Product image of Olmesartan/Hidroclorotiazida Kern Pharma (Olmesartan Medoxomil, Hydrochlorothiazide) supplied by GNH India

Olmesartan/Hidroclorotiazida Kern Pharma

Active Ingredient:
Olmesartan Medoxomil, Hydrochlorothiazide
Origin:
EU

Olmesartan/Hidroclorotiazida Kern Pharma (Olmesartan Medoxomil, Hydrochlorothiazide)

Olmesartan medoxomil, the active ingredient in Olmesartan/Hidroclorotiazida Kern Pharma, is an angiotensin II receptor blocker presented as an oral tablet for oral use. It is combined with hydrochlorothiazide to treat hypertension in adult patients.

GNH India supplies Olmesartan/Hidroclorotiazida Kern Pharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Kern Pharma, S.L.

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Indications & Clinical Uses

Olmesartan/Hidroclorotiazida is an antihypertensive combination that lowers elevated blood pressure in patients with primary hypertension.

  • Hypertension: reduces systolic and diastolic blood pressure and helps prevent cardiovascular complications associated with uncontrolled hypertension.

How It Works

  • Olmesartan medoxomil selectively blocks AT1 receptors, preventing angiotensin II‑mediated vasoconstriction and aldosterone release. Hydrochlorothiazide inhibits the Na⁺/Cl⁻ symporter in the distal convoluted tubule, promoting sodium and water excretion. The dual action results in decreased peripheral vascular resistance and reduced plasma volume, producing an overall antihypertensive effect.

Side Effects

Common Side Effects

  • Dizziness: feeling light‑headed or unsteady.
  • Headache: mild to moderate head pain.
  • Fatigue: unusual tiredness or lack of energy.
  • Increased urination: more frequent need to void.
  • Electrolyte imbalance: changes in potassium or sodium levels.
  • Dry mouth: reduced salivation.

Serious or Rare Side Effects

  • Severe hypotension: dangerously low blood pressure.
  • Acute kidney injury: sudden decline in renal function.
  • Hyperkalemia: elevated potassium levels.
  • Allergic reactions: rash, itching, swelling, or anaphylaxis.
  • Pancreatitis: inflammation of the pancreas.
  • Blood dyscrasias: abnormal blood cell counts.

Precautions & Warnings

Before initiating therapy, consider the following precautions:

  • Blood pressure monitoring: ensure adequate control and avoid excessive drops.
  • Renal function assessment: evaluate creatinine and eGFR, especially in patients with pre‑existing kidney disease.
  • Electrolyte surveillance: check potassium and sodium levels regularly.
  • Hepatic impairment: use with caution in severe liver disease.
  • Diabetes mellitus: monitor glucose as diuretics may affect glycaemic control.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Olmesartan/Hidroclorotiazida may interact with several medicines.

Major Interactions (Avoid)

  • Aliskiren: combined use can cause excessive potassium rise and renal dysfunction.
  • ACE inhibitors or other ARBs: additive hypotensive effect and risk of hyperkalemia.
  • Lithium: increased lithium levels leading to toxicity.
  • Potassium‑sparing diuretics or supplements: risk of severe hyperkalemia.
  • NSAIDs (high dose): may blunt antihypertensive effect and impair renal function.

Moderate Interactions (Monitor Closely)

  • Other antihypertensives: may require dose adjustment to prevent hypotension.
  • Loop diuretics: combined diuretic effect can cause volume depletion.
  • CYP450 inhibitors (e.g., fluconazole): may modestly increase olmesartan levels.

Frequently Asked Questions

Olmesartan/Hidroclorotiazida is prescribed to lower high blood pressure in adults with primary (essential) hypertension. The combination of an angiotensin II receptor blocker and a thiazide diuretic provides complementary mechanisms to achieve better blood‑pressure control and reduce the risk of cardiovascular events.

Olmesartan medoxomil blocks AT1 receptors, preventing angiotensin II from causing vasoconstriction and stimulating aldosterone release. This leads to relaxed blood vessels and reduced fluid retention, which together lower systemic blood pressure.

The exact dose is determined by the prescribing clinician based on the patient’s blood‑pressure readings, renal function, and other individual factors. The prescriber will select the appropriate strength and dosing schedule according to clinical guidelines.

Safety in pregnancy and lactation has not been established for this combination. It is generally avoided in pregnant women because angiotensin‑II receptor blockers may harm the fetus. Breastfeeding mothers should consult their healthcare provider before use.

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

Compared with single‑agent ARBs or thiazide diuretics, the Olmesartan/Hidroclorotiazida combo offers dual mechanisms that often achieve better blood‑pressure reduction at lower individual doses, potentially improving adherence. However, the combination may carry a higher risk of electrolyte disturbances than monotherapy, requiring regular monitoring.

Store the tablets at room temperature, below 25 °C, in the original blister pack or container. Keep them away from moisture, heat and direct sunlight 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 adverse events include severe hypotension, acute kidney injury, hyperkalemia, and allergic reactions such as rash or anaphylaxis. Patients should seek immediate medical attention if they experience faintness, rapid weight gain, swelling, difficulty breathing, or signs of infection.

The combination is contraindicated in patients with known hypersensitivity to olmesartan, hydrochlorothiazide, or any component of the formulation, as well as in those with severe renal impairment, hyperkalemia, or anuria. Caution is also advised for individuals with severe liver disease or electrolyte disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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