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

Olimesta Combi

Active Ingredient:
Olmesartan Medoxomil, Hydrochlorothiazide
Origin:
EU

Olimesta Combi (Olmesartan Medoxomil, Hydrochlorothiazide)

Olmesartan medoxomil, the active ingredient in Olimesta Combi, is an angiotensin II receptor blocker presented as a fixed‑dose combination tablet for oral use. It treats hypertension, often in combination with a diuretic, and is intended for adult patients requiring blood‑pressure control.
GNH India supplies Olimesta Combi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Krka Sverige Ab

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Indications & Clinical Uses

Olimesta Combi combines two antihypertensive agents that act on the renin‑angiotensin‑aldosterone system to lower blood pressure.

  • Hypertension: provides effective blood‑pressure reduction in patients who need combined ARB and thiazide therapy.
  • Resistant hypertension: adds diuretic effect to improve control when monotherapy is insufficient.
  • Edema associated with hypertension: helps reduce fluid retention through the diuretic component.

How It Works

  • Olmesartan medoxomil blocks the binding of angiotensin II to the AT1 receptor on vascular smooth‑muscle and adrenal cells, preventing vasoconstriction and aldosterone release. Hydrochlorothiazide inhibits sodium‑chloride reabsorption in the distal convoluted tubule, promoting diuresis and further lowering circulating volume and peripheral resistance.

Side Effects

Adverse reactions may range from mild to serious and should be monitored during therapy.

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
  • Angio‑edema
  • Severe electrolyte imbalance
  • Allergic skin reactions (e.g., Stevens‑Johnson syndrome)

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: monitor potassium and sodium levels regularly.
  • Pregnancy: contraindicated in the second and third trimesters; avoid use.
  • Concomitant drugs: review for potential interactions, especially other antihypertensives.
  • Orthostatic hypotension: advise patients to rise slowly to reduce fall risk.
  • Store below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Olimesta Combi may interact with several drug classes; careful review is essential.

Major Interactions (Avoid)

  • Aliskiren (in diabetic patients): risk of renal dysfunction and hyperkalemia.
  • Potassium‑sparing diuretics or supplements: may cause dangerous hyperkalemia.
  • Lithium: increased lithium levels and toxicity risk.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may blunt antihypertensive effect and affect renal function.
  • ACE inhibitors or other ARBs: additive blood‑pressure lowering, risk of hypotension.
  • Antidiabetic agents: may enhance glucose‑lowering effect, requiring dose adjustment.

Frequently Asked Questions

Olimesta Combi is a fixed‑dose combination of olmesartan medoxomil and hydrochlorothiazide indicated for the treatment of hypertension in adults, including cases where a single‑agent regimen does not provide adequate blood‑pressure control.

Olmesartan medoxomil is an angiotensin II receptor blocker that selectively inhibits the AT1 receptor, preventing angiotensin II‑mediated vasoconstriction and aldosterone release, which helps to relax blood vessels and lower blood pressure.

The appropriate dose of Olimesta Combi is determined by the prescribing clinician based on the patient’s blood‑pressure readings, renal function and overall health status. Dosage adjustments are made according to therapeutic response and tolerability.

Olmesartan‑containing products are contraindicated in pregnancy, especially after the first trimester, because of the risk of fetal toxicity. Limited data exist for breastfeeding, and the drug is generally avoided unless the benefit outweighs potential risk.

To place an order, submit an enquiry on the Olimesta Combi product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies institutional credentials, and then provides pricing, availability, shipping details and import documentation.

Compared with monotherapy ARBs or thiazide diuretics, Olimesta Combi offers combined blood‑pressure reduction in a single tablet, which can improve adherence. It provides similar efficacy to other ARB‑thiazide combinations but differs in pharmacokinetic profile and specific dosing strengths.

Store the tablets below 25 °C in their original container, protecting them from moisture, heat and direct sunlight to maintain potency throughout the shelf‑life.

Olimesta Combi is taken orally, usually once daily, with or without food, as directed by a healthcare professional. Swallow the tablet whole; do not crush or chew it.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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