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 thiazide diuretic and β1‑selective blocker combination presented as an oral tablet for oral use. The product is indicated for the treatment of hypertension in adult patients, helping to lower elevated blood pressure and reduce cardiovascular risk.

GNH India supplies Nobiretic as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, adhering to stringent quality standards and providing reliable global distribution, ensuring product integrity throughout the supply chain.

Manufacturer / TM Owner

Menarini International Operations Luxembourg S.A.

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Indications & Clinical Uses

Nobiretic, a combined thiazide diuretic and β1‑selective blocker, is used in the management of high blood pressure.

  • Essential hypertension: reduces systolic and diastolic pressure to target levels.
  • Secondary hypertension: assists in controlling blood pressure when caused by renal or endocrine disorders.
  • Hypertension with concomitant heart failure: helps lower pressure while providing β‑blockade benefits.

How It Works

  • Hydrochlorothiazide inhibits sodium and chloride reabsorption in the distal convoluted tubule, increasing urinary excretion of water and electrolytes, which lowers plasma volume. Nebivolol selectively blocks β1‑adrenergic receptors, decreasing heart rate and contractility, while also stimulating endothelial nitric‑oxide release, producing vasodilation. The combined actions reduce cardiac output and peripheral resistance, resulting in lowered arterial blood pressure.

Side Effects

Nobiretic may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Dizziness: sensation of light‑headedness, especially after standing.
  • Headache: mild to moderate pain in the head region.
  • Fatigue: feeling unusually tired or weak.
  • Increased urination: more frequent need to void.
  • Dry mouth: reduced salivary flow causing discomfort.
  • Mild gastrointestinal discomfort: nausea or abdominal upset.

Serious or Rare Side Effects

  • Severe electrolyte disturbance: abnormal potassium or sodium levels requiring medical attention.
  • Acute renal failure: sudden loss of kidney function.
  • Significant bradycardia: heart rate dropping below normal limits.
  • Hypotension: markedly low blood pressure that may cause fainting.

Precautions & Warnings

When prescribing Nobiretic, clinicians should consider several precautionary measures to ensure patient safety.

  • Monitor electrolytes: check serum potassium and sodium regularly.
  • Assess renal function: evaluate creatinine clearance before and during therapy.
  • Avoid abrupt discontinuation: taper dose to prevent rebound hypertension.
  • Caution in gout patients: diuretic component may increase uric acid levels.
  • Use with caution in severe hepatic impairment: drug metabolism may be altered.
  • Store at room temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Nobiretic can interact with other medicines, requiring careful assessment of concomitant therapy.

Major Interactions (Avoid)

  • Concurrent use with other diuretics: risk of excessive volume depletion.
  • Combined with ACE inhibitors or ARBs: may increase risk of renal dysfunction.
  • Co‑administration with potassium‑sparing agents: risk of hyperkalaemia.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may reduce antihypertensive effect.
  • Other β‑blockers or β‑agonists: may diminish nebivolol efficacy.
  • Lithium: may increase lithium serum concentrations, requiring monitoring.

Frequently Asked Questions

Nobiretic is prescribed to lower elevated blood pressure in adults. It combines a thiazide diuretic with a β1‑selective blocker to manage essential and secondary hypertension, helping to reduce the risk of cardiovascular complications.

Hydrochlorothiazide promotes the excretion of sodium and water by inhibiting reabsorption in the kidney, decreasing blood volume. Nebivolol blocks β1‑adrenergic receptors, lowering heart rate and contractility, and enhances nitric‑oxide‑mediated vasodilation. Together they lower cardiac output and peripheral resistance, resulting in reduced blood pressure.

The appropriate dose of Nobiretic is determined by the prescribing healthcare professional based on the patient’s clinical condition, response to therapy, and any concomitant medications. Dosage adjustments are made individually and should follow the prescriber’s instructions.

Safety of Nobiretic in pregnancy or while breastfeeding has not been fully established. Healthcare providers should weigh the potential benefits against possible risks and consider alternative treatments if appropriate. Patients should discuss their specific situation with a qualified clinician.

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 dual action of a thiazide diuretic and a β1‑selective blocker in one tablet, potentially simplifying regimens and improving adherence. It may be preferred when both volume reduction and β‑blockade are clinically indicated, but choice depends on individual patient factors.

Nobiretic tablets should be stored at room temperature, below 25 °C, in the original packaging to protect them from moisture and light. Keep the product out of reach of children and do not use after the expiration date.

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

Serious risks include severe electrolyte imbalances, acute kidney injury, marked hypotension, and significant bradycardia. Patients should be monitored for signs of these conditions, especially during treatment initiation or dose changes.

Nobiretic is contraindicated in patients with known hypersensitivity to either component, severe renal or hepatic impairment, and in those with certain cardiac conduction disorders. It should also be avoided in individuals taking contraindicated medications without appropriate medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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