Product image of Nebivololo E Idroclorotiazide Eg (Hydrochlorothiazide, Nebivolol) supplied by GNH India

Nebivololo E Idroclorotiazide Eg

Active Ingredient:
Hydrochlorothiazide, Nebivolol
Origin:
EU

Nebivololo E Idroclorotiazide Eg (Hydrochlorothiazide, Nebivolol)

Nebivolol, the active ingredient in Nebivolol/Hydrochlorothiazide, is a beta‑blocker presented as a tablet for oral use. It works together with hydrochlorothiazide to lower blood pressure in adult patients diagnosed with hypertension and is commonly prescribed.

GNH India supplies Nebivolol/Hydrochlorothiazide as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable access to quality‑assured antihypertensive medicines. The product complies with EU regulatory standards and is manufactured under GMP conditions, ensuring consistent potency and safety for patients across diverse markets.

Manufacturer / TM Owner

Eg S.P.A.

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Indications & Clinical Uses

Nebivolol/Hydrochlorothiazide is an antihypertensive combination that targets blood pressure regulation.

  • Hypertension: lowers systolic and diastolic blood pressure in adult patients.
  • Essential hypertension: improves overall blood pressure control when monotherapy is insufficient.
  • High blood pressure: assists in achieving target blood pressure levels as part of a therapeutic regimen.

How It Works

  • Nebivolol selectively blocks β1‑adrenergic receptors, reducing heart rate and contractility while also enhancing nitric‑oxide mediated vasodilation. Hydrochlorothiazide inhibits Na⁺/Cl⁻ reabsorption in the distal convoluted tubule, increasing urinary sodium and water excretion, which decreases plasma volume and peripheral resistance, together producing an additive antihypertensive effect.

Side Effects

Adverse reactions may occur with nebivolol/hydrochlorothiazide therapy.

Common Side Effects

  • Dizziness: transient light‑headedness, especially after standing.
  • Headache: mild to moderate intensity.
  • Fatigue: feeling of tiredness or reduced energy.
  • Increased urination: due to diuretic action.
  • Electrolyte imbalance: mild changes in potassium or sodium levels.
  • Nausea: occasional stomach upset.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure causing fainting.
  • Electrolyte disturbances: significant hyponatremia or hypokalemia.
  • Acute kidney injury: sudden reduction in renal function.
  • Pancreatitis: inflammation of the pancreas.
  • Anaphylaxis: rare severe allergic reaction.

Precautions & Warnings

Before initiating therapy, consider the following precautions.

  • Blood pressure monitoring: ensure adequate control and avoid excessive drops.
  • Renal function assessment: evaluate kidney function, especially in patients with pre‑existing impairment.
  • Electrolyte surveillance: check serum potassium and sodium periodically.
  • Caution in asthma/COPD: beta‑blockade may exacerbate bronchospasm.
  • Avoid abrupt discontinuation: taper gradually to prevent rebound hypertension.
  • Store at below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Nebivolol/hydrochlorothiazide may interact with other medicines.

Major Interactions (Avoid)

  • Other antihypertensives: additive blood‑pressure lowering effect may cause hypotension.
  • Potassium‑sparing diuretics: risk of hyperkalemia.
  • Lithium: increased lithium levels leading to toxicity.
  • NSAIDs: may reduce diuretic efficacy and impair renal function.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: monitor renal function and potassium.
  • Digoxin: increased risk of digoxin toxicity.
  • Antidiabetic agents: may enhance hypoglycaemic effect, requiring dose adjustment.

Frequently Asked Questions

Nebivolol/Hydrochlorothiazide is prescribed to treat hypertension. The combination lowers blood pressure by reducing heart rate and cardiac output through nebivolol, while hydrochlorothiazide promotes fluid loss and decreases plasma volume, together helping patients achieve target blood‑pressure goals.

Nebivolol selectively blocks β1‑adrenergic receptors, which slows heart rate and reduces contractility. It also stimulates nitric‑oxide release, causing vasodilation. This dual action lowers cardiac output and peripheral resistance, contributing to overall blood‑pressure reduction.

The specific dose is determined by the prescribing clinician based on the individual’s medical condition, response to therapy, and other medications. Dosage adjustments are made to achieve optimal blood‑pressure control while minimizing adverse effects.

Safety in pregnancy and lactation has not been fully established. Healthcare providers should weigh potential benefits against possible risks and consider alternative treatments if safer options are available for pregnant or nursing individuals.

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‑component agents, this combination offers complementary mechanisms—beta‑blockade and diuresis—allowing better blood‑pressure control in patients who need more than one pathway. It may reduce the number of pills required versus separate prescriptions, but individual response and tolerance vary.

Store the tablets at temperatures below 25 °C in their original container, protecting them from moisture and direct sunlight. Do not expose the product to excessive heat or humidity, and keep it out of reach of children.

The medication is taken orally, usually once daily, with or without food, as directed by a healthcare professional. Swallow the tablet whole with a full glass of water; do not crush or chew unless specifically instructed.

Serious risks include severe hypotension, significant electrolyte disturbances (such as hyponatremia or hypokalemia), acute kidney injury, and rare allergic reactions like anaphylaxis. Patients should seek immediate medical attention if they experience fainting, rapid weight loss, muscle cramps, or signs of an allergic response.

Individuals with known hypersensitivity to nebivolol, hydrochlorothiazide, or any component of the formulation should avoid this product. It is also contraindicated in patients with severe bradycardia, advanced heart block without a pacemaker, or those with uncontrolled electrolyte imbalances.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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