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

Olmesartan Medoxomilo + Hidroclorotiazida Alter

Active Ingredient:
Olmesartan Medoxomil, Hydrochlorothiazide
Origin:
EU

Olmesartan Medoxomilo + Hidroclorotiazida Alter (Olmesartan Medoxomil, Hydrochlorothiazide)

Olmesartan medoxil, the active ingredient in Olmesartan Medoxomilo + Hidroclorotiazida Alter, is an angiotensin II receptor blocker presented as a tablet for oral use. It treats hypertension, often in combination with a diuretic, and is prescribed for adults. GNH India supplies Olmesartan Medoxomilo + Hidroclorotiazida Alter as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

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

Manufacturer / TM Owner

Alter S.A.

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Indications & Clinical Uses

Olmesartan medoxil combined with hydrochlorothiazide acts on the renin‑angiotensin‑aldosterone system to lower blood pressure. Indicated indications include:

  • Hypertension: improves blood pressure control when monotherapy is insufficient.
  • Hypertensive urgency: assists in achieving target pressures more rapidly under medical supervision.
  • Diastolic heart failure with fluid overload: reduces preload and afterload, aiding symptom management.
  • Chronic kidney disease with hypertension: slows progression by controlling systemic pressure.
  • Post‑myocardial infarction hypertension: helps maintain optimal hemodynamics after an event.

How It Works

  • Olmesartan medoxil selectively blocks the angiotensin II type 1 (AT1) receptor, preventing angiotensin II‑mediated vasoconstriction, aldosterone release, and sympathetic activation. Hydrochlorothiazide inhibits sodium‑chloride reabsorption in the distal convoluted tubule, promoting natriuresis and diuresis, which together lower intravascular volume and systemic vascular resistance, resulting in reduced blood pressure.

Side Effects

Olmesartan medoxil with hydrochlorothiazide may cause a range of adverse reactions.

Common Side Effects

  • Dizziness: light‑headed sensation, especially after standing.
  • Headache: mild to moderate intensity.
  • Fatigue: general feeling of tiredness.
  • Electrolyte imbalance: low potassium or sodium levels.
  • Increased urination: due to the diuretic component.
  • Mild gastrointestinal discomfort: nausea or abdominal pain.

Serious or Rare Side Effects

  • Severe hypotension: markedly low blood pressure requiring medical attention.
  • Acute kidney injury: sudden decline in renal function.
  • Hyperkalemia: elevated potassium levels, potentially life‑threatening.
  • Angioedema: swelling of face, lips, tongue, or airway.
  • Liver enzyme elevation: signs of hepatic stress.
  • Blood dyscrasias: rare blood cell abnormalities.

Precautions & Warnings

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

  • Renal function: assess baseline creatinine and eGFR, adjust if impaired.
  • Electrolytes: check serum potassium and sodium before and during treatment.
  • Pregnancy: avoid use; teratogenic risk is documented for ARBs.
  • Concomitant drugs: review for additive potassium‑sparing or diuretic effects.
  • Elderly patients: start with lower dose and monitor for orthostatic changes.
  • Store at below 25°C: keep in the original container, protect from moisture and light.

Avoid Interactions

Olmesartan medoxil with hydrochlorothiazide can interact with several drug classes, requiring clinical awareness.

Major Interactions (Avoid)

  • Aliskiren: combined use in diabetes or renal impairment may increase risk of renal dysfunction.
  • Potassium‑sparing diuretics or supplements: may cause dangerous hyper‑kalemia.
  • NSAIDs: can blunt antihypertensive effect and worsen renal function.

Moderate Interactions (Monitor Closely)

  • Lithium: may increase lithium levels, risking toxicity.
  • Antidiabetic agents: enhanced glucose‑lowering effect may require dose adjustment.
  • ACE inhibitors or other ARBs: additive blood pressure lowering and renal risk.
  • Loop diuretics: may intensify volume depletion and electrolyte disturbances.
  • Antidepressants (SSRIs): modest increase in hyponatremia risk.

Frequently Asked Questions

Olmesartan Medoxomilo + Hidroclorotiazida Alter is a fixed‑dose combination of an angiotensin II receptor blocker and a thiazide diuretic. It is prescribed to lower high blood pressure in adults, especially when monotherapy does not achieve target levels, and to reduce fluid retention associated with hypertension.

Olmesartan medoxil blocks the AT1 receptor for angiotensin II, preventing vasoconstriction and aldosterone release. Hydrochlorothiazide acts on the distal convoluted tubule to inhibit sodium‑chloride reabsorption, increasing urine output. Together they lower vascular resistance and circulating volume, producing an overall antihypertensive effect.

The dose is individualized by the prescribing clinician based on the patient’s blood pressure, renal function, and response to therapy. Physicians select the appropriate strength and titrate as needed, following local prescribing guidelines.

Olmesartan medoxil is classified as contraindicated in pregnancy because ARBs can cause fetal toxicity. It is also not recommended while breastfeeding, as the drug may pass into milk and affect the infant. Alternative antihypertensives are preferred for pregnant or lactating patients.

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 necessary import documentation.

Compared with single‑agent ARBs, the addition of hydrochlorothiazide offers enhanced blood‑pressure reduction and addresses fluid overload. It can be more convenient than prescribing two separate pills, but the combination may increase the risk of electrolyte disturbances versus monotherapy. Choice depends on individual patient profile and treatment goals.

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

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

Serious risks include severe hypotension, acute kidney injury, hyperkalemia, and angioedema. Patients should be monitored for sudden drops in blood pressure, changes in renal function, swelling of the face or throat, and abnormal electrolyte levels.

Contraindications include known hypersensitivity to olmesartan, hydrochlorothiazide, or any component of the formulation, pregnancy, severe renal impairment, and patients with hyperkalemia or anuria. Clinicians should also avoid use in individuals taking other potassium‑sparing agents without careful monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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