Product image of Olmesartan Medoxomil/Amlodipine/Hydrochlorothiazide Alembic (Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide) supplied by GNH India

Olmesartan Medoxomil/Amlodipine/Hydrochlorothiazide Alembic

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

Olmesartan Medoxomil/Amlodipine/Hydrochlorothiazide Alembic (Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide)

Olmesartan medoxil, the active ingredient in Olmesartan Medoxil/Amlodipine/Hydrochlorothiazide Alembic, is an angiotensin II receptor blocker (ARB) presented as a tablet for oral use. It is combined with amlodipine and hydrochlorothiazide to treat hypertension in adult patients.

GNH India supplies Olmesartan Medoxil/Amlodipine/Hydrochlorothiazide Alembic as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Alembic Pharmaceuticals Europe Ltd

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Indications & Clinical Uses

Olmesartan Medoxil/Amlodipine/Hydrochlorothiazide is indicated for hypertension, acting on the renin‑angiotensin system and vascular smooth muscle.

  • Essential hypertension: reduces systolic and diastolic blood pressure.
  • Hypertension with fluid retention: adds diuretic effect to improve control.
  • Hypertension requiring multiple mechanisms: provides combined ARB, calcium‑channel blockade, and diuresis for better efficacy.

How It Works

  • Olmesartan medoxil selectively blocks angiotensin II type‑1 (AT1) receptors, preventing vasoconstriction and aldosterone release. Amlodipine inhibits calcium influx into vascular smooth‑muscle cells, causing arterial dilation. Hydrochlorothiazide promotes sodium and water excretion by inhibiting Na⁺/Cl⁻ reabsorption in the distal convoluted tubule. Together these actions lower peripheral resistance, reduce plasma volume, and achieve synergistic blood‑pressure control.

Side Effects

Common Side Effects

  • Dizziness
  • Headache
  • Peripheral edema
  • Flushing
  • Cough
  • Fatigue

Serious or Rare Side Effects

  • Angioedema
  • Severe hypotension
  • Electrolyte imbalance (e.g., hyper‑ or hypokalemia)
  • Acute renal impairment
  • Hepatic dysfunction
  • Pancreatitis

Precautions & Warnings

Before initiating therapy, consider the following precautions:

  • Renal function: monitor serum creatinine and potassium levels.
  • Electrolytes: check for hypokalemia or hyperkalemia, especially with diuretic use.
  • Pregnancy: contraindicated in the second and third trimesters.
  • Elderly patients: start at lower dose and monitor for orthostatic hypotension.
  • Concomitant drugs: avoid NSAIDs that may blunt antihypertensive effect.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Olmesartan Medoxil/Amlodipine/Hydrochlorothiazide may interact with other medicines as follows:

Major Interactions (Avoid)

  • Potassium‑sparing diuretics: risk of hyperkalemia.
  • ACE inhibitors or aliskiren in diabetic patients: increased risk of renal dysfunction.
  • NSAIDs: may reduce antihypertensive efficacy.
  • Lithium: increased lithium toxicity.
  • Concomitant use with other ARBs: additive renal effects.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., ketoconazole): may raise amlodipine levels.
  • CYP3A4 inducers (e.g., rifampicin): may lower amlodipine exposure.
  • Antacids containing aluminum or magnesium: may affect absorption.
  • Beta‑blockers: additive hypotensive effect.
  • Antidiabetic agents: may require dose adjustment due to improved glycemic control.

Frequently Asked Questions

It is a fixed‑dose combination indicated for the treatment of hypertension in adults, providing blood‑pressure reduction through three complementary mechanisms: AT1‑receptor blockade, calcium‑channel inhibition, and thiazide‑type diuresis.

Olmesartan medoxil selectively blocks the angiotensin II type‑1 (AT1) receptor, preventing vasoconstriction and aldosterone release, which lowers peripheral vascular resistance and reduces blood‑volume retention.

The prescribed dose is determined by the treating physician based on the patient’s blood‑pressure response, renal function, and concomitant therapies; dosing is individualized and not standardized in public literature.

Use is contraindicated during the second and third trimesters of pregnancy because of potential fetal toxicity. Safety during breastfeeding has not been established, so a risk‑benefit assessment is required before use.

Submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India verifies institutional credentials, then provides pricing, availability, shipping details, and any necessary import documentation.

Compared with monotherapy, the triple‑component tablet offers broader blood‑pressure control by simultaneously targeting the renin‑angiotensin system, calcium channels, and renal sodium‑water balance, often reducing the need for multiple separate pills.

Store at ambient temperature below 25 °C in the original blister pack, protect from moisture and direct sunlight, and keep out of reach of children.

The tablet 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.

Serious adverse events include angioedema, severe hypotension, electrolyte disturbances such as hyper‑ or hypokalemia, and acute kidney injury. Immediate medical attention is required if any of these occur.

Individuals with known hypersensitivity to any component, severe renal impairment, hepatic failure, or those who are pregnant beyond the first trimester should avoid this product. Clinicians must assess suitability before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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