Product image of Nebivololo Pensa (Nebivolol Hydrochloride) supplied by GNH India

Nebivololo Pensa

Active Ingredient:
Nebivolol Hydrochloride
Origin:
EU

Nebivololo Pensa (Nebivolol Hydrochloride)

Nebivolol, the active ingredient in Nebivololo Pensa, is a beta‑blocker presented as an oral tablet for oral use. It treats hypertension and may be used in certain cases of heart failure in adult patients.
GNH India supplies Nebivololo Pensa as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Towa Pharmaceutical S.P.A.

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Indications & Clinical Uses

Nebivolol is a selective β1‑adrenergic antagonist used primarily in cardiovascular therapy.

  • Hypertension: lowers systolic and diastolic blood pressure, reducing risk of stroke and myocardial infarction.
  • Chronic heart failure: improves left‑ventricular ejection fraction and decreases hospitalization rates.
  • Chronic stable angina: reduces frequency of chest pain episodes by decreasing myocardial oxygen demand.

How It Works

  • Nebivolol selectively blocks β1‑adrenergic receptors in cardiac tissue, diminishing heart rate and contractility. Concurrently, it stimulates endothelial nitric‑oxide synthase, leading to nitric‑oxide‑mediated vasodilation, which lowers peripheral vascular resistance and contributes to overall blood pressure reduction.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate intensity.
  • Dizziness: especially on standing (orthostatic).
  • Fatigue: feeling of tiredness or lack of energy.
  • Nasal congestion: mild blockage of nasal passages.
  • Diarrhea: loose stools, usually transient.
  • Bradycardia: heart rate below normal range.

Serious or Rare Side Effects

  • Severe bradycardia: may require medical attention.
  • Heart block: atrioventricular conduction disturbances.
  • Acute heart failure decompensation.
  • Bronchospasm: especially in patients with reactive airway disease.
  • Hypotension: marked drop in blood pressure causing syncope.
  • Liver enzyme elevation: abnormal hepatic function tests.

Precautions & Warnings

Before initiating therapy, consider the following safety measures.

  • Cardiovascular assessment: evaluate heart rate, blood pressure, and cardiac function.
  • Respiratory disease: avoid in uncontrolled asthma or severe COPD.
  • Diabetes monitoring: may mask hypoglycaemia symptoms.
  • Renal impairment: adjust dose in severe renal dysfunction.
  • Drug interactions: review concomitant medications for potential additive effects.
  • Store at ambient temperature: keep below 25°C, retain in original container, protect from moisture and light.

Avoid Interactions

Nebivolol may interact with several drug classes; awareness helps prevent adverse outcomes.

Major Interactions (Avoid)

  • Combined β‑blockers: additive bradycardia and hypotension.
  • Strong CYP2D6 inhibitors (e.g., paroxetine, quinidine): markedly increase nebivolol plasma levels.
  • Calcium channel blockers (verapamil, diltiazem): risk of severe bradycardia.

Moderate Interactions (Monitor Closely)

  • Diuretics: may potentiate hypotensive effect.
  • Antidiabetic agents: monitor blood glucose as symptoms of hypoglycaemia may be blunted.
  • NSAIDs: can reduce antihypertensive efficacy.
  • Antidepressants (tricyclics): may increase risk of cardiac conduction abnormalities.

Frequently Asked Questions

Nebivololo Pensa contains nebivolol, a selective β1‑adrenergic blocker indicated for the treatment of hypertension and, in some regions, chronic heart failure. It helps lower blood pressure and improve cardiac function.

Nebivolol blocks β1‑adrenergic receptors in the heart, reducing heart rate and contractility. It also stimulates nitric‑oxide release from the endothelium, causing vasodilation and further lowering peripheral resistance.

The dose of nebivolol is individualized by the prescribing clinician based on the patient’s condition, age, renal function, and response to therapy. Dosage adjustments are made according to clinical guidelines.

Safety data for nebivolol in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the 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 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 distinguished by its additional nitric‑oxide‑mediated vasodilatory effect, which can result in fewer metabolic side effects compared with non‑vasodilating beta‑blockers. It offers comparable blood‑pressure control while potentially improving endothelial function.

Store Nebivololo Pensa tablets at ambient temperature, below 25 °C. Keep the product in its original packaging, protect it from moisture and direct sunlight, and ensure the container is tightly closed.

Nebivololo Pensa is taken orally, usually once daily with or without food, as directed by the prescribing physician. Swallow the tablet whole; do not crush or chew unless instructed otherwise.

Serious risks include severe bradycardia, heart block, marked hypotension, and worsening heart failure. Patients should be monitored for signs of these conditions, especially during dose initiation or adjustment.

Nebivolol is contraindicated in patients with known hypersensitivity to the drug, severe bradycardia, second‑ or third‑degree atrioventricular block, cardiogenic shock, and uncontrolled asthma or severe chronic obstructive pulmonary disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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