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

Olmeamlo Hct

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

Olmeamlo Hct (Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide)

Olmesartan medoxomil, amlodipine, hydrochlorothiazide, the active ingredient in Olmeamlo Hct, is a combination antihypertensive presented as a tablet for oral use. It treats hypertension in adults, often when single‑agent therapy does not provide adequate blood pressure control.

GNH India supplies Olmeamlo Hct as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Tad Pharma Gmbh

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Indications & Clinical Uses

Olmeamlo Hct is indicated for hypertension, a condition characterized by elevated arterial pressure, and works within the cardiovascular system to lower blood pressure.

  • Hypertension: helps achieve target blood pressure levels and reduces cardiovascular risk.
  • Hypertension resistant to monotherapy: provides additional blood pressure reduction when a single agent is insufficient.
  • Hypertension with fluid retention: combines a diuretic to address volume overload while lowering pressure.

How It Works

  • The combination product lowers blood pressure through three complementary mechanisms: olmesartan medoxomil blocks the angiotensin II type 1 receptor, preventing vasoconstriction; amlodipine inhibits calcium influx into vascular smooth‑muscle cells, causing arterial dilation; and hydrochlorothiazide promotes renal excretion of sodium and water, decreasing plasma volume. Together these actions produce additive antihypertensive effects.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Headache: mild to moderate headache.
  • Peripheral edema: swelling of the ankles or feet.
  • Dizziness or light‑headedness: especially after standing.
  • Flushing: transient warmth and redness.
  • Fatigue: general tiredness.
  • Nausea: mild stomach upset.

Serious or Rare Side Effects

  • Angio‑edema: rapid swelling of face, lips or throat.
  • Severe hypotension: marked drop in blood pressure causing fainting.
  • Electrolyte imbalance: significant changes in potassium or sodium levels.
  • Acute kidney injury: sudden decline in renal function.
  • Hepatic dysfunction: abnormal liver enzyme elevations.
  • Severe skin reactions: such as Stevens‑Johnson syndrome.

Precautions & Warnings

Before initiating therapy, consider the following safety measures:

  • Renal function: assess baseline kidney function and monitor periodically.
  • Electrolytes: check serum potassium and sodium levels, especially with diuretic use.
  • Cardiovascular status: evaluate for heart failure or recent myocardial infarction.
  • Pregnancy and lactation: avoid use unless clearly needed; discuss risks with a healthcare professional.
  • Drug hypersensitivity: review patient history for allergies to any component.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Olmeamlo Hct may interact with several drug classes; monitoring and dose adjustments are often required.

Major Interactions (Avoid)

  • Aliskiren: concurrent use with ACE inhibitors or ARBs can increase risk of renal impairment.
  • Potassium‑saving diuretics or supplements: may cause hyperkalaemia.
  • 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.
  • CYP3A4 inhibitors (e.g., erythromycin, clarithromycin): can raise amlodipine concentrations.
  • Antidiabetic agents: may enhance glucose‑lowering effect, requiring dose adjustment.

Frequently Asked Questions

Olmeamlo Hct is a fixed‑dose combination tablet that contains olmesartan medoxomil, amlodipine and hydrochlorothiazide. It is prescribed to lower high blood pressure in adults, especially when a single antihypertensive agent does not achieve target levels or when fluid retention is present.

Olmesartan medoxomil blocks angiotensin II receptors, preventing vasoconstriction; amlodipine relaxes vascular smooth muscle by inhibiting calcium entry, leading to arterial dilation; and hydrochlorothiazide increases urinary excretion of sodium and water, reducing blood volume. The three mechanisms act together to lower systemic blood pressure.

The dose of Olmeamlo Hct is individualized by the prescribing clinician based on the patient’s blood pressure, response to therapy and tolerability. The prescriber determines the appropriate strength and dosing schedule.

Olmesartan medoxomil is classified as contraindicated in pregnancy because it can harm the developing fetus. Amlodipine and hydrochlorothiazide are also not recommended unless the benefit outweighs risk. Breastfeeding mothers should consult their healthcare provider before using this combination.

To place an order, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details and any necessary import documentation.

Olmeamlo Hct combines an angiotensin‑II receptor blocker, a calcium‑channel blocker and a thiazide diuretic in one tablet, offering broader blood‑pressure reduction than single‑agent therapy. Compared with separate tablets, it may improve adherence but requires careful monitoring for additive side‑effects.

Store Olmeamlo Hct tablets at temperatures below 25 °C in their original container, protected from moisture and direct sunlight. Do not freeze or expose the product to excessive heat.

Olmeamlo Hct is taken orally, usually once daily, with or without food as directed by the prescribing clinician. Swallow the tablet whole with a glass of water; do not crush or chew unless specifically instructed.

Serious risks include angio‑edema, severe hypotension, electrolyte disturbances (especially low potassium or sodium), acute kidney injury and rare severe skin reactions. Patients should seek immediate medical attention if they experience swelling of the face or throat, fainting, or unusual skin rashes.

Individuals with known hypersensitivity to any component, pregnant women, patients with severe renal impairment, or those taking contraindicated medications such as aliskiren in combination with an ARB should avoid this product unless a healthcare professional determines it is appropriate.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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