Product image of Olmesartan Medoxomilo + Hidroclorotiazida Jubilant (Olmesartan Medoxomil, Hydrochlorothiazide) supplied by GNH India

Olmesartan Medoxomilo + Hidroclorotiazida Jubilant

Active Ingredient:
Olmesartan Medoxomil, Hydrochlorothiazide
Origin:
EU

Olmesartan Medoxomilo + Hidroclorotiazida Jubilant (Olmesartan Medoxomil, Hydrochlorothiazide)

Olmesartan medoxil, the active ingredient in Olmesartan Medoxomilo + Hidroclorotiazida Jubilant, is an angiotensin II receptor blocker presented as a tablet for oral use. It is used to manage high blood pressure, often in combination with a diuretic, and is prescribed for adults.

GNH India supplies Olmesartan Medoxomilo + Hidroclorotiazida Jubilant as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Jubilant Pharmaceuticals Nv

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Indications & Clinical Uses

Olmesartan medoxil combined with hydrochlorothiazide is indicated for hypertension management within the renin‑angiotensin‑aldosterone system pathway.

  • Essential hypertension: lowers systolic and diastolic blood pressure to reduce cardiovascular risk.
  • Hypertension with fluid retention: provides additional diuretic effect to improve blood pressure control.
  • High‑risk cardiovascular patients: assists in achieving target blood pressure when monotherapy is insufficient.

How It Works

  • Olmesartan medoxil selectively blocks the binding of angiotensin II to the AT1 receptor on vascular smooth‑muscle and adrenal cells, preventing vasoconstriction and aldosterone release. Hydrochlorothiazide inhibits sodium‑chloride reabsorption in the distal convoluted tubule, promoting diuresis and further decreasing plasma volume, which together produce a synergistic antihypertensive effect.

Side Effects

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

Common Side Effects

  • Dizziness or light‑headedness
  • Headache
  • Fatigue
  • Cough
  • Increased urination
  • Electrolyte disturbances (e.g., low potassium)

Serious or Rare Side Effects

  • Severe hypotension
  • Acute kidney injury
  • Hyperkalemia
  • Angio‑edema
  • Liver function abnormalities
  • Blood dyscrasias such as agranulocytosis

Precautions & Warnings

Before initiating therapy, clinicians should assess patient history and monitor relevant parameters.

  • Renal function: evaluate baseline creatinine and eGFR.
  • Electrolytes: check serum potassium and sodium levels.
  • Hepatic function: monitor liver enzymes in patients with liver disease.
  • Pregnancy: avoid use; drug is contraindicated in the second and third trimesters.
  • Concomitant NSAIDs: use with caution as they may reduce antihypertensive effect.
  • Store at ambient temperature: keep below 25°C, retain in original packaging, and protect from moisture.

Avoid Interactions

Olmesartan medoxil + hydrochlorothiazide may interact with several drug classes, requiring clinical vigilance.

Major Interactions (Avoid)

  • Aliskiren (dual renin‑angiotensin system blockade increases risk of renal impairment).
  • Potassium‑sparing diuretics or supplements (risk of hyperkalemia).
  • Lithium (reduced clearance may lead to toxicity).

Moderate Interactions (Monitor Closely)

  • NSAIDs (may blunt antihypertensive response and affect renal function).
  • ACE inhibitors (combined use can cause additive hypotension and hyperkalemia).
  • Antidiabetic agents (diuretic effect may enhance hypoglycaemia).

Frequently Asked Questions

Olmesartan Medoxomilo + Hidroclorotiazida Jubilant is a fixed‑dose combination of olmesartan medoxil and hydrochlorothiazide indicated for the treatment of hypertension, including cases where additional diuretic therapy is needed to achieve blood‑pressure targets.

Olmesartan medoxil is an angiotensin II receptor blocker that selectively inhibits AT‑1 receptors, preventing vasoconstriction and aldosterone‑mediated sodium retention, which together lower blood pressure.

The prescribed dose is determined by the treating physician based on the patient’s blood‑pressure readings, renal function, and overall clinical profile; dosing instructions are not standardized in public literature.

Olmesartan‑containing products are contraindicated in pregnancy, especially during the second and third trimesters, due to risk of fetal toxicity. Limited data exist for breastfeeding, so use is generally discouraged unless the benefit outweighs potential risk.

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.

The olmesartan‑hydrochlorothiazide combo offers dual mechanisms—angiotensin‑II blockade and diuresis—providing more potent blood‑pressure reduction than either agent alone. It is often preferred over monotherapy when patients need additional control, but alternatives such as ACE‑inhibitor/diuretic combos may be chosen based on tolerance and comorbidities.

Store the tablets at ambient temperature, below 25 °C, in the original container to protect from moisture and light. Do not refrigerate or freeze the product.

The medication is taken orally, usually once daily, with or without food, as directed by the prescribing clinician.

Serious adverse events include severe hypotension, acute kidney injury, hyperkalemia, angio‑edema and liver‑function abnormalities. Patients should be monitored regularly for these conditions, especially during therapy initiation or dose changes.

Individuals with known hypersensitivity to olmesartan, hydrochlorothiazide or any excipients, pregnant women (second and third trimesters), patients with severe renal impairment, and those taking contraindicated drugs such as aliskiren in combination with an ARB should avoid this product.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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