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

Olmesartan Medoxomil/Amlodipine/Hct Teva

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

Olmesartan Medoxomil/Amlodipine/Hct Teva (Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide)

Olmesartan medoxomil, the active ingredient in Olmesartan Medoxomil/Amlodipine/HCT Teva, is a combination antihypertensive presented as a tablet for oral use. It treats hypertension in adults by targeting the renin‑angiotensin system, calcium channels, and renal water‑salt balance.

GNH India supplies Olmesartan Medoxomil/Amlodipine/HCT Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Olmesartan Medoxomil/Amlodipine/HCT is a combination antihypertensive used to manage elevated blood pressure across several clinical presentations.

  • Essential hypertension: lowers both systolic and diastolic pressure in patients with primary hypertension.
  • Isolated systolic hypertension: provides arterial dilation and volume reduction to control high systolic readings.
  • Hypertension with fluid retention: adds diuretic effect to improve blood pressure control when edema is present.

How It Works

  • The combination works through three complementary mechanisms: olmesartan medoxomil blocks the angiotensin II type 1 receptor, preventing vasoconstriction and aldosterone release; amlodipine inhibits calcium influx into vascular smooth muscle, causing arterial dilation; and hydrochlorothiazide promotes renal excretion of sodium and water, reducing plasma volume. Together these actions produce a synergistic reduction in systemic blood pressure.

Side Effects

The following adverse reactions have been reported with the combination product.

Common Side Effects

  • Dizziness: sensation of light‑headedness, especially after standing.
  • Headache: mild to moderate pain often related to blood pressure changes.
  • Peripheral edema: swelling of the ankles or feet.
  • Fatigue: general feeling of tiredness.

Serious or Rare Side Effects

  • Angioedema: rapid swelling of face, lips, tongue, or throat requiring emergency care.
  • Severe hypotension: marked drop in blood pressure leading to fainting or shock.
  • Electrolyte imbalance: significant changes in potassium or sodium levels.
  • Renal impairment: worsening kidney function, especially in patients with pre‑existing disease.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety factors.

  • Renal function: monitor serum creatinine and potassium regularly.
  • Pregnancy: contraindicated (Category D) due to potential fetal harm.
  • Elderly patients: start at low dose and watch for orthostatic hypotension.
  • Concomitant potassium‑sparing agents: risk of hyperkalemia, requires monitoring.
  • Store at ambient temperature: keep in the original container, protect from moisture.

Avoid Interactions

Olmesartan Medoxomil/Amlodipine/HCT may interact with other medicines; some combinations should be avoided while others need close monitoring.

Major Interactions (Avoid)

  • Aliskiren (in diabetic patients): increased risk of renal failure.
  • Potassium supplements or ACE inhibitors: heightened risk of hyperkalemia.
  • Lithium: potential for elevated lithium concentrations.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may blunt antihypertensive effect.
  • Cyclosporine: can raise serum creatinine levels.
  • Beta‑blockers: additive hypotensive effect may require dose adjustment.

Frequently Asked Questions

Olmesartan Medoxomil/Amlodipine/HCT is a fixed‑dose combination tablet used to treat hypertension. It combines an angiotensin II receptor blocker, a calcium‑channel blocker, and a thiazide diuretic to lower blood pressure in adults with primary or secondary hypertension.

Olmesartan blocks the AT1 receptor, reducing vasoconstriction and aldosterone release. Amlodipine inhibits calcium entry into vascular smooth muscle, causing arterial dilation. Hydrochlorothiazide increases renal excretion of sodium and water, decreasing plasma volume. Together they provide complementary blood‑pressure‑lowering effects.

The specific dose and strength are determined by the prescribing clinician based on the patient’s blood‑pressure profile, age, renal function, and other medications. The prescriber will select the appropriate tablet strength and dosing schedule.

Olmesartan Medoxomil/Amlodipine/HCT is classified as Pregnancy Category D, indicating evidence of risk to the fetus. It is contraindicated in pregnancy and should be avoided. Safety during breastfeeding has not been established, so use is generally discouraged.

To place an order, 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 single‑agent therapy, the triple combination offers broader blood‑pressure control by targeting three mechanisms simultaneously, often allowing lower individual component doses and improving adherence. It may be preferred over separate tablets when multiple agents are needed, but clinicians consider patient‑specific factors and potential drug interactions.

Store the tablets at ambient temperature, preferably below 25 °C. Keep them in the original blister pack or container, protect from moisture and direct sunlight, and ensure the packaging remains tightly closed until use.

Olmesartan Medoxomil/Amlodipine/HCT is taken orally, usually once daily, with or without food, as directed by the prescriber. Swallow the tablet whole with a glass of water; do not crush or chew it.

Serious risks include angioedema, severe hypotension, significant electrolyte disturbances (especially low potassium), and acute kidney injury. Patients should be educated to seek immediate medical attention if they experience swelling of the face or throat, fainting, or rapid changes in urine output.

The combination is contraindicated in patients with known hypersensitivity to any component, in pregnant women, and in those with severe renal impairment or hyperkalemia. Caution is also advised for patients on potassium‑sparing diuretics or other agents that may increase potassium levels.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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