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

Olmesartan Medoxomilo + Hidroclorotiazida Ratiopharm

Active Ingredient:
Olmesartan Medoxomil, Hydrochlorothiazide
Origin:
EU

Olmesartan Medoxomilo + Hidroclorotiazida Ratiopharm (Olmesartan Medoxomil, Hydrochlorothiazide)

Olmesartan medoxomil, the active ingredient in Olmesartan Medoxomil + Hydrochlorothiazide Ratiopharm, is an angiotensin II receptor blocker presented as an oral tablet for oral use. It treats hypertension, often in combination with a thiazide diuretic, to lower blood pressure in adult patients.

GNH India supplies Olmesartan Medoxomil + Hydrochlorothiazide Ratiopharm as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company ensures quality compliance with EU standards and provides reliable logistics for global distribution.

Manufacturer / TM Owner

Ratiopharm-Comercio E Industria De Produtos Farmaceuticos Lda

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Indications & Clinical Uses

  • Olmesartan/HCTZ is used to manage hypertension by targeting the renin‑angiotensin system and promoting diuresis.
  • Essential hypertension: reduces elevated systolic and diastolic blood pressure.
  • Controlled hypertension: helps maintain target blood pressure levels.
  • Hypertension with fluid retention: combines vasodilation and diuretic action to improve blood pressure control.

How It Works

  • Olmesartan medoxomil selectively blocks angiotensin II type 1 (AT1) receptors, preventing vasoconstriction and aldosterone release, which lowers systemic vascular resistance. Hydrochlorothiazide acts on the distal convoluted tubule to inhibit Na⁺/Cl⁻ reabsorption, increasing urinary sodium and water excretion, thereby reducing plasma volume. The combined effect produces additive blood‑pressure reduction through decreased vascular tone and reduced fluid overload.

Side Effects

The combination may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Dizziness: light‑headed feeling, especially after standing.
  • Headache: mild to moderate pain.
  • Increased urination: more frequent bathroom visits.
  • Electrolyte imbalance (low potassium): mild muscle cramps.
  • Fatigue: general tiredness.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure causing fainting.
  • Acute kidney injury: sudden loss of renal function.
  • Hyperkalaemia: dangerously high potassium levels.
  • Allergic reaction: rash, swelling, or difficulty breathing.
  • Pancreatitis: severe abdominal pain.

Precautions & Warnings

Before prescribing, clinicians should consider several safety measures.

  • Monitor blood pressure: ensure adequate control and avoid excessive lowering.
  • Assess renal function: check serum creatinine and eGFR regularly.
  • Check electrolytes: especially potassium and sodium levels.
  • Avoid use in severe hepatic impairment: limited metabolism may increase exposure.
  • Use caution during pregnancy: potential fetal risk, evaluate benefit‑risk.
  • Store at room temperature: keep in original container, protect from moisture.

Avoid Interactions

Olmesartan/HCTZ can affect or be affected by other medicines, requiring attention to potential interactions.

Major Interactions (Avoid)

  • Aliskiren in diabetic patients: increased risk of renal dysfunction.
  • Potassium‑sparing diuretics (e.g., spironolactone): risk of hyperkalaemia.
  • ACE inhibitors or other ARBs: additive renal impairment.
  • NSAIDs (e.g., ibuprofen): may blunt antihypertensive effect.
  • Lithium: increased lithium toxicity.

Moderate Interactions (Monitor Closely)

  • Other thiazide diuretics: additive hypotension.
  • Beta‑blockers: enhanced blood‑pressure lowering.
  • CYP450 inhibitors (e.g., ketoconazole): may raise olmesartan levels.
  • Antacids containing aluminium or magnesium: reduce absorption.
  • Warfarin: monitor INR for possible changes.

Frequently Asked Questions

It is a prescription combination of an angiotensin‑II receptor blocker and a thiazide diuretic indicated for the treatment of hypertension in adults, helping lower blood pressure by reducing vascular resistance and fluid volume.

Olmesartan medoxomil selectively blocks AT1 receptors, preventing angiotensin II from causing vasoconstriction and aldosterone release, which leads to reduced systemic vascular resistance and lower blood pressure.

The dose is individualized by the prescribing clinician based on the patient’s blood‑pressure response, renal function, and concomitant therapies. The prescriber determines the appropriate tablet strength and dosing schedule.

Use during pregnancy is generally not recommended because angiotensin‑II receptor blockers may cause fetal toxicity. Safety in breastfeeding has not been established, so the benefits and risks should be carefully evaluated by a healthcare professional.

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 monotherapy ARBs or thiazides, the fixed‑dose combination offers additive blood‑pressure reduction, potentially improving adherence by reducing pill burden. It is an alternative to other ARB‑diuretic combos such as losartan‑hydrochlorothiazide, with a similar efficacy and safety profile.

Store the tablets at room temperature, below 25 °C, in the original blister pack or bottle. Protect from moisture and direct sunlight to maintain potency throughout the shelf life.

The tablets are taken orally, usually once daily, with or without food, as directed by the prescribing physician. 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, hyperkalaemia, and allergic reactions such as rash or swelling. Patients should seek immediate medical attention if they experience fainting, sudden loss of kidney function, facial or throat swelling, or difficulty breathing.

The combination is contraindicated in patients with known hypersensitivity to olmesartan, hydrochlorothiazide, or any component of the formulation, as well as those with severe renal impairment, anuria, or a history of angio‑edema related to ARB therapy. It should also be avoided in pregnancy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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