Product image of Lanoxin (Digoxin) supplied by GNH India

Lanoxin

Active Ingredient:
Digoxin
Origin:
EU

Lanoxin (Digoxin)

Digoxin, the active ingredient in Lanoxin, is a cardiac glycoside presented as an injectable solution for intravenous use. It is employed to improve cardiac contractility in heart failure and to achieve rate control in atrial fibrillation, mainly in adult patients.

GNH India supplies Lanoxin as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation for cross‑border distribution, ensuring product integrity throughout the supply chain.

Manufacturer / TM Owner

Aspen Pharma Trading Limited

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Indications & Clinical Uses

  • Digoxin is a cardiac glycoside used in the management of heart failure and atrial arrhythmias.
  • Heart failure: improves ventricular contractility and reduces symptoms of fluid overload.
  • Atrial fibrillation (rate control): slows atrioventricular conduction to maintain an appropriate ventricular rate.
  • Atrial flutter (rate control): reduces ventricular response by decreasing AV nodal conduction.

How It Works

  • Digoxin binds to and inhibits the Na⁺/K⁺‑ATPase pump on cardiac myocyte membranes, leading to an increase in intracellular sodium. This alteration reduces the activity of the sodium‑calcium exchanger, causing calcium accumulation inside the cells, which enhances contractile force (positive inotropy) and prolongs the refractory period of the AV node, thereby slowing ventricular rate.

Side Effects

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Vomiting: occasional emesis, especially with rapid infusion.
  • Diarrhea: loose stools may occur.
  • Blurred vision: transient visual disturbances, such as yellow‑green halos.

Serious or Rare Side Effects

  • Life‑threatening arrhythmias: ventricular tachycardia or fibrillation.
  • Severe bradycardia: markedly reduced heart rate.
  • Heart block: advanced AV conduction delay.
  • Allergic skin reactions: rash, urticaria, or angioedema.

Precautions & Warnings

Before initiating therapy, consider the following precautions:

  • Renal function: adjust dose in patients with impaired clearance.
  • Electrolytes: monitor potassium and magnesium levels to avoid toxicity.
  • Cardiac monitoring: obtain baseline and periodic ECGs for arrhythmia detection.
  • Pregnancy: use only if the potential benefit justifies the potential risk (Category C).
  • Breastfeeding: assess risk versus benefit, as digoxin is excreted in milk.

Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Digoxin has several clinically important drug interactions.

Major Interactions (Avoid)

  • Amiodarone: markedly increases digoxin serum concentrations.
  • Quinidine: can precipitate digoxin toxicity.
  • Dronedarone: may raise digoxin levels and risk of arrhythmias.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: additive effects on heart rate and AV conduction.
  • Diuretics causing hypokalemia: low potassium enhances digoxin toxicity.
  • ACE inhibitors or ARBs: may increase serum digoxin through reduced renal clearance.

Frequently Asked Questions

Lanoxin contains digoxin, which is indicated for the treatment of chronic heart failure to improve cardiac output and for rate control in atrial fibrillation. It helps reduce symptoms such as shortness of breath and limits rapid ventricular response in atrial arrhythmias.

Digoxin inhibits the Na⁺/K⁺‑ATPase pump on heart muscle cells, leading to increased intracellular sodium. This change reduces the activity of the sodium‑calcium exchanger, causing calcium buildup that strengthens heart contractions and prolongs AV‑node refractory period, thereby slowing ventricular rate.

The dose of Lanoxin is individualized and determined by the prescribing clinician based on the patient’s age, renal function, electrolyte status, and therapeutic response. Dosing regimens are adjusted to achieve target serum digoxin concentrations while minimizing toxicity.

Lanoxin is classified as Pregnancy Category C, meaning risk cannot be ruled out. It should be used only when the potential maternal benefit justifies potential fetal risk. Digoxin is excreted in breast milk; breastfeeding decisions should be made after weighing benefits and possible infant exposure.

To order Lanoxin, 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 (including cold‑chain if needed), and import documentation.

The primary alternative for rate control in atrial fibrillation is beta‑blockers, which act by reducing sympathetic stimulation. Unlike beta‑blockers, digoxin primarily enhances vagal tone and provides positive inotropy, making it useful in patients with concurrent heart failure where beta‑blockers alone may be insufficient.

Lanoxin must be stored at 2‑8 °C in a refrigerator, protected from light. The solution should not be frozen or shaken. Before use, inspect the vial for particulate matter and ensure the container remains sealed to maintain sterility.

Lanoxin is given by intravenous injection or infusion. The medication is administered slowly, typically over several minutes, under continuous cardiac monitoring to observe for arrhythmias or changes in heart rate. Administration should follow the prescriber’s specific instructions and institutional protocols.

The most critical risks include life‑threatening cardiac arrhythmias such as ventricular tachycardia, severe bradycardia, and various degrees of heart block. Early signs of digoxin toxicity—nausea, visual disturbances, and electrolyte imbalances—should prompt immediate medical evaluation.

Lanoxin is contraindicated in patients with ventricular fibrillation, known hypersensitivity to digoxin or other cardiac glycosides, and in those with uncontrolled atrial flutter or fibrillation where rapid ventricular response is required. Caution is also advised in patients with severe conduction disorders without a pacemaker.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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