Product image of Olmedipin Plus (Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide) supplied by GNH India

Olmedipin Plus

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

Olmedipin Plus (Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide)

Olmesartan medoxomil, the active ingredient in Olmedipin Plus, is a combination antihypertensive presented as a tablet for oral use. It treats hypertension in adults, often when single‑agent therapy is insufficient. GNH India supplies Olmedipin Plus as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

GNH India supplies Olmedipin Plus as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Viatris Limited

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Indications & Clinical Uses

Olmedipin Plus is a combination antihypertensive that addresses elevated blood pressure through multiple pathways.

  • Hypertension: helps achieve target blood pressure when monotherapy does not provide adequate control.
  • Hypertensive urgency: may be used as part of a regimen to lower blood pressure safely under medical supervision.
  • Cardiovascular risk reduction: contributes to lowering the risk of stroke and myocardial infarction in patients with high blood pressure.

How It Works

  • Olmedipin Plus combines three agents that act at different points in blood‑pressure regulation. Olmesartan medoxomil blocks the angiotensin II type‑1 receptor, preventing vasoconstriction. Amlodipine inhibits calcium influx into vascular smooth‑muscle cells, producing arterial dilation. Hydrochlorothiazide increases renal sodium and water excretion, reducing plasma volume. The combined actions produce additive reductions in systemic vascular resistance and circulating volume, lowering blood pressure.

Side Effects

Olmedipin Plus may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Dizziness or light‑headedness
  • Peripheral edema, especially of the lower legs
  • Headache
  • Fatigue
  • Increased urination
  • Mild electrolyte disturbances (e.g., low potassium)

Serious or Rare Side Effects

  • Severe hypotension
  • Acute kidney injury
  • Hyperkalemia or severe electrolyte imbalance
  • Angio‑edema, particularly facial or airway swelling
  • Liver function abnormalities
  • Blood dyscrasias such as neutropenia

Precautions & Warnings

When prescribing Olmedipin Plus, clinicians should consider several safety aspects.

  • Renal function: assess baseline kidney function and monitor periodically.
  • Electrolytes: check serum potassium and sodium levels, especially with diuretic component.
  • Cardiovascular status: avoid rapid blood‑pressure drops in patients with recent myocardial infarction.
  • Pregnancy: contraindicated in the second and third trimesters; use only if benefits outweigh risks.
  • Drug interactions: review concomitant medications for additive hypotensive effects.
  • Store at below 25°C: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Olmedipin Plus can interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Dual renin‑angiotensin system blockade (e.g., ACE inhibitors, other ARBs): risk of severe hypotension and renal impairment.
  • Potassium‑sparing diuretics or supplements: may cause dangerous hyper‑kalemia.
  • Lithium: increased lithium levels and potential toxicity.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may reduce antihypertensive efficacy and affect renal function.
  • CYP3A4 inhibitors (e.g., clarithromycin, itraconazole): can raise amlodipine concentrations.
  • Antidiabetic agents: may enhance glucose‑lowering effect, requiring dose adjustment.

Frequently Asked Questions

Olmedipin Plus is a fixed‑dose combination of olmesartan medoxomil, amlodipine and hydrochlorothiazide that is prescribed to lower high blood pressure in adults, especially when single‑agent therapy does not achieve target levels. It is part of standard antihypertensive regimens aimed at reducing the risk of stroke, heart attack and other cardiovascular complications.

Olmesartan medoxomil is an angiotensin II type‑1 (AT‑1) receptor blocker. By preventing angiotensin II from binding to its receptor, it inhibits vasoconstriction and aldosterone release, leading to relaxed blood vessels and reduced fluid retention, which together lower systemic blood pressure.

The dose of Olmedipin Plus is individualized by the prescribing clinician based on the patient’s blood‑pressure readings, renal function, and overall cardiovascular risk. The prescriber determines the appropriate strength and dosing schedule, which is then reflected on the product label.

Olmesartan medoxomil is contraindicated in the second and third trimesters of pregnancy because of potential fetal toxicity. Amlodipine and hydrochlorothiazide are also not recommended unless the benefits outweigh the risks. Breastfeeding mothers should consult their healthcare provider, as the drugs may pass into breast milk.

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 (including any cold‑chain requirements) and necessary import documentation.

Olmedipin Plus combines an ARB, a calcium‑channel blocker and a thiazide diuretic, offering a broader blood‑pressure‑lowering effect than single‑agent therapies. Compared with other combination products, it provides three complementary mechanisms, which can improve control in patients who need multiple pathways targeted, while potentially reducing pill burden.

Olmedipin Plus tablets should be stored at temperatures below 25 °C, in the original packaging to protect from moisture and direct sunlight. Keep the container tightly closed and out of reach of children.

Olmedipin Plus 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 adverse events can include severe hypotension, acute kidney injury, hyper‑kalemia, angio‑edema and significant electrolyte disturbances. Patients should be monitored for signs such as dizziness, swelling of the face or throat, sudden loss of kidney function, or abnormal blood‑test results.

Olmedipin Plus is contraindicated in patients with known hypersensitivity to any component, those with severe renal impairment, hyper‑kalemia, or in the second and third trimesters of pregnancy. It should also be avoided in individuals taking other ARBs, ACE inhibitors, or potassium‑sparing diuretics without careful medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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