Product image of Hemigoxine Nativelle (Digoxin) supplied by GNH India

Hemigoxine Nativelle

Active Ingredient:
Digoxin
Origin:
EU

Hemigoxine Nativelle (Digoxin)

Hemigoxine Nativelle is a prescription oral medication that contains the cardiac glycoside digoxin. It is marketed in the European Union and is supplied as a tablet (strength not specified). Digoxin works by inhibiting the Na+/K+ ATPase pump, which increases intracellular calcium and enhances cardiac contractility while slowing atrioventricular nodal conduction.

Manufacturer / TM Owner

Teofarma S.R.L.

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Indications & Clinical Uses

Hemigoxine Nativelle is indicated for the management of certain heart conditions where improved cardiac output and rhythm control are needed.

  • Treatment of chronic heart failure to improve symptoms and exercise tolerance.
  • Rate control in patients with atrial fibrillation or atrial flutter.
  • Adjunct therapy in patients with congestive cardiomyopathy.
  • Use in selected cases of supraventricular tachycardia when other agents are unsuitable.
  • May be employed in palliative care to alleviate dyspnea related to cardiac dysfunction.

Side Effects

Side effects of digoxin can vary in frequency and severity.

Common

  • Nausea or vomiting
  • Diarrhea or abdominal cramps
  • Fatigue or weakness
  • Visual disturbances such as blurred vision or yellow‑green halos
  • Dizziness or headache

Serious

  • Cardiac arrhythmias (e.g., premature ventricular beats, atrioventricular block)
  • Severe bradycardia
  • Confusion, delirium, or hallucinations
  • Hyperkalemia or electrolyte imbalance leading to toxicity
  • Life‑threatening heart block

Precautions & Warnings

Before initiating Hemigoxine Nativelle, clinicians should evaluate several safety factors.

  • Assess renal function and adjust dose in patients with impaired clearance.
  • Monitor serum digoxin levels, electrolytes (especially potassium and magnesium), and thyroid function regularly.
  • Use caution in patients with pre‑existing conduction disorders or bradycardia.
  • Pregnancy category C: weigh potential benefits against risks; avoid use in the first trimester if possible.
  • Elderly patients may be more susceptible to toxicity; start at lower doses.
  • Discontinue or adjust dose before surgery or procedures that may affect fluid balance.

Avoid Interactions

Digoxin interacts with a range of medications that can alter its concentration or cardiac effects.

Avoid

  • Strong P‑glycoprotein inhibitors (e.g., amiodarone, quinidine, verapamil) that increase digoxin levels.
  • Diuretics that cause hypokalemia or hypomagnesemia (e.g., furosemide) which predispose to toxicity.
  • Certain antibiotics (e.g., erythromycin, clarithromycin) that raise serum digoxin.
  • Antifungal agents like itraconazole that inhibit metabolism.

Use with caution

  • Beta‑blockers and calcium channel blockers that may enhance AV‑node slowing.
  • Antithyroid drugs or levothyroxine, as thyroid status influences digoxin sensitivity.
  • NSAIDs that may reduce renal clearance.
  • St. John’s wort, a P‑glycoprotein inducer, which can lower digoxin concentrations.

Frequently Asked Questions

Hemigoxine Nativelle contains digoxin, which inhibits the Na+/K+ ATPase pump, leading to increased intracellular calcium and a positive inotropic effect while slowing atrioventricular nodal conduction.

It is commonly prescribed for chronic heart failure to improve symptoms and for rate control in atrial fibrillation or atrial flutter.

Renal impairment reduces digoxin clearance, so dose adjustments and close monitoring of serum levels are recommended in patients with decreased kidney function.

Regular monitoring of serum digoxin concentration, electrolytes (especially potassium and magnesium), renal function, and thyroid function is advised.

It is classified as pregnancy category C; it should only be used when the potential benefits justify the potential risks to the fetus, and preferably avoided in the first trimester.

Common gastrointestinal side effects include nausea, vomiting, diarrhea, and abdominal cramps.

Patients may experience blurred vision, yellow‑green halos around lights, or decreased visual acuity, which can be signs of digoxin toxicity.

Serious toxicity can lead to premature ventricular contractions, atrioventricular block, and severe bradycardia.

Strong P‑glycoprotein inhibitors such as amiodarone, quinidine, verapamil, certain macrolide antibiotics, and some antifungal agents should be avoided.

Loop diuretics can cause hypokalemia or hypomagnesemia, which increase the risk of digoxin toxicity; electrolyte levels should be monitored and corrected.

Elderly patients are more prone to toxicity; starting at a lower dose and careful monitoring is recommended.

The dose may need to be reduced or temporarily discontinued before surgery, especially if fluid shifts or electrolyte changes are expected.

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GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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