Product image of Nebivolol Teva Uk (Nebivolol) supplied by GNH India

Nebivolol Teva Uk

Active Ingredient:
Nebivolol
Origin:
EU

Nebivolol Teva Uk (Nebivolol)

Nebivolol, the active ingredient in Nebivolol Teva Uk, is a beta‑blocker presented as a tablet for oral use. It is prescribed to lower high blood pressure in adult patients.
GNH India supplies Nebivolol Teva Uk as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva Uk Limited

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Indications & Clinical Uses

Nebivolol is a selective β1‑adrenergic antagonist used primarily in the management of hypertension.

  • Hypertension: reduces systolic and diastolic blood pressure, helping to prevent cardiovascular complications.
  • Chronic heart failure (off‑label in some regions): may improve ventricular function and symptoms when used under specialist supervision.
  • Elderly patients with isolated systolic hypertension: provides blood‑pressure control with a favorable heart‑rate profile.

How It Works

  • Nebivolol selectively blocks β1‑adrenergic receptors in cardiac tissue, decreasing heart rate and contractility, which lowers cardiac output. Concurrently, it stimulates endothelial nitric‑oxide synthase, leading to nitric‑oxide‑mediated vasodilation and reduced peripheral vascular resistance, together producing an antihypertensive effect.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate intensity.
  • Dizziness or light‑headedness: especially after the first dose.
  • Fatigue: a feeling of reduced energy.
  • Nasal congestion: occasional blockage of nasal passages.
  • Bradycardia: slower than normal heart rate.
  • Gastrointestinal discomfort: nausea or abdominal pain.

Serious or Rare Side Effects

  • Severe bradycardia: heart rate markedly below normal.
  • Acute heart failure decompensation.
  • Bronchospasm: especially in patients with reactive airway disease.
  • Hypotension: dangerously low blood pressure.
  • Allergic reactions: rash, itching, or swelling.
  • Liver enzyme elevations: abnormal liver function tests.

Precautions & Warnings

Nebivolol requires careful assessment before initiation and during therapy.

  • Cardiovascular assessment: evaluate heart rate, rhythm, and blood pressure before starting.
  • Concomitant β‑blockers: avoid combining with other β‑blockers to prevent excessive bradycardia.
  • Asthma or COPD: use with caution due to potential bronchospasm.
  • Diabetes mellitus: monitor blood glucose as β‑blockade may mask hypoglycaemia symptoms.
  • Pregnancy and lactation: safety not established; prescribe only if benefits outweigh risks.
  • Store at ambient temperature: keep below 25 °C, in the original container, protected from moisture and light.

Avoid Interactions

Nebivolol can interact with several drug classes, influencing its efficacy and safety.

Major Interactions (Avoid)

  • Strong CYP2D6 inhibitors (e.g., paroxetine, quinidine): may increase nebivolol plasma levels.
  • Non‑dihydropyridine calcium channel blockers (e.g., verapamil, diltiazem): can cause additive bradycardia.
  • Other antihypertensives (e.g., ACE inhibitors, diuretics): may lead to excessive hypotension.

Moderate Interactions (Monitor Closely)

  • Antidiabetic agents: β‑blockade may mask hypoglycaemia signs.
  • NSAIDs: may reduce antihypertensive effect.
  • Antidepressants (e.g., SSRIs): monitor for additive heart‑rate effects.
  • Digoxin: increased risk of bradyarrhythmias.
  • Alcohol: may enhance central nervous system depression and dizziness.

Frequently Asked Questions

Nebivolol Teva Uk is a prescription‑only oral tablet that belongs to the beta‑blocker class. It is primarily used to treat hypertension by lowering elevated blood pressure and reducing the risk of cardiovascular events in adult patients.

Nebivolol selectively blocks β1‑adrenergic receptors in the heart, decreasing heart rate and contractility. At the same time, it enhances nitric‑oxide release from the endothelium, causing vasodilation and lowering peripheral vascular resistance, which together result in reduced blood pressure.

The appropriate dose of nebivolol is determined by a qualified prescriber based on the individual’s clinical condition, age, renal function, and response to therapy. Patients should follow the dosing instructions provided by their healthcare professional.

Safety data for nebivolol in pregnancy and lactation are limited. It should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and this decision must be made by the prescribing clinician.

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.

Nebivolol offers a unique combination of β1‑selectivity and nitric‑oxide‑mediated vasodilation, which can provide effective blood‑pressure control with a lower incidence of metabolic side effects compared with non‑selective beta‑blockers. Its profile differs from ACE inhibitors, calcium‑channel blockers, and diuretics, each of which works via distinct mechanisms.

Nebivolol tablets should be stored at ambient temperature, preferably below 25 °C. Keep them in the original packaging, protect from moisture and direct sunlight, and ensure the container is tightly closed to maintain product stability.

Nebivolol is taken orally, usually once daily, with or without food as directed by the prescriber. The tablet should be swallowed whole with a glass of water and not chewed or crushed unless specifically instructed.

Serious risks include severe bradycardia, hypotension, acute heart‑failure decompensation, bronchospasm in patients with reactive airway disease, and rare allergic reactions. Patients should seek immediate medical attention if they experience fainting, rapid weight gain, swelling, or difficulty breathing.

Nebivolol is contraindicated in patients with known hypersensitivity to the drug, those with severe bradycardia, second‑ or third‑degree atrioventricular block without a pacemaker, and individuals with uncompensated heart failure. Caution is also advised for patients with asthma, COPD, or significant liver impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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