Product image of Nebivolol Accord (Nebivolol Hydrochloride) supplied by GNH India

Nebivolol Accord

Active Ingredient:
Nebivolol Hydrochloride
Origin:
EU

Nebivolol Accord (Nebivolol Hydrochloride)

Nebivolol Hydrochloride, the active ingredient in Nebivolol Accord, is a beta‑blocker presented as an oral tablet for oral use. It is used to treat hypertension and, where approved, heart failure in adult patients.
GNH India supplies Nebivolol Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Accord Healthcare Ireland Limited

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Indications & Clinical Uses

  • Nebivolol Accord is a selective β1‑adrenergic antagonist indicated for cardiovascular conditions that require blood‑pressure control and cardiac workload reduction.
  • Hypertension: lowers systolic and diastolic blood pressure by reducing heart rate and peripheral vascular resistance.
  • Heart failure: improves cardiac output and reduces symptoms by decreasing myocardial oxygen demand and after‑load.

How It Works

  • Nebivolol Hydrochloride selectively blocks β1‑adrenergic receptors in cardiac tissue, decreasing heart rate and contractility. Concurrently, it stimulates endothelial nitric‑oxide release, causing vasodilation and lowering peripheral vascular resistance. The combined effect reduces cardiac workload and systemic blood pressure without significant β2‑receptor antagonism.

Side Effects

Nebivolol Accord may cause a range of adverse reactions.

Common Side Effects

  • Headache: mild to moderate pain often occurring early in therapy.
  • Dizziness: sensation of light‑headedness, especially upon standing.
  • Fatigue: generalized tiredness or reduced energy.
  • Bradycardia: slower than normal heart rate.
  • Nasal congestion: blocked or runny nose.
  • Diarrhea: loose stools occurring intermittently.

Serious or Rare Side Effects

  • Severe bradycardia: markedly low heart rate requiring medical attention.
  • Symptomatic hypotension: significant drop in blood pressure causing faintness.
  • Heart block: impairment of electrical conduction in the heart.
  • Bronchospasm: narrowing of airways, particularly in patients with asthma.
  • Allergic reactions: rash, itching, swelling, or anaphylaxis.
  • Hepatic dysfunction: abnormal liver enzyme elevations.

Precautions & Warnings

  • Before initiating therapy, consider the following safety measures.
  • Dose adjustment in renal impairment: reduce dose in patients with reduced kidney function.
  • Caution in asthma or COPD: monitor for bronchospasm due to β‑blockade.
  • Monitor heart rate and blood pressure: ensure values remain within therapeutic range.
  • Avoid abrupt discontinuation: taper gradually to prevent rebound hypertension.
  • Use with caution in diabetes: may mask hypoglycaemic symptoms.
  • Store at room temperature: keep in the original pack, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Concomitant use with other beta‑blockers: additive cardiac depression.
  • Calcium channel blockers that affect AV node (e.g., verapamil, diltiazem): risk of severe bradycardia.
  • Strong CYP2D6 inhibitors (e.g., paroxetine, fluoxetine): increased nebivolol plasma levels.

Moderate Interactions (Monitor Closely)

  • Diuretics: may enhance hypotensive effect.
  • ACE inhibitors or ARBs: additive blood‑pressure lowering.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may reduce antihypertensive efficacy.

Frequently Asked Questions

Nebivolol Accord is prescribed for managing high blood pressure (hypertension) and, where approved, for treating heart failure. It works by lowering heart rate and relaxing blood vessels, which helps reduce the workload on the heart and improves circulation.

Nebivolol hydrochloride selectively blocks β1‑adrenergic receptors in the heart, decreasing heart rate and contractility. At the same time, it stimulates endothelial nitric‑oxide release, causing vasodilation and lowering peripheral vascular resistance, which together lower blood pressure.

The appropriate dose of Nebivolol Accord is determined by a qualified prescriber based on the individual’s medical condition, response to therapy, and any concomitant medications. Patients should follow the dosing instructions provided by their healthcare professional.

Safety data for nebivolol during pregnancy and lactation are limited, and the product’s pregnancy category is listed as unknown. 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 healthcare provider.

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 selective β1‑blocker with additional nitric‑oxide‑mediated vasodilation, which may result in fewer metabolic side effects compared with non‑selective beta‑blockers. Its unique profile can offer better tolerability in some patients, but the choice of therapy should be individualized by the prescriber.

Nebivolol Accord should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, heat, and direct sunlight to maintain its stability and potency throughout its shelf life.

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

Serious risks include severe bradycardia, symptomatic hypotension, heart block, bronchospasm in patients with reactive airway disease, and rare allergic reactions such as anaphylaxis. Patients should seek immediate medical attention if they experience fainting, rapid heartbeat, difficulty breathing, or signs of an allergic response.

Nebivolol Accord is contraindicated in patients with known hypersensitivity to nebivolol or any excipients, those with severe sinus bradycardia, second‑ or third‑degree atrioventricular block without a pacemaker, and individuals with uncompensated heart failure. A prescriber must evaluate each patient’s medical history before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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