Product image of Nebivolol/Hct Eg (Hydrochlorothiazide, Nebivolol) supplied by GNH India

Nebivolol/Hct Eg

Active Ingredient:
Hydrochlorothiazide, Nebivolol
Origin:
EU

Nebivolol/Hct Eg (Hydrochlorothiazide, Nebivolol)

Nebivolol, the active ingredient in Nebivolol/Hct Eg, is a beta‑blocker presented as an oral tablet for oral use. It is combined with hydrochlorothiazide to treat essential hypertension in adult patients, helping to lower elevated blood pressure and reduce cardiovascular risk.
GNH India supplies Nebivolol/Hct Eg as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Eurogenerics N.V./S.A.

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Indications & Clinical Uses

Nebivolol/Hydrochlorothiazide is indicated for the management of hypertension, acting on the cardiovascular system to control elevated blood pressure.

  • Essential hypertension: lowers systolic and diastolic pressure in patients with primary high blood pressure.
  • Hypertension requiring diuretic therapy: provides additive blood‑pressure reduction through combined beta‑blockade and diuresis.
  • Stage 1 hypertension: assists in achieving target blood‑pressure goals when lifestyle measures are insufficient.

How It Works

  • Nebivolol selectively blocks β1‑adrenergic receptors, reducing heart rate and myocardial contractility while also stimulating endothelial nitric‑oxide release, causing vasodilation. Hydrochlorothiazide inhibits sodium‑chloride reabsorption in the distal convoluted tubule, increasing urinary sodium and water excretion, which decreases plasma volume and peripheral resistance. Together, these actions synergistically lower systemic blood pressure.

Side Effects

Common Side Effects

  • Dizziness: sensation of light‑headedness, especially after standing.
  • Headache: mild to moderate pain often related to blood‑pressure changes.
  • Fatigue: reduced energy or feeling unusually tired.
  • Increased urination: due to the diuretic component.
  • Electrolyte imbalance: mild changes in potassium or sodium levels.

Serious or Rare Side Effects

  • Severe hypotension: markedly low blood pressure requiring medical attention.
  • Acute kidney injury: sudden decline in renal function.
  • Hyperuricemia or gout flare: elevated uric acid levels.
  • Anaphylactic reaction: rare severe allergic response.

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.
  • Diabetes management: monitor blood‑glucose as beta‑blockers may mask hypoglycaemia symptoms.
  • Hepatic impairment: use with caution in severe liver disease.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nebivolol/Hydrochlorothiazide may interact with several medicines.

Major Interactions (Avoid)

  • Other antihypertensives (e.g., ACE inhibitors, ARBs): additive blood‑pressure lowering effect may cause hypotension.
  • Potassium‑sparing diuretics or supplements: risk of hyperkalaemia.
  • NSAIDs (e.g., ibuprofen): may reduce diuretic efficacy and impair renal function.

Moderate Interactions (Monitor Closely)

  • CYP2D6 inhibitors (e.g., fluoxetine, paroxetine): may increase nebivolol plasma levels.
  • Lithium: concurrent use can raise lithium concentrations, risking toxicity.
  • Antidiabetic agents: beta‑blockade may mask hypoglycaemia signs, requiring dose adjustments.

Frequently Asked Questions

Nebivolol/Hct Eg is a prescription combination of nebivolol and hydrochlorothiazide indicated for the treatment of essential hypertension. It helps lower high blood pressure by combining a beta‑blocker with a thiazide diuretic, providing a dual mechanism to achieve better blood‑pressure control in adult patients.

Nebivolol selectively blocks β1‑adrenergic receptors, reducing heart rate and contractility, while also enhancing nitric‑oxide release from the endothelium, which promotes vasodilation. This action lowers cardiac output and peripheral resistance, contributing to overall blood‑pressure reduction.

The specific dose and dosing schedule of Nebivolol/Hct Eg are determined by the prescribing clinician based on the patient’s medical condition, response to therapy, and other individual factors. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

The safety of Nebivolol/Hct Eg in pregnancy and lactation has not been established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and this decision must be made by a qualified healthcare professional.

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.

Compared with single‑agent therapies, the nebivolol/hydrochlorothiazide combination offers both beta‑blockade and diuretic effects in one tablet, which can improve adherence and provide greater blood‑pressure reduction than either component alone. It is an alternative to other fixed‑dose combos such as atenolol/diuretic or ACE‑inhibitor/diuretic regimens.

Nebivolol/Hct Eg should be stored at room temperature, below 25 °C, in the original packaging to protect it from moisture and light. Keep the product out of reach of children and do not use it after the expiry date printed on the label.

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

Serious risks include severe hypotension, acute kidney injury, electrolyte disturbances such as hyperkalaemia or hyponatraemia, and rare allergic reactions like anaphylaxis. Patients should seek immediate medical attention if they experience fainting, rapid weight gain, swelling, or signs of an allergic reaction.

Nebivolol/Hct Eg is contraindicated in patients with known hypersensitivity to nebivolol, hydrochlorothiazide, or any excipients, as well as those with severe bradycardia, second‑ or third‑degree heart block, or uncontrolled heart failure. Caution is also advised for individuals with severe renal or hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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