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

Nebivololo E Idroclorotiazide Doc Generici

Active Ingredient:
Hydrochlorothiazide, Nebivolol
Origin:
EU

Nebivololo E Idroclorotiazide Doc Generici (Hydrochlorothiazide, Nebivolol)

Nebivolol/Hydrochlorothiazide, the active ingredient in Nebivololo E Idroclorotiazide Doc Generici, is a beta blocker and thiazide diuretic presented as a tablet for oral use. It treats hypertension in adult patients.

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

Manufacturer / TM Owner

Doc Generici S.R.L.

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Indications & Clinical Uses

Nebivolol/Hydrochlorothiazide is indicated for the management of hypertension, a condition characterized by elevated arterial pressure.

  • Hypertension: lowers systolic and diastolic blood pressure and reduces cardiovascular risk.
  • Primary (essential) hypertension: provides effective control when monotherapy is insufficient.
  • Combination therapy in adults: offers a convenient single‑tablet option for patients requiring both a beta blocker and a thiazide diuretic.

How It Works

  • Nebivolol selectively blocks β1‑adrenergic receptors, reducing heart rate and contractility, while also enhancing nitric‑oxide release for vasodilation. Hydrochlorothiazide inhibits NaCl reabsorption in the distal convoluted tubule, promoting natriuresis and diuresis, which together decrease plasma volume and peripheral resistance, resulting in lowered blood pressure.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Headache: mild to moderate pain often transient.
  • Dizziness: sensation of light‑headedness, especially on standing.
  • Fatigue: generalized tiredness.
  • Cough: dry or productive.
  • Nausea: mild stomach upset.
  • Increased urination: due to diuretic action.

Serious or Rare Side Effects

  • Severe hypotension: markedly low blood pressure requiring medical attention.
  • Electrolyte imbalance: notably low potassium or sodium levels.
  • Gout flare: increased uric acid leading to joint pain.
  • Pancreatitis: abdominal pain with elevated enzymes.
  • Allergic reactions: rash, itching, or swelling.
  • Renal impairment: reduced kidney function.

Precautions & Warnings

Patients should be evaluated for specific risk factors before initiating therapy.

  • Monitor blood pressure: ensure target levels are achieved without excessive drop.
  • Assess electrolytes: check potassium and sodium regularly.
  • Evaluate renal function: baseline and periodic creatinine measurements.
  • Use caution in diabetes: diuretics may affect glucose control.
  • Avoid abrupt discontinuation: taper to prevent rebound hypertension.
  • Store at room temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Nebivolol/Hydrochlorothiazide may interact with several drug classes.

Major Interactions (Avoid)

  • Other antihypertensives: risk of additive hypotension.
  • Potassium‑sparing diuretics: may cause hyperkalemia.
  • NSAIDs: can diminish diuretic efficacy and affect renal function.
  • Lithium: increased lithium levels and toxicity.
  • CYP2D6 inhibitors: elevate nebivolol concentrations.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: monitor renal function and potassium.
  • Additional beta blockers: risk of excessive β‑blockade.
  • Corticosteroids: may counteract antihypertensive effect.
  • Antidiabetic agents: monitor glucose as diuretics may raise blood sugar.
  • Antidepressants (tricyclics): potential additive cardiac effects.

Frequently Asked Questions

Nebivololo E Idroclorotiazide is a fixed‑dose combination of nebivolol and hydrochlorothiazide used to lower high blood pressure in adult patients. The combination provides both β1‑adrenergic blockade and diuretic action, helping to achieve better blood‑pressure control than either component alone.

Nebivolol selectively blocks β1‑adrenergic receptors in the heart, reducing heart rate and contractility. It also stimulates endothelial nitric‑oxide release, causing vasodilation. Together these actions lower cardiac output and peripheral resistance, contributing to a reduction in blood pressure.

The specific dose of Nebivololo E Idroclorotiazide is determined by the prescribing clinician based on the patient’s clinical condition, response to therapy, and any concomitant medications. Dosage adjustments are made according to individual therapeutic needs.

Safety data for nebivolol and hydrochlorothiazide in pregnancy and lactation are limited. The product should only be used if the potential benefit justifies any potential risk to the fetus or infant, and it is generally avoided unless specifically advised by a qualified healthcare professional.

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.

Nebivolol/Hydrochlorothiazide combines a β1‑selective blocker with a thiazide diuretic, offering dual mechanisms in a single tablet. Compared with monotherapy, it can achieve greater blood‑pressure reduction and improve adherence. Alternatives may include ACE inhibitors, ARBs, or calcium‑channel blockers, each with distinct efficacy and side‑effect profiles.

Store the tablets at room temperature, below 25 °C. Keep them in the original packaging to protect from moisture and light. Do not store in humid environments such as bathrooms, and keep out of reach of children.

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

Serious risks include severe hypotension, electrolyte disturbances (especially low potassium), acute kidney injury, and rare allergic reactions such as angio‑edema. Patients should be monitored for signs of dizziness, fainting, muscle cramps, or swelling, and seek medical attention promptly if they occur.

Individuals with known hypersensitivity to nebivolol, hydrochlorothiazide, or any excipients should avoid the product. It is also contraindicated in patients with severe renal impairment, uncontrolled electrolyte abnormalities, or those taking certain interacting medications without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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