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

Nobiretic

Active Ingredient:
Hydrochlorothiazide, Nebivolol
Origin:
EU

Nobiretic (Hydrochlorothiazide, Nebivolol)

Hydrochlorothiazide and Nebivolol, the active ingredients in Nobiretic, are a combination diuretic (thiazide) and beta‑blocker presented as an oral tablet for oral use. The product is indicated for the treatment of hypertension in adult patients.
GNH India supplies Nobiretic as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Menarini International Operations Luxembourg S.A.

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Indications & Clinical Uses

Nobiretic, a combination antihypertensive, is used to manage elevated blood pressure.

  • Hypertension: lowers systolic and diastolic pressure in patients with primary hypertension.
  • Essential hypertension: helps achieve target blood pressure when monotherapy is insufficient.
  • Secondary hypertension: may be employed as part of combination therapy for hypertension secondary to renal or endocrine disorders.

How It Works

  • Hydrochlorothiazide inhibits sodium‑chloride reabsorption in the distal convoluted tubule, increasing urinary excretion of water and electrolytes, which reduces plasma volume. Nebivolol selectively blocks β1‑adrenergic receptors, decreasing heart rate and contractility, while also stimulating endothelial nitric‑oxide release, leading to vasodilation. The combined actions result in lowered systemic vascular resistance and blood pressure.

Side Effects

Common Side Effects

  • Dizziness: sensation of light‑headedness, especially after standing.
  • Headache: mild to moderate pain often occurring early in therapy.
  • Increased urination: due to the diuretic component.
  • Fatigue: general tiredness or weakness.

Serious or Rare Side Effects

  • Severe electrolyte imbalance: such as hypokalemia or hyponatremia.
  • Acute gout attacks: sudden joint pain due to uric acid changes.
  • Significant hypotension: dangerously low blood pressure.
  • Bronchospasm: airway constriction, particularly in susceptible individuals.
  • Allergic reactions: including rash, angioedema, or anaphylaxis.

Precautions & Warnings

Before initiating therapy, consider the following precautions:

  • Monitor electrolytes: regularly check serum potassium and sodium levels.
  • Assess renal function: evaluate kidney function prior to and during treatment.
  • Caution in diabetes: monitor blood glucose as the drug may affect glycemic control.
  • Avoid abrupt discontinuation: sudden stop can cause rebound hypertension.
  • Store at room temperature: keep in the original pack, protect from moisture and light.

Avoid Interactions

Nobiretic may interact with several medicines.

Major Interactions (Avoid)

  • NSAIDs: may reduce diuretic efficacy and increase renal risk.
  • Other antihypertensives: can cause excessive hypotension.
  • Lithium: increased lithium levels and toxicity.
  • Potassium‑sparing diuretics: risk of hyperkalemia.
  • CYP2D6 inhibitors: elevate nebivolol plasma concentrations.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors: enhanced renal effects, monitor kidney function.
  • Antidiabetic drugs: possible alteration of glucose control.
  • Warfarin: may affect INR, require monitoring.
  • Alcohol: can increase dizziness and hypotensive effects.
  • Antidepressants (SSRIs): may augment blood pressure lowering.

Frequently Asked Questions

Nobiretic is prescribed to lower high blood pressure in adults. It combines a thiazide diuretic with a beta‑blocker to reduce both fluid volume and vascular resistance, helping achieve target blood pressure levels and decreasing the risk of cardiovascular complications.

Hydrochlorothiazide promotes the excretion of sodium and water by blocking NaCl reabsorption in the kidney, which lowers blood volume. Nebivolol blocks β1‑adrenergic receptors, slowing heart rate and contractility, and also enhances nitric‑oxide mediated vasodilation. Together they produce a synergistic antihypertensive effect.

The specific dose of Nobiretic is determined by the prescribing clinician based on the patient’s medical condition, response to therapy, and other individual factors. Dosage adjustments are made according to blood pressure targets and tolerability.

Safety of Nobiretic in pregnancy or while nursing has not been fully established. Healthcare providers should weigh potential benefits against possible risks and consider alternative treatments if safer options are available.

To request Nobiretic, 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‑component agents, Nobiretic offers the convenience of two complementary mechanisms in one tablet, potentially improving blood pressure control and adherence. It may be preferred over separate prescriptions of a thiazide and a beta‑blocker when combination therapy is indicated.

Store Nobiretic at room temperature, below 25 °C. Keep the tablets in the original packaging, protect them from moisture and direct light, and ensure the container is tightly closed to maintain stability.

Nobiretic is taken orally, usually once daily with or without food, as directed by a healthcare professional. Swallow the tablet whole with a glass of water; do not crush or chew unless specifically instructed.

Serious risks include severe electrolyte disturbances such as hypokalemia, marked hypotension, acute gout attacks, bronchospasm in susceptible individuals, and rare allergic reactions like anaphylaxis. Patients should seek immediate medical attention if they experience symptoms such as rapid heartbeat, severe dizziness, swelling, or rash.

Nobiretic should be avoided in patients with known hypersensitivity to either component, severe renal impairment, uncontrolled heart failure, or those taking contraindicated medications that could cause dangerous interactions. Clinicians must evaluate each patient’s medical history before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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