Product image of Nefrix (Hydrochlorothiazide) supplied by GNH India

Nefrix

Active Ingredient:
Hydrochlorothiazide
Origin:
EU

Nefrix (Hydrochlorothiazide)

Hydrochlorothiazide, the active ingredient in Nefrix, is a thiazide diuretic presented as an oral tablet for oral use. It is employed to lower blood pressure and to reduce fluid accumulation in conditions such as heart failure, renal disease, and liver cirrhosis.

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

Manufacturer / TM Owner

Zentiva S.A.

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Indications & Clinical Uses

Hydrochlorothiazide acts on the renal distal convoluted tubule to manage fluid balance and vascular resistance, making it useful in several cardiovascular and renal conditions.

  • Hypertension: lowers systemic blood pressure by reducing plasma volume.
  • Edema associated with heart failure: promotes fluid excretion to relieve congestion.
  • Edema due to renal disease: assists in removing excess interstitial fluid.
  • Edema secondary to liver cirrhosis: decreases ascites and peripheral swelling.

How It Works

  • Hydrochlorothiazide inhibits the Na+/Cl- symporter in the distal convoluted tubule of the kidney, leading to increased urinary excretion of sodium, chloride, and water. This diuretic effect reduces extracellular fluid volume, decreases cardiac preload, and ultimately lowers systemic vascular resistance, contributing to blood pressure reduction.

Side Effects

Hydrochlorothiazide may cause a range of adverse reactions, from mild to severe, depending on patient factors and concomitant therapies.

Common Side Effects

  • Increased urination: more frequent or larger volume of urine.
  • Electrolyte imbalance: low potassium or sodium levels.
  • Dizziness or light‑headedness, especially upon standing.
  • Headache.
  • Fatigue.
  • Elevated blood glucose levels.

Serious or Rare Side Effects

  • Severe dehydration or hypotension.
  • Significant electrolyte disturbances such as hyponatremia or hypokalemia.
  • Gout flare due to increased uric acid.
  • Pancreatitis.
  • Allergic reactions including rash, angioedema, or anaphylaxis.
  • Blood dyscrasias such as agranulocytosis or thrombocytopenia.

Precautions & Warnings

When prescribing or dispensing Hydrochlorothiazide, clinicians should consider several safety measures.

  • Monitor electrolytes: check serum potassium, sodium, and magnesium regularly.
  • Assess renal function: evaluate creatinine and eGFR before initiation and during therapy.
  • Use cautiously in diabetes: may affect glucose control.
  • Avoid abrupt discontinuation: taper to prevent rebound hypertension.
  • Adjust dose in elderly patients: start low and monitor for orthostatic changes.
  • Store at room temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Hydrochlorothiazide can alter the pharmacokinetics or pharmacodynamics of several medicines.

Major Interactions (Avoid)

  • Lithium: increased risk of lithium toxicity.
  • NSAIDs: may blunt diuretic efficacy and affect renal function.
  • ACE inhibitors or ARBs: heightened risk of severe hypotension and renal impairment.

Moderate Interactions (Monitor Closely)

  • Digoxin: low potassium can increase digoxin toxicity.
  • Warfarin: may alter INR and bleeding risk.
  • Antidiabetic agents: enhanced hypoglycaemic effect.
  • Corticosteroids: may counteract diuretic sodium‑loss effect.

Frequently Asked Questions

Nefrix contains hydrochlorothiazide, which is prescribed to treat hypertension and to manage edema associated with heart failure, renal disease, or liver cirrhosis. By promoting the excretion of excess fluid and salts, it helps lower blood pressure and reduce swelling in these clinical settings.

Hydrochlorothiazide blocks the sodium‑chloride symporter in the distal convoluted tubule of the kidney. This inhibition leads to increased loss of sodium, chloride, and water in the urine, decreasing plasma volume and peripheral resistance, which together lower systemic blood pressure and alleviate fluid overload.

The appropriate dose of Nefrix is determined by the prescribing clinician based on the individual’s medical condition, response to therapy, and renal function. Dosage adjustments are made according to clinical guidelines and patient-specific factors.

The safety of hydrochlorothiazide in pregnancy and lactation has not been definitively established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made 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.

Nefrix (hydrochlorothiazide) belongs to the thiazide diuretic class, which reduces blood pressure primarily by decreasing fluid volume. Compared with calcium‑channel blockers or ACE inhibitors, thiazides are often used as first‑line agents, especially in combination therapy, due to their efficacy, low cost, and well‑characterized safety profile.

Nefrix should be stored at room temperature, below 25 °C. Keep the tablets in the original packaging, protect them from moisture and direct sunlight, and ensure they are out of reach of children.

Nefrix is taken orally, usually with a full glass of water. It can be taken with or without food, but patients should follow the prescribing physician’s instructions regarding timing and any dietary considerations.

Serious risks include severe dehydration, marked electrolyte disturbances such as hyponatremia or hypokalemia, gout attacks, and rare allergic reactions like angioedema. Patients should be monitored for signs of these conditions, especially during the initial weeks of therapy.

Nefrix is contraindicated in patients with known hypersensitivity to hydrochlorothiazide or other sulfonamide-derived drugs, severe renal impairment, anuria, or those who are unable to maintain adequate fluid and electrolyte balance. Clinicians should evaluate each patient’s medical history before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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