Product image of Olmesartán/Hidroclorotiazida Combix (Olmesartan Medoxomil, Hydrochlorothiazide) supplied by GNH India

Olmesartán/Hidroclorotiazida Combix

Active Ingredient:
Olmesartan Medoxomil, Hydrochlorothiazide
Origin:
EU

Olmesartán/Hidroclorotiazida Combix (Olmesartan Medoxomil, Hydrochlorothiazide)

Olmesartan Medoxomil, the active ingredient in Olmesartán/Hidroclorotiazida Combix, is a angiotensin II receptor blocker presented as a combination tablet for oral use. It treats hypertension, often in combination with a thiazide diuretic, and is intended for adult patients. GNH India supplies Olmesartán/Hidroclorotiazida Combix as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

GNH India supplies Olmesartán/Hidroclorotiazida Combix as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Laboratorios Combix, S.L.U.

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Indications & Clinical Uses

Olmesartan Medoxomil/Hydrochlorothiazide is used in the management of high blood pressure through combined renin‑angiotensin blockade and diuresis.

  • Hypertension: improves blood pressure control when monotherapy is insufficient.
  • Heart failure with reduced ejection fraction: assists in volume management and afterload reduction as part of guideline‑directed therapy.
  • Diabetic nephropathy: helps slow progression of renal impairment by lowering systemic pressure.
  • Post‑myocardial infarction hypertension: supports secondary prevention by maintaining target pressures.
  • Chronic kidney disease stage 3–4: contributes to proteinuria reduction and pressure control.
  • Resistant hypertension: provides an additional mechanism when other agents have failed.

How It Works

  • Olmesartan Medoxomil selectively blocks the angiotensin II type 1 (AT1) receptor, preventing vasoconstriction and aldosterone release. Hydrochlorothiazide inhibits sodium‑chloride reabsorption in the distal convoluted tubule, promoting natriuresis and diuresis. The combination yields additive blood‑pressure reduction by decreasing peripheral resistance and plasma volume.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Dizziness or light‑headedness
  • Headache
  • Fatigue
  • Increased urination
  • Electrolyte disturbances (e.g., low potassium)
  • Mild gastrointestinal discomfort

Serious or Rare Side Effects

  • Severe hypotension
  • Acute kidney injury
  • Hyperkalemia or severe electrolyte imbalance
  • Angio‑edema
  • Liver function abnormalities
  • Blood dyscrasias such as agranulocytosis

Precautions & Warnings

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

  • Renal function: assess baseline creatinine and eGFR, adjust if impaired.
  • Electrolytes: monitor potassium and sodium levels regularly.
  • Pregnancy: contraindicated in the second and third trimesters; avoid unless benefits outweigh risks.
  • Concomitant drugs: review for potential additive potassium‑sparing effects.
  • Gout: use cautiously in patients with a history of hyperuricemia.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Olmesartan/Hydrochlorothiazide may interact with several drug classes; monitoring is advised.

Major Interactions (Avoid)

  • Aliskiren (combined renin‑angiotensin inhibition may cause renal impairment).
  • Potassium‑sparing diuretics or supplements (risk of hyperkalemia).
  • Lithium (increased lithium levels and toxicity).

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) (may reduce antihypertensive effect and affect renal function).
  • ACE inhibitors or other ARBs (additive hypotensive effect).
  • Antidiabetic agents (enhanced glucose‑lowering effect, risk of hypoglycaemia).

Frequently Asked Questions

Olmesartán/Hidroclorotiazida Combix is a fixed‑dose combination of olmesartan medoxomil and hydrochlorothiazide indicated for the treatment of hypertension, often when monotherapy does not achieve target blood‑pressure levels. It may also be used as part of broader cardiovascular risk‑reduction strategies in adults.

Olmesartan medoxomil is an angiotensin II receptor blocker that selectively inhibits the AT‑1 receptor, preventing angiotensin‑II‑mediated vasoconstriction and aldosterone secretion. This results in relaxed blood vessels and reduced sodium‑water retention, lowering systemic blood pressure.

The specific dose of Olmesartán/Hidroclorotiazida Combix is determined by the prescribing clinician based on the patient’s blood‑pressure readings, renal function, and overall treatment plan. Dosage adjustments are made according to clinical response and tolerability.

Olmesartan is contraindicated in the second and third trimesters of pregnancy because of the risk of fetal toxicity. Use during breastfeeding is not recommended unless the benefit outweighs potential risk, and the decision should be made by a healthcare professional.

To place an order, submit an enquiry on the product page at gnhindia.com, providing the required quantity and your institutional credentials. GNH India works with hospitals, pharmacies and procurement teams worldwide, then replies with pricing, availability, shipping details and any necessary import documentation.

Compared with single‑agent therapy, the olmesartan/hydrochlorothiazide combo offers dual mechanisms—angiotensin‑II blockade and diuresis—providing greater blood‑pressure reduction in many patients. It can be more convenient than taking two separate pills and may improve adherence, while safety profiles are similar to each component used alone.

Store the tablets at temperatures below 25 °C in their original container, protecting them from moisture, heat and direct sunlight. Do not use the product after the expiry date printed on the packaging.

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

Serious adverse events can include severe hypotension, acute kidney injury, hyperkalemia, angio‑edema and liver function abnormalities. Patients should seek immediate medical attention if they experience symptoms such as swelling of the face or throat, rapid weight loss, or marked dizziness.

The combination should be avoided in patients with known hypersensitivity to olmesartan, hydrochlorothiazide or any excipients, in those with severe renal impairment, hyperkalemia, or in pregnant women during the second and third trimesters. Clinicians must assess individual risk before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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