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

Nebivolol Teva

Active Ingredient:
Nebivolol Hydrochloride
Origin:
EU

Nebivolol Teva (Nebivolol Hydrochloride)

Nebivolol, the active ingredient in Nebivolol Teva, is a beta blocker presented as an oral tablet for oral use. It is used to lower elevated blood pressure in adult patients and helps reduce cardiovascular risk associated with hypertension.

GNH India supplies Nebivolol Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory‑approved batches to meet global demand. Our distribution network ensures timely delivery and reliable product integrity across diverse markets.

Manufacturer / TM Owner

Teva Pharma – Produtos Farmacêuticos Lda

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Indications & Clinical Uses

  • Nebivolol is a selective β1‑adrenergic blocker indicated for the management of hypertension.
  • Hypertension: reduces systolic and diastolic blood pressure, improving cardiovascular outcomes.
  • Chronic heart failure: lowers mortality and hospitalization rates by improving cardiac function.

How It Works

  • Nebivolol selectively antagonizes β1‑adrenergic receptors in cardiac tissue, decreasing heart rate and contractility, which reduces cardiac output. Concurrently, it stimulates endothelial nitric oxide synthase, leading to nitric oxide‑mediated vasodilation and further lowering of peripheral vascular resistance, thereby contributing to blood pressure reduction.

Side Effects

Nebivolol may cause a range of adverse reactions, which are categorized by frequency.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Dizziness or light‑headedness, especially on standing.
  • Fatigue or general tiredness.
  • Nasal congestion or rhinorrhea.
  • Gastrointestinal discomfort, such as nausea.
  • Insomnia or sleep disturbances.

Serious or Rare Side Effects

  • Bradycardia: markedly reduced heart rate requiring medical attention.
  • Severe hypotension: sudden drop in blood pressure leading to fainting.
  • Cardiac conduction abnormalities, including heart block.
  • Acute bronchospasm in susceptible individuals.
  • Anaphylactic or severe allergic reactions.

Precautions & Warnings

  • Nebivolol should be used with caution in specific clinical situations.
  • Monitor blood pressure: ensure adequate control without excessive lowering.
  • Assess cardiac function: evaluate heart rate and rhythm regularly.
  • Use cautiously in asthma or COPD: beta‑blockade may exacerbate bronchospasm.
  • Avoid abrupt discontinuation: taper dose to prevent rebound hypertension.
  • Adjust in hepatic impairment: consider dose reduction if liver function is compromised.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nebivolol can interact with several medication classes; awareness of major and moderate interactions helps optimize therapy.

Major Interactions (Avoid)

  • Combined use with other beta‑blockers: may cause excessive bradycardia.
  • Non‑selective beta‑blockers (e.g., propranolol): increased risk of cardiac depression.
  • Calcium channel blockers verapamil or diltiazem: can potentiate negative inotropic effects.
  • Strong CYP2D6 inhibitors (e.g., quinidine, paroxetine): raise nebivolol plasma levels.
  • Antihypertensive agents causing profound hypotension.

Moderate Interactions (Monitor Closely)

  • Diuretics: may enhance hypotensive effect.
  • ACE inhibitors or ARBs: monitor for additive blood pressure reduction.
  • NSAIDs: may attenuate antihypertensive response.
  • Antidiabetic drugs: monitor blood glucose as beta‑blockade can mask hypoglycemia.
  • Other vasodilators: watch for excessive vasodilation.

Frequently Asked Questions

Nebivolol Teva contains the beta‑blocker nebivolol, which is prescribed to lower high blood pressure in adult patients. By reducing systolic and diastolic pressures, it helps lower the risk of cardiovascular events associated with hypertension.

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 reducing peripheral vascular resistance, which together lower arterial pressure.

The appropriate dose of Nebivolol Teva is determined by the prescribing healthcare professional based on the patient’s condition, response, and any comorbidities. Dosage adjustments may be needed for special populations, and patients should follow the prescriber’s instructions.

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 provider.

To request Nebivolol Teva, 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 β1‑selective blocker with added nitric‑oxide‑mediated vasodilation, offering a dual mechanism that can improve tolerability compared with non‑selective beta‑blockers. It may be preferred in patients who need heart‑rate control and benefit from vasodilatory effects, while other classes such as ACE inhibitors or calcium‑channel blockers work via different pathways.

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

Serious risks include marked bradycardia, severe hypotension, heart block, and rare allergic reactions such as anaphylaxis. Patients should seek immediate medical attention if they experience fainting, unusually slow heart rate, chest pain, or signs of a severe allergic response.

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

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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