaxes arterial smooth muscle by inhibiting calcium entry, causing vasodilation. Hydrochlorothiazide promotes sodium and water excretion in the kidneys, decreasing plasma volume. Together they provide complementary mechanisms that lower both systolic and diastolic pressures.

The specific dose of Olsitri is determined by the prescribing clinician based on the patient’s blood‑pressure readings, renal function, and overall health status. Dosage adjustments are made individually, and patients should follow the exact regimen written on their prescription.

Olsitri is generally not recommended for use during pregnancy because the components may affect fetal development, especially the angiotensin‑II blocker. Breastfeeding mothers should consult their healthcare provider, as the drugs can be excreted in breast milk and may pose risks to the infant.

To request Olsitri, 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 therapies, Olsitri offers three complementary mechanisms in one tablet, which can improve blood‑pressure control and simplify dosing. It may be preferred over separate pills when patients need an ARB, a calcium‑channel blocker and a thiazide diuretic together, reducing pill burden and improving adherence.

Olsitri tablets should be stored at ambient temperature, below 25 °C, in the original blister pack or container. Keep them away from moisture, direct sunlight and heat sources to maintain stability and potency throughout the shelf life.

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

The most serious risks include severe hypotension, electrolyte imbalances (especially low sodium or potassium), acute kidney injury, angioedema and liver dysfunction. Patients should be monitored regularly for these events, and any sudden dizziness, swelling of the face or throat, or abnormal lab results should prompt immediate medical evaluation.

Olsitri should be avoided in individuals with known hypersensitivity to any of its components, severe renal impairment, severe hepatic disease, or in patients who are pregnant. It is also contraindicated in patients taking aliskiren together with an ACE inhibitor or ARB if they have diabetes.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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