Product image of Nebivolol/Hydrochlorothiazide Biogaran (Hydrochlorothiazide, Nebivolol) supplied by GNH India

Nebivolol/Hydrochlorothiazide Biogaran

Active Ingredient:
Hydrochlorothiazide, Nebivolol
Origin:
EU

Nebivolol/Hydrochlorothiazide Biogaran (Hydrochlorothiazide, Nebivolol)

Nebivolol, the active ingredient in Nebivolol/Hydrochlorothiazide Biogaran, is a beta‑blocker presented as a combined oral tablet for oral use. In combination with hydrochlorothiazide, a thiazide diuretic, the formulation reduces cardiac output and plasma volume, providing effective blood‑pressure control for adult patients diagnosed with hypertension.

GNH India supplies Nebivolol/Hydrochlorothiazide 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/Hydrochlorothiazide acts on the cardiovascular system to manage elevated blood pressure.

  • Hypertension: lowers systolic and diastolic blood pressure in adults with essential hypertension.
  • Hypertensive chronic kidney disease: assists in controlling blood pressure to slow renal progression.
  • Hypertension with diabetes: provides blood‑pressure reduction without adversely affecting glucose metabolism.

How It Works

  • Nebivolol selectively blocks β1‑adrenergic receptors, decreasing heart rate and myocardial contractility, while also enhancing nitric‑oxide mediated vasodilation. Hydrochlorothiazide inhibits Na⁺/Cl⁻ reabsorption in the distal convoluted tubule, increasing urinary sodium and water excretion, which reduces plasma volume. The combined actions result in a synergistic reduction of arterial pressure.

Side Effects

Common Side Effects

  • Dizziness: light‑headed sensation, especially after standing.
  • Headache: mild to moderate intensity.
  • Fatigue: feeling of tiredness or reduced energy.
  • Increased urination: due to diuretic effect.
  • Electrolyte imbalance: mild changes in potassium or sodium levels.

Serious or Rare Side Effects

  • Severe hypotension: markedly low blood pressure requiring medical attention.
  • Acute renal impairment: sudden decline in kidney function.
  • Hyperuricemia or gout flare: elevated uric acid levels.
  • Allergic reactions: rash, itching, or swelling of face and throat.

Precautions & Warnings

Before initiating therapy, consider the following precautions:

  • Monitor blood pressure: ensure adequate control and avoid excessive drops.
  • Assess renal function: check creatinine and eGFR periodically.
  • Check electrolytes: especially potassium and sodium levels.
  • Avoid abrupt discontinuation: taper to prevent rebound hypertension.
  • Caution in asthma or severe COPD: β1‑selectivity may still affect bronchial tone.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Nebivolol/Hydrochlorothiazide may interact with several drug classes.

Major Interactions (Avoid)

  • Concomitant antihypertensives (e.g., ACE inhibitors, ARBs): risk of additive hypotension.
  • Potassium‑sparing diuretics or supplements: may cause hyperkalemia.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): can diminish diuretic efficacy and affect renal function.

Moderate Interactions (Monitor Closely)

  • β‑agonist bronchodilators: may reduce β‑blocker effectiveness.
  • Lithium: diuretic may increase lithium levels, requiring monitoring.
  • Antidiabetic agents: blood‑glucose may fall, necessitating dose adjustments.

Frequently Asked Questions

Nebivolol/Hydrochlorothiazide Biogaran is an oral combination medication indicated for the treatment of hypertension in adult patients. It lowers elevated blood pressure by reducing heart rate and cardiac output through the beta‑blocker component and by decreasing plasma volume via the thiazide diuretic component.

Nebivolol selectively blocks β1‑adrenergic receptors, which slows the heart rate and reduces myocardial contractility. It also stimulates nitric‑oxide release, leading to vasodilation. Together with hydrochlorothiazide’s diuretic action, this results in a synergistic reduction of arterial pressure.

The appropriate dose is determined by the prescribing healthcare professional based on the individual’s clinical condition, response to therapy, and any concomitant medications. Patients should follow the prescriber’s instructions and not alter the dose without medical advice.

Safety data for use during pregnancy or lactation are limited. The medication should only be used if the potential benefit justifies the potential risk to the fetus or infant. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss alternatives with their healthcare provider.

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. After verification of trade or institutional credentials, the sales team will provide pricing, availability, shipping details and any necessary import documentation.

Nebivolol/Hydrochlorothiazide combines a β1‑selective blocker with a thiazide diuretic, offering both heart‑rate reduction and volume depletion. Compared with monotherapy agents such as ACE inhibitors or calcium‑channel blockers, this combination can achieve blood‑pressure control with a single pill, potentially improving adherence, but individual tolerability and comorbidities guide the choice of therapy.

Store the tablets at temperatures below 25 °C in their original container, protected from moisture and direct sunlight. Keep out of reach of children and do not use after the expiry date printed on the packaging.

The medication is taken orally, usually once daily, with or without food. Tablets should be swallowed whole with a full glass of water and not chewed, crushed, or split unless specifically instructed by a healthcare professional.

Serious adverse events can include severe hypotension, acute renal impairment, marked electrolyte disturbances (especially low potassium), hyperuricemia leading to gout, and rare allergic reactions such as angioedema. Patients should seek immediate medical attention if they experience symptoms like fainting, rapid weight gain, swelling, or difficulty breathing.

The combination is contraindicated in patients with known hypersensitivity to nebivolol, hydrochlorothiazide, or any excipients, as well as those with severe bradycardia, second‑ or third‑degree atrioventricular block, uncompensated heart failure, severe renal impairment, or anuria. Caution is also advised in individuals with asthma, severe hepatic disease, or gout.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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