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

Nebivolol/Hydrochlorothiazide Cristers

Active Ingredient:
Hydrochlorothiazide, Nebivolol
Origin:
EU

Nebivolol/Hydrochlorothiazide Cristers (Hydrochlorothiazide, Nebivolol)

Nebivolol/Hydrochlorothiazide, the active ingredient in Nebivolol/Hydrochlorothiazide Cristers, is a beta‑blocker and thiazide diuretic presented as a tablet for oral use. It is prescribed to manage essential hypertension in adult patients. By combining a selective β1‑adrenergic blocker with a diuretic, the formulation helps lower blood pressure through complementary mechanisms.

GNH India supplies Nebivolol/Hydrochlorothiazide Cristers as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Cristers

1
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Indications & Clinical Uses

Nebivolol/Hydrochlorothiazide is indicated for conditions related to elevated blood pressure.

  • Essential hypertension: lowers systolic and diastolic blood pressure in adult patients.
  • Hypertension: provides combined β1‑blockade and diuretic effect to achieve target blood pressure.
  • High blood pressure requiring combined therapy: simplifies treatment by addressing cardiac output and fluid volume simultaneously.

How It Works

  • Nebivolol selectively blocks β1‑adrenergic receptors, reducing heart rate and myocardial contractility, while also enhancing nitric oxide release to promote vasodilation. Hydrochlorothiazide inhibits Na⁺/Cl⁻ reabsorption in the distal convoluted tubule, increasing urinary sodium and water excretion, which decreases plasma volume and peripheral resistance, together resulting in lowered arterial pressure.

Side Effects

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

Common Side Effects

  • Dizziness: transient light‑headedness, especially after standing.
  • Headache: mild to moderate intensity.
  • Fatigue: general tiredness or reduced energy.
  • Increased urination: due to the diuretic component.
  • Electrolyte imbalance: mild changes in potassium or sodium levels.
  • Cough: occasional dry throat irritation.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure leading to fainting.
  • Acute renal impairment: sudden decrease in kidney function.
  • Hyperuricemia or gout attacks: elevated uric acid levels.
  • Allergic reactions: rash, itching, or swelling.
  • Pancreatitis: abdominal pain with nausea.
  • Stevens‑Johnson syndrome: severe skin blistering.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety measures.

  • Monitor blood pressure: ensure adequate control without excessive drop.
  • Assess renal function: check creatinine and eGFR periodically.
  • Check electrolytes: especially potassium and sodium levels.
  • Use caution in asthma: β‑blockade may exacerbate bronchospasm.
  • Avoid abrupt discontinuation: taper to prevent rebound hypertension.
  • Store at room temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Nebivolol/Hydrochlorothiazide can interact with other medicines, requiring attention to the interaction strength.

Major Interactions (Avoid)

  • Other antihypertensives: risk of additive hypotension.
  • NSAIDs: may reduce diuretic efficacy and impair renal function.
  • Lithium: increased lithium levels leading to toxicity.
  • CYP2D6 inhibitors: elevate nebivolol plasma concentrations.
  • Potassium‑sparing diuretics: risk of hyperkalemia.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: enhanced renal effects, monitor kidney function.
  • Other beta‑blockers: additive cardiac depression.
  • Antidiabetic agents: possible hypoglycemia, monitor glucose.
  • Antidepressants (SSRIs): may affect blood pressure control.
  • Anticoagulants: monitor for bleeding risk due to potential platelet effects.

Frequently Asked Questions

Nebivolol/Hydrochlorothiazide is prescribed to treat essential hypertension. The combination lowers blood pressure by reducing heart rate and cardiac output through nebivolol, while hydrochlorothiazide decreases fluid volume via diuresis, offering a dual approach for adult patients with high blood pressure.

Nebivolol selectively blocks β1‑adrenergic receptors in the heart, decreasing heart rate and contractility. It also stimulates nitric oxide release from the endothelium, causing vasodilation. This dual action reduces cardiac workload and peripheral resistance, contributing to lower blood pressure.

The specific dose of Nebivolol/Hydrochlorothiazide is determined by the prescribing clinician based on the patient’s medical condition, response to therapy, and other individual factors. Patients should follow the dosage instructions provided by their healthcare professional.

Safety information for Nebivolol/Hydrochlorothiazide in pregnancy and lactation is limited. Healthcare providers should evaluate the potential benefits against possible risks before prescribing to pregnant or nursing women, and alternative treatments may be considered when appropriate.

To place an order, submit an enquiry on the product page at gnhindia.com, indicating 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 therapies, the nebivolol/hydrochlorothiazide combination offers both β1‑blockade and diuretic action in one tablet, potentially improving adherence and providing synergistic blood‑pressure reduction. It may be preferred when patients need both heart‑rate control and volume reduction, whereas other classes target only one mechanism.

Nebivolol/Hydrochlorothiazide tablets should be stored at room temperature, below 25 °C, in the original packaging to protect from moisture and light. Keep the product out of reach of children and do not use if the packaging is damaged.

The medication is taken orally, usually once daily, with or without food, as directed by a healthcare professional. Patients should swallow the tablet whole with a glass of water and avoid crushing or chewing unless specifically instructed.

Serious risks include severe hypotension, acute kidney injury, significant electrolyte disturbances (such as hyperkalemia or hyponatremia), and rare allergic reactions like Stevens‑Johnson syndrome. Patients should seek immediate medical attention if they experience fainting, rapid weight gain, swelling, or severe skin rash.

Nebivolol/Hydrochlorothiazide is contraindicated in patients with known hypersensitivity to either component, severe bradycardia, advanced heart block without a pacemaker, or those with severe renal impairment. Caution is also advised for individuals with asthma, uncontrolled diabetes, or electrolyte disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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