Product image of Nebivolol Biogaran (Nebivolol) supplied by GNH India

Nebivolol Biogaran

Active Ingredient:
Nebivolol
Origin:
EU

Nebivolol Biogaran (Nebivolol)

Nebivolol, the active ingredient in Nebivolol Biogaran, is a beta blocker presented as an oral tablet for oral use. It is used to lower high blood pressure and to improve outcomes in patients with heart failure.
GNH India supplies Nebivolol Biogaran as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Biogaran

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Indications & Clinical Uses

Nebivolol belongs to the beta‑blocker class and is indicated for cardiovascular conditions where reduction of sympathetic activity is required.

  • Hypertension: lowers systolic and diastolic blood pressure to reduce cardiovascular risk.
  • Heart failure: improves left‑ventricular ejection fraction and decreases hospitalization rates.
  • Elevated blood pressure in patients with diabetes: helps achieve target blood pressure while offering metabolic neutrality.

How It Works

  • Nebivolol selectively blocks β1‑adrenergic receptors in cardiac tissue, reducing heart rate and contractility. In addition, it stimulates endothelial nitric oxide synthase, causing nitric‑oxide‑mediated vasodilation, which further contributes to blood‑pressure reduction without significant β2 blockade.

Side Effects

Nebivolol is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Dizziness or light‑headedness, especially on standing.
  • Fatigue or tiredness during initial therapy.
  • Nausea or mild gastrointestinal upset.
  • Bradycardia: heart rate slower than normal.
  • Nasal congestion or sinusitis.

Serious or Rare Side Effects

  • Severe bradycardia or heart block requiring medical attention.
  • Acute bronchospasm in patients with asthma or COPD.
  • Allergic reactions such as rash, itching, or angioedema.
  • Hepatic dysfunction manifested by elevated liver enzymes.
  • Cardiogenic shock in patients with decompensated heart failure.

Precautions & Warnings

Nebivolol requires careful assessment before and during therapy.

  • Blood pressure monitoring: ensure target levels are reached without excessive drop.
  • Cardiac function evaluation: baseline ECG and periodic checks for bradycardia.
  • Respiratory caution: avoid in uncontrolled asthma or severe COPD.
  • Renal impairment: dose adjustment may be needed in moderate to severe dysfunction.
  • Discontinuation: taper gradually to prevent rebound hypertension.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nebivolol can interact with several drug classes, requiring clinical vigilance.

Major Interactions (Avoid)

  • Other beta‑blockers: additive negative chronotropic effects.
  • Calcium‑channel blockers verapamil or diltiazem: may cause profound bradycardia or AV block.
  • Strong CYP2D6 inhibitors (e.g., paroxetine, fluoxetine): increase nebivolol plasma concentrations.

Moderate Interactions (Monitor Closely)

  • Diuretics: may enhance antihypertensive effect, risking hypotension.
  • ACE inhibitors or ARBs: combined use can improve blood‑pressure control but requires monitoring of renal function.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may blunt antihypertensive response.
  • Antidiabetic agents: monitor blood glucose as beta‑blockade can mask hypoglycemia symptoms.
  • Antidepressants (other than CYP2D6 inhibitors): watch for additive central nervous system effects.

Frequently Asked Questions

Nebivolol Biogaran is prescribed to lower high blood pressure (hypertension) and to improve heart function in patients with chronic heart failure. It may also be considered for patients with diabetes who need tighter blood‑pressure control, as it does not adversely affect glucose metabolism.

Nebivolol blocks β1‑adrenergic receptors in the heart, reducing heart rate and contractile force. Simultaneously, it enhances nitric‑oxide release from the endothelium, causing vasodilation of peripheral vessels. This dual action lowers systemic vascular resistance and blood pressure without significant β2‑related bronchoconstriction.

The exact dose of nebivolol is determined by the prescribing clinician based on the patient’s medical history, blood‑pressure readings, and response to therapy. Dosage may be started low and titrated upward, but the specific regimen should follow the prescriber’s instructions.

Nebivolol is classified as Pregnancy Category B, indicating that animal studies have not shown risk, but there are no adequate controlled studies in pregnant women. It should be used only if the potential benefit justifies the potential risk. Breastfeeding mothers should consult their physician, as the drug is excreted in 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 and any necessary import documentation.

Nebivolol is a highly selective β1‑blocker with additional nitric‑oxide‑mediated vasodilation, which can result in fewer metabolic side effects and better tolerability compared with non‑selective beta‑blockers. Its unique vasodilatory property may offer an advantage in patients who experience fatigue or cold extremities with traditional agents.

Nebivolol Biogaran tablets should be stored at room temperature, below 25 °C, in the original packaging to protect them from moisture and light. Keep the container tightly closed and out of reach of children.

Nebivolol Biogaran is taken orally, usually once daily with or without food. The tablet should be swallowed whole with a glass of water. Patients should follow the dosing schedule prescribed by their healthcare provider and not skip doses.

Serious risks include severe bradycardia, heart block, and bronchospasm in patients with underlying asthma or COPD. Rarely, allergic reactions such as angioedema or significant liver enzyme elevations may occur. Patients should seek immediate medical attention if they experience fainting, severe shortness of breath, or signs of an allergic reaction.

Nebivolol is contraindicated in patients with severe sinus bradycardia, second‑ or third‑degree atrioventricular block, decompensated heart failure, or uncontrolled asthma/COPD. It should also be avoided in individuals with known hypersensitivity to nebivolol or any of the tablet’s excipients.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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