Product image of Nebivololo E Idroclorotiazide Accord (Hydrochlorothiazide, Nebivolol) supplied by GNH India

Nebivololo E Idroclorotiazide Accord

Active Ingredient:
Hydrochlorothiazide, Nebivolol
Origin:
EU

Nebivololo E Idroclorotiazide Accord (Hydrochlorothiazide, Nebivolol)

Nebivolol, the active ingredient in Nebivololo E Idroclorotiazide Accord, is a beta‑blocker presented as an oral tablet for oral use. It treats hypertension, often in combination with hydrochlorothiazide, and is prescribed for adult patients who need effective blood‑pressure control. Nebivolol works together with the thiazide diuretic to lower vascular resistance and reduce plasma volume.

GNH India supplies Nebivololo E Idroclorotiazide Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Accord Healthcare S.L.U.

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Indications & Clinical Uses

Nebivolol/Hydrochlorothiazide is used to manage high blood pressure and related cardiovascular risk factors.

  • Essential hypertension: lowers systolic and diastolic pressure to reduce cardiovascular events.
  • Secondary hypertension: assists in controlling blood pressure when caused by other medical conditions.
  • Hypertension with fluid retention: combines beta‑blockade and diuresis to manage both pressure and excess fluid.

How It Works

  • Nebivolol selectively blocks β1‑adrenergic receptors, decreasing heart rate and myocardial contractility, while also stimulating endothelial nitric‑oxide release for vasodilation. Hydrochlorothiazide inhibits Na⁺/Cl⁻ reabsorption in the distal convoluted tubule, promoting diuresis, reducing plasma volume, and further decreasing peripheral vascular resistance, together achieving blood‑pressure reduction.

Side Effects

Nebivolol/Hydrochlorothiazide may cause a range of adverse reactions.

Common Side Effects

  • Headache: mild to moderate discomfort.
  • Dizziness or light‑headedness: especially on standing.
  • Fatigue: general tiredness.
  • Increased urination: due to diuretic effect.
  • Electrolyte imbalance: low potassium or sodium.
  • Cough: occasional irritation of the airway.

Serious or Rare Side Effects

  • Severe hypotension: dangerously low blood pressure.
  • Bradycardia: markedly reduced heart rate.
  • Acute kidney injury: sudden decline in renal function.
  • Hyperglycaemia: elevated blood glucose levels.
  • Allergic reactions: rash, swelling, or anaphylaxis.
  • Electrolyte disturbances: severe hyponatraemia or hypokalaemia.

Precautions & Warnings

Before initiating therapy, consider patient‑specific factors and monitor appropriately.

  • Renal impairment: assess kidney function and adjust dosage if needed.
  • Hepatic disease: use with caution in patients with liver dysfunction.
  • Diabetes mellitus: monitor blood glucose as thiazides may raise glucose levels.
  • Electrolyte disorders: check serum potassium and sodium regularly.
  • Concomitant antihypertensives: avoid excessive blood‑pressure lowering.
  • Pregnancy and lactation: safety not established; use only if benefits outweigh risks.
  • Store at ambient temperature: keep below 25°C, retain in original packaging, protect from moisture.

Avoid Interactions

Nebivolol/Hydrochlorothiazide can interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Non‑selective β‑blockers: additive bradycardia and hypotension.
  • Potassium‑sparing diuretics or supplements: risk of hyperkalaemia.
  • Strong CYP2D6 inhibitors (e.g., fluoxetine, paroxetine): increase nebivolol plasma levels.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: may enhance hypotensive effect.
  • NSAIDs: can reduce diuretic efficacy and impair renal function.
  • Lithium: thiazide may increase lithium concentrations.
  • Antidiabetic agents: thiazide may elevate blood glucose, requiring dose adjustment.

Frequently Asked Questions

Nebivololo E Idroclorotiazide Accord is a fixed‑dose combination of nebivolol and hydrochlorothiazide indicated for the treatment of hypertension. It helps lower blood pressure by reducing heart rate, dilating blood vessels, and promoting the excretion of excess fluid.

Nebivolol selectively blocks β1‑adrenergic receptors, decreasing heart rate and contractility, while also enhancing nitric‑oxide release, which relaxes blood vessels. This dual action lowers cardiac output and peripheral resistance, contributing to blood‑pressure reduction.

The specific dose and dosing schedule are determined by the prescribing clinician based on individual patient factors such as blood‑pressure level, renal function, and concomitant medications. Patients should follow the prescriber’s instructions precisely.

Safety in pregnancy and lactation has not been fully established. The product should only be used if the potential benefit justifies the potential risk to the fetus or infant, and this decision must be made by the treating physician.

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.

Compared with single‑agent beta‑blockers or thiazide diuretics, the combination offers dual mechanisms—beta‑blockade and diuresis—in a single tablet, which can improve adherence and provide more consistent blood‑pressure control for patients needing both actions.

Store the tablets at ambient temperature, below 25 °C, in the original container to protect them from moisture and light. 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, as directed by the prescriber. Swallow the tablet whole with a glass of water; do not crush or chew it unless specifically instructed.

Serious adverse events may include severe hypotension, bradycardia, acute kidney injury, electrolyte disturbances such as hyponatraemia or hypokalaemia, and rare allergic reactions. Patients should seek immediate medical attention if they experience fainting, rapid weight gain, swelling, or signs of an allergic response.

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 heart block, or uncontrolled heart failure. It should also be avoided in individuals with anuria.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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