DrugInfoSys

Digoxin

Also known as: Digitek.

Drug #241

Medicinal plants containing cardiac glycosides were known to the ancient Egyptians 3000 years ago, but these agents were used randomly and with variable success until the 18th century, when William Withering an English physician and botanist, published a monograph describing the clinical effects of an extract of the foxglove plant i.e., Digitalis purpurea in 1785, described in detail the indication for use of cardiacglycoside. Digoxin is considered as a prototype cardiac glycoside, combine a steroid nucleus with an unsaturated five membered lactone ring at the 17th position and a series of sugar linked to carbon 3 of nucleus, containing 3 molecules of digitxose linked to digitoxigenin. Digoxin is obtained from the leaves of Digitalis lanata. It makes the heart function more efficient. It increases the force of contraction of heart and slows heart rate, used to treat congestive heart failure, to control ventricular rate in the treatment of supraventricular dysrhythmias including atrial fibrillation and flutter, and to treat paroxysmal atrial tachycardia. Digoxin - specific antibody fragments are used FOR the treatment of known or strongly suspected, life - threatening digoxin or digitoxin overdosage, where measures beyond the discontinuation of digoxin or digitoxin and correction of electrolyte abnormality are felt to be necessary.

Primary Characteristics

Digoxin is also known as Digitek..

It is of Natural origin and belongs to Glycosides.

It belongs to Sodium Potassium atpase inhibitor pharmacological group on the basis of mechanism of action and also classified in Anti arrhythmic agents pharmacological group. It is also classified under Cardiac Glycosides .

Molecular Weight: 780.9 · pKa: unionized · Solubility in Water: insoluble · Solubility in Alcohol: 1 in 122 (slightly soluble) · Non-proprietary name: Digoxin.

Molecular structure of Digoxin

Pharmacokinetics

Absorption: Digoxin has an oral bioavailability is 95% (±5%), pre-systemic (first-pass) metabolism accounts for 67.5% (±17.5%).

Distribution: Digoxin has a volume of distribution is 6-7l/kg. plasma protein binding is 20-30%.

Elimination: it is metabolised via 10-20%hepatic, plasma half-life is 36-41hrs or 1.5-2 days, renal excretion is 60-90%.

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Indications

Contraindications

Dosage

Digoxin's dosage details are as follows:

DoseSingle DoseFrequencyRouteInstructions
Adult Dosage
25 ug/kg25 ug/kgFor 5-10 years
35 ug/kg35 ug/kg2-5 years
187.5 ug187.5 ugEvery 24hPOMaintenance, As Required
1125 ug1125 ugEvery 6hPOIn div.doses.
Paediatric Dosage (20kg)
3.75 ug/kg3.75 ug/kgEvery 12hIntra MuscularMaintenance (25% of loading dose)
30 ug/kg30 ug/kgIntra MusularInitially As Required
3.75 ug/kg3.75 ug/kgEvery 12hIntra VenousMaintenance (25% of loading dose)
30 ug/kg30 ug/kgIntra Venous Initially As Required
4.375 ug/kg4.375 ug/kgEvery 12hOralMaintenance (25% of loading dose)
35 ug/kg35 ug/kgOral Initially, As Required
Neonatal Dosage (3kg)
6.25 mg/kg6.25 mg/kgEvery 12horalMaintenance, As required
47.5 ug/kg47.5 ug/kgoralInitial dose, As required

Drug Interactions

Unknown43 interactions
38 interactions
Major4 interactions
Minor5 interactions
Moderate46 interactions
N/A1 interaction

Always consult your physician for the change of dose regimen or an alternative drug of choice that may strictly be required.

Side Effects

Digoxin in overdosage may give rise to further complications which include Ventricular tachycardia , Ventricular fibrillation , Supraventricular extra beats , Heart block , Rhodopsia , Cyanopsia, Castanopsia , Melanopsin, Increased FSH (follicular stimulating hormone), Increased estrogen, Decreased LH, Decreased testosterone , Color vision disturbance.

Digoxin produces potentially life-threatening effects which include Cardiac arrhythmias, Heart block. Careful monitoring is needed with proper medical management.

The signs and symptoms that are produced after acute overdosage of Digoxin are Ventricular arrhythmias, Heart block, Hyperkalemia.

Digoxin is known to cause more or less tolerable side effects which are usually transient. These include Agitation , Anorexia , dizziness, Drowsiness, ECG changes, Gynecomastia, Nausea, Nervousness, Potassium depletion, PR interval prolongation, Restlessness, Skin lesion, Thrombocytopenia, Vomiting .

Warnings / Precautions

Digoxin should be used with caution in patients with any allergy, especially drug allergies, heart, lung or kidney diseases, high blood pressure, hypothyroidism or low potassium levels. Limit alcohol intake (e.g.certain liquid medications containing alcohol) since the side effects of this medication may be increased by alcohol. This medication should be used only when clearly needed during pregnancy or lactation. Caution is advised when this drug is used in the elderly.

Interference in Pathology

Digoxin may interfere in the diagnosis of Increase apparent conc. of 17-OH Corticosteroids in the Urine. .

Available Brands

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Single Ingredient

Storage Conditions

Digoxin should be stored . Inj. Tab, Syrup.

Drug Classification

  1. 1.4.2.11Miscellaneous
  2. 2.12.2Antiarrhythmic drugs
  3. 3.12.4Drugs used in heart failure

Manufacturers

Manufacturers of Digoxin in Pakistan: