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

Olmesartan Medoxomilo + Hidroclorotiazida Tolife

Active Ingredient:
Olmesartan Medoxomil, Hydrochlorothiazide
Origin:
EU

Olmesartan Medoxomilo + Hidroclorotiazida Tolife (Olmesartan Medoxomil, Hydrochlorothiazide)

Olmesartan medoxil and hydrochlorothiazide, the active ingredient in Olmesartan Medoxomilo + Hidroclorotiazida Tolife, is an Angiotensin II receptor blocker and thiazide diuretic presented as a combined oral tablet for systemic use. It treats hypertension in adult patients.

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

Manufacturer / TM Owner

Towa Pharmaceutical S.A.

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Indications & Clinical Uses

Olmesartan Medoxil combined with Hydrochlorothiazide is used to manage high blood pressure by targeting the renin‑angiotensin system and promoting diuresis.

  • Hypertension: lowers systolic and diastolic blood pressure in patients with primary hypertension.
  • Resistant hypertension: provides additional blood‑pressure control when monotherapy is insufficient.
  • Hypertension with fluid retention: reduces plasma volume and vascular resistance, improving overall control.

How It Works

  • Olmesartan medoxil selectively blocks AT1 receptors, preventing angiotensin II‑mediated vasoconstriction and aldosterone release, while hydrochlorothiazide inhibits NaCl reabsorption in the distal convoluted tubule, increasing urinary excretion of sodium and water. The combined effect reduces peripheral vascular resistance and plasma volume, leading to sustained blood‑pressure reduction.

Side Effects

Common Side Effects

  • Dizziness: transient light‑headedness, especially after the first doses.
  • Headache: mild to moderate intensity, often resolves with continued therapy.
  • Increased urination: due to the diuretic component, may be noticeable initially.
  • Electrolyte imbalance: mild reductions in potassium or sodium levels.

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips, tongue, or airway requiring immediate medical attention.
  • Severe dehydration: excessive fluid loss leading to hypotension.
  • Acute kidney injury: sudden decline in renal function, especially in patients with pre‑existing kidney disease.
  • Hyperkalemia: elevated potassium levels, potentially dangerous if untreated.
  • Severe hypotension: marked drop in blood pressure causing fainting or shock.

Precautions & Warnings

Before initiating therapy, consider the following precautions:

  • Monitor blood pressure: ensure adequate control and avoid excessive lowering.
  • Assess renal function: check serum creatinine and eGFR periodically.
  • Check electrolytes: especially potassium and sodium levels during treatment.
  • Use caution in hepatic impairment: dose adjustments may be needed.
  • Avoid in severe dehydration: rehydrate before starting the combination.
  • Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Olmesartan Medoxil + Hydrochlorothiazide may interact with several medicines.

Major Interactions (Avoid)

  • Aliskiren: combined use can cause excessive potassium elevation and renal impairment.
  • Potassium‑sparing diuretics (e.g., spironolactone): risk of hyperkalemia.
  • Lithium: increased lithium levels may lead to toxicity.
  • ACE inhibitors: additive effect on potassium and renal function.

Moderate Interactions (Monitor Closely)

  • Other antihypertensives: may cause additive blood‑pressure lowering.
  • Antidiabetic agents: diuretic‑induced changes in glucose may require dose adjustment.
  • CYP450 inhibitors (e.g., ketoconazole): may increase olmesartan plasma concentrations.

Frequently Asked Questions

Olmesartan Medoxil + Hydrochlorothiazide is an oral antihypertensive combination indicated for the treatment of primary (essential) hypertension. It lowers blood pressure by blocking angiotensin II receptors and promoting diuresis, helping to reduce cardiovascular risk in adult patients.

Olmesartan Medoxil is an angiotensin II receptor blocker (ARB). It selectively blocks AT1 receptors on blood‑vessel smooth muscle and adrenal glands, preventing angiotensin II‑induced vasoconstriction and aldosterone release, which leads to vasodilation and reduced blood‑pressure levels.

The dosage of Olmesartan Medoxil + Hydrochlorothiazide is individualized by the prescribing healthcare professional based on the patient’s blood‑pressure response, renal function, and other clinical factors. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

The safety of this combination during pregnancy or lactation has not been established. It is generally avoided in pregnant women because of potential fetal risk, and breastfeeding mothers should consult their physician before use.

To 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 (including any cold‑chain requirements) and necessary import documentation.

Compared with monotherapy ARBs or thiazide diuretics alone, the Olmesartan Medoxil + Hydrochlorothiazide combo offers synergistic blood‑pressure reduction, often achieving target levels more efficiently. It may be preferred when a single‑pill regimen is desired, but clinicians consider patient‑specific factors such as renal function and electrolyte balance when selecting therapy.

Store the tablets at room temperature, below 25 °C, in the original container to protect them from moisture and light. Keep out of reach of children and do not use if the packaging is damaged or the product appears discolored.

The medication is taken orally, usually once daily, with or without food, and swallowed whole with a glass of water. Patients should follow the dosing schedule prescribed by their healthcare provider and avoid crushing or chewing the tablet.

Serious risks include angioedema (swelling of the face, lips, tongue, or airway), severe dehydration, acute kidney injury, hyperkalemia, and marked hypotension. Any signs of these conditions require immediate medical attention.

The combination should be avoided in patients with known hypersensitivity to either component, severe renal impairment, severe hepatic disease, or in those who are markedly dehydrated. It is also contraindicated in individuals taking certain interacting medicines such as aliskiren or potassium‑sparing diuretics without close monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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