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

Olmesartán/Amlodipino/Hidroclorotiazida Normon

Active Ingredient:
Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide
Origin:
EU

Olmesartán/Amlodipino/Hidroclorotiazida Normon (Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide)

Olmesartan medoxil, the active ingredient in Olmesartán/Amlodipino/Hidroclorotiazida Normon, is a combination antihypertensive presented as a tablet for oral use. It treats high blood pressure in adults, often when single‑component therapy is insufficient. GNH India supplies Olmesartán/Amlodipino/Hidroclorotiazida Normon as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

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

Manufacturer / TM Owner

Laboratorios Normon, S.A.

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Indications & Clinical Uses

Olmesartan/Amlodipine/Hydrochlorothiazide is used in the management of hypertension, acting on multiple pathways that control blood pressure.

  • Essential hypertension: lowers systolic and diastolic pressure to reduce cardiovascular risk.
  • Hypertension with edema: combines vasodilation and diuresis to improve fluid balance.
  • Hypertension in patients requiring multiple mechanisms: provides angiotensin‑II blockade, calcium‑channel blockade and thiazide‑type diuresis in one tablet.

How It Works

  • The combination product pairs an angiotensin‑II receptor blocker (olmesartan) that inhibits vasoconstriction, a calcium‑channel blocker (amlodipine) that relaxes vascular smooth muscle, and a thiazide‑type diuretic (hydrochlorothiazide) that reduces plasma volume, together producing additive blood‑pressure‑lowering effects.

Side Effects

Side effects may occur with any antihypertensive regimen and should be monitored during therapy.

Common Side Effects

  • Dizziness or light‑headedness
  • Headache
  • Peripheral edema
  • Flushing
  • Fatigue
  • Increased urination

Serious or Rare Side Effects

  • Severe hypotension
  • Acute kidney injury
  • Electrolyte disturbances (e.g., low potassium)
  • Angio‑edema
  • Liver function abnormalities
  • Severe skin reactions such as Stevens‑Johnson syndrome

Precautions & Warnings

Before prescribing this combination, clinicians should assess patient history and monitor relevant parameters.

  • Renal function: evaluate creatinine and eGFR before initiation and periodically thereafter.
  • Electrolytes: check serum potassium and sodium levels, especially when using other diuretics.
  • Cardiovascular status: monitor for symptomatic hypotension after the first dose.
  • Pregnancy: contraindicated in the second and third trimesters; avoid use.
  • Drug hypersensitivity: discontinue if angio‑edema or severe rash develops.
  • Store at ambient temperature: keep tablets in the original container, protect from moisture and light.

Avoid Interactions

Olmesartan/Amlodipine/Hydrochlorothiazide may interact with several drug classes; clinicians should review patient medication lists.

Major Interactions (Avoid)

  • Aliskiren (in diabetic patients): risk of renal impairment and hyperkalemia.
  • Potassium‑sparing diuretics or supplements: may cause dangerous hyperkalemia.
  • NSAIDs (high‑dose or chronic): can blunt antihypertensive effect and impair renal function.

Moderate Interactions (Monitor Closely)

  • Lithium: may increase lithium levels, risking toxicity.
  • CYP3A4 inhibitors (e.g., itraconazole, clarithromycin): can raise amlodipine concentrations.
  • Antidiabetic agents: may require dose adjustment due to enhanced glucose‑lowering effect.

Frequently Asked Questions

Olmesartán/Amlodipino/Hidroclorotiazida Normon is a fixed‑dose combination tablet that treats high blood pressure. It is prescribed for adults with essential hypertension, especially when blood pressure is not adequately controlled with a single‑component drug, and it helps reduce the risk of cardiovascular events associated with sustained hypertension.

Olmesartan is an angiotensin‑II receptor blocker that selectively blocks the AT‑1 receptor, preventing angiotensin‑II‑mediated vasoconstriction and aldosterone release. This results in relaxed blood vessels and reduced sodium‑water retention, contributing to lower blood pressure when combined with the other two agents.

The specific dose of this combination tablet is determined by the prescribing clinician based on the patient’s blood‑pressure level, response to therapy, and overall health profile. Physicians adjust the dose to achieve target blood‑pressure goals while monitoring safety.

Use of this combination is contraindicated during the second and third trimesters of pregnancy because of potential harm to the fetus. It should be used only if clearly needed in the first trimester. Breastfeeding mothers should consult a healthcare professional, as the drugs may pass into breast milk.

To place an order, visit the product page on gnhindia.com, submit an enquiry with the required quantity, and provide institutional or trade credentials. GNH India works with hospitals, pharmacies and procurement teams worldwide, responding with pricing, availability, shipping details and any necessary import documentation.

Compared with single‑agent therapy, this triple‑component tablet offers convenience and synergistic blood‑pressure reduction by targeting three mechanisms: angiotensin‑II blockade, calcium‑channel mediated vasodilation, and thiazide‑type diuresis. It can simplify regimens and improve adherence versus taking three separate pills, while providing comparable efficacy to other combination products.

Store the tablets at ambient temperature, below 25 °C, in the original packaging to protect them from moisture and light. Keep the container tightly closed and out of reach of children.

The medication is taken orally, usually once daily, with or without food, as directed by the prescribing clinician. Patients should swallow the tablet whole with a glass of water and follow any specific timing instructions provided by their healthcare provider.

Serious risks include severe hypotension, acute kidney injury, significant electrolyte imbalances such as hyper‑kalemia, and rare cases of angio‑edema. Patients should seek immediate medical attention if they experience swelling of the face or throat, sudden dizziness, or marked changes in urine output.

The combination should be avoided in patients with known hypersensitivity to any component, those with severe renal impairment, pregnant women in the second or third trimester, and individuals with a history of angio‑edema related to angiotensin‑II receptor blockers.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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