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

Idalazide

Active Ingredient:
Olmesartan Medoxomil, Hydrochlorothiazide
Origin:
EU

Idalazide (Olmesartan Medoxomil, Hydrochlorothiazide)

Olmesartan medoxomil, the active ingredient in Idalazide, is an Angiotensin II receptor blocker presented as an oral tablet for oral use. It is combined with hydrochlorothiazide, a thiazide diuretic, to treat hypertension in adult patients.

GNH India supplies Idalazide as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

I.B.N. Savio S.R.L.

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Indications & Clinical Uses

Idalazide is an antihypertensive medication that acts on the renin‑angiotensin system and promotes diuresis to lower blood pressure.

  • Hypertension: reduces systolic and diastolic blood pressure and helps prevent cardiovascular complications.
  • Essential high blood pressure: provides sustained control when monotherapy is insufficient.
  • Elevated arterial pressure: improves overall hemodynamic stability.

How It Works

  • Olmesartan medoxomil selectively blocks the AT1 receptor, preventing angiotensin II‑mediated vasoconstriction and aldosterone release. Hydrochlorothiazide inhibits NaCl reabsorption in the distal convoluted tubule, increasing urinary sodium and water excretion, which together lower peripheral resistance and plasma volume, resulting in reduced blood pressure.

Side Effects

Common Side Effects

  • Dizziness: transient light‑headedness, especially after the first dose.
  • Headache: mild to moderate intensity.
  • Fatigue: general tiredness without exertion.
  • Increased urination: due to the diuretic component.
  • Electrolyte imbalance: mild changes in potassium or sodium levels.
  • Cough: occasional dry throat irritation.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure causing fainting.
  • Acute kidney injury: sudden reduction in renal function.
  • Hyperkalemia: elevated potassium that may affect heart rhythm.
  • Angioedema: swelling of face, lips, or airway.
  • Pancreatitis: abdominal pain with elevated enzymes.
  • Liver dysfunction: abnormal liver enzyme elevations.

Precautions & Warnings

Before initiating Idalazide, consider the following precautions:

  • Blood pressure monitoring: ensure target levels are achieved without excessive drop.
  • Renal function assessment: evaluate serum creatinine and eGFR regularly.
  • Electrolyte surveillance: check potassium and sodium levels, especially with concomitant drugs.
  • Pregnancy safety: avoid use unless benefits outweigh potential risks, as safety data are limited.
  • Drug‑specific contraindications: do not use in patients with known hypersensitivity to either component.
  • Store at ambient temperature: keep below 25 °C in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Idalazide may interact with several medicines; awareness of these interactions helps maintain safety and efficacy.

Major Interactions (Avoid)

  • Aliskiren: combined use can cause severe hypotension and renal impairment.
  • Potassium‑sparing diuretics or supplements: risk of hyperkalemia.
  • Lithium: increased lithium levels may lead to toxicity.
  • ACE inhibitors or other ARBs: additive blood‑pressure lowering effect, may cause hypotension.
  • NSAIDs: can blunt antihypertensive effect and impair renal function.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may enhance blood‑pressure reduction.
  • Calcium channel blockers: additive hypotensive effect.
  • Antidiabetic agents: diuretic may affect glucose control.
  • Antimicrobials (e.g., trimethoprim): may increase risk of electrolyte disturbances.

Frequently Asked Questions

Idalazide is prescribed to lower high blood pressure in adults. It combines an angiotensin II receptor blocker with a thiazide diuretic to achieve better control of hypertension when a single agent is insufficient.

Olmesartan medoxomil blocks the AT1 receptors for angiotensin II, preventing vasoconstriction and aldosterone release. This leads to relaxed blood vessels and reduced fluid retention, contributing to lower blood pressure.

The specific dose of Idalazide is determined by the prescribing clinician based on the patient’s blood‑pressure profile, renal function, and other individual factors. Dosage adjustments are made according to therapeutic response and tolerability.

Safety data for Idalazide in pregnancy are limited, and the product is generally avoided unless the potential benefit justifies the risk. Breastfeeding mothers should consult their healthcare provider, as the drug may be excreted in milk.

To order Idalazide, 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.

Idalazide offers a dual mechanism—angiotensin II blockade plus diuresis—providing more potent blood‑pressure reduction than many single‑agent therapies. It is often chosen when monotherapy does not achieve target pressures, whereas alternatives may require separate prescriptions.

Idalazide tablets should be stored at ambient temperature, below 25 °C, in the original container. Protect them from moisture, excessive heat, and direct sunlight to maintain stability.

Idalazide is taken orally, usually once daily, with or without food, as directed by a healthcare professional. Swallow the tablet whole with a full glass of water.

Serious risks include severe hypotension, acute kidney injury, hyperkalemia, and angioedema. Patients should be monitored for signs such as dizziness, rapid weight loss, swelling of the face or throat, and changes in urine output.

Idalazide is contraindicated in individuals with known hypersensitivity to olmesartan, hydrochlorothiazide, or any component of the formulation. It should also be avoided in patients with severe renal impairment, hyperkalemia, or those taking interacting drugs that are contraindicated.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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