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Enifrav

Active Ingredient:
Warfarin Sodium
Origin:
EU

Enifrav (Warfarin Sodium)

Enifrav is a prescription medication containing warfarin sodium as its active ingredient, provided in an oral dosage form with strength not specified on the label. It belongs to the anticoagulant class of drugs, specifically vitamin K antagonists, and is marketed in the European Union. It is used under medical supervision to reduce the risk of blood clots in various cardiovascular conditions. Patients should follow regular monitoring.

Manufacturer / TM Owner

A.Forall Development Nv

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Indications & Clinical Uses

Enifrav is indicated for several thromboembolic disorders where anticoagulation is required.

  • Prevention and treatment of venous thromboembolism (deep‑vein thrombosis and pulmonary embolism).
  • Prophylaxis of stroke and systemic embolism in patients with non‑valvular atrial fibrillation.
  • Prevention of thromboembolic complications in individuals with mechanical heart valve prostheses.
  • Long‑term anticoagulation in patients with recurrent clotting disorders as determined by a physician.

Side Effects

Side effects of Enifrav vary in frequency and severity; they are categorized as common and serious.

Common

  • Minor bruising or bleeding from gums, nose, or cuts.
  • Small amounts of blood in urine or stool.
  • Nausea, abdominal discomfort, or loss of appetite.
  • Skin rash or mild itching.
  • Dizziness or light‑headedness.

Serious

  • Significant bleeding such as gastrointestinal hemorrhage or intracranial bleed.
  • Severe allergic reaction with swelling of the face, lips, or throat.
  • Unexplained drop in hemoglobin or hematocrit levels.
  • Purple or black discoloration of the skin (purpura).
  • Rapid drop in blood pressure (hypotension) due to bleeding.

Precautions & Warnings

Before initiating Enifrav, clinicians evaluate several precautionary factors to minimize bleeding risk and ensure safe use.

  • Baseline assessment of INR or PT/INR values and regular monitoring during therapy.
  • Evaluation of liver function, as impaired hepatic metabolism can increase drug exposure.
  • Review of patient history for prior hemorrhagic events, gastrointestinal ulcers, or intracranial bleeding.
  • Consideration of age, renal function, and concomitant use of antiplatelet agents.
  • Education on signs of bleeding and instructions to avoid activities that may cause trauma.
  • Pregnancy and lactation status should be assessed, as warfarin crosses the placenta.

Avoid Interactions

Enifrav interacts with many medications; some combinations should be avoided, while others require careful dose adjustment and monitoring.

Avoid

  • Strong CYP2C9 inhibitors such as fluconazole, amiodarone, and certain macrolide antibiotics.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) and aspirin that increase bleeding risk.
  • Antiplatelet agents like clopidogrel or ticagrelor without close supervision.

Use with caution

  • Vitamin K‑rich foods or supplements that may reduce anticoagulant effect.
  • Other anticoagulants (e.g., heparin, direct oral anticoagulants) when transitioning therapy.
  • Herbal products such as ginkgo biloba, garlic, or St. John’s wort that can affect coagulation.

Frequently Asked Questions

Enifrav contains warfarin sodium, which is a vitamin K antagonist used as an oral anticoagulant.

Enifrav is prescribed for prevention and treatment of venous thromboembolism, stroke prophylaxis in atrial fibrillation, and to prevent clotting in patients with mechanical heart valves.

Enifrav inhibits vitamin K epoxide reductase, reducing the synthesis of vitamin K‑dependent clotting factors II, VII, IX, and X, which decreases the blood’s ability to form clots.

No, Enifrav is a prescription‑only medication and must be prescribed by a qualified healthcare professional.

Patients on Enifrav require regular monitoring of their INR (International Normalized Ratio) or PT/INR to ensure therapeutic anticoagulation and to adjust the dose as needed.

Vitamin K supplements can reduce the anticoagulant effect of Enifrav; they should only be used under medical supervision and with careful INR monitoring.

Common side effects include minor bruising, nosebleeds, gum bleeding, small amounts of blood in urine or stool, nausea, abdominal discomfort, skin rash, and dizziness.

Serious events include significant bleeding such as gastrointestinal hemorrhage or intracranial bleed, severe allergic reactions with facial swelling, sudden drop in hemoglobin, purpura, or rapid drop in blood pressure.

Foods high in vitamin K, such as leafy green vegetables, can affect the drug’s effectiveness. Consistency in dietary vitamin K intake is recommended, and any major changes should be discussed with a healthcare provider.

Yes, herbal products like ginkgo biloba, garlic, and St. John’s wort can increase bleeding risk or alter anticoagulation and should be used only after consulting a physician.

Warfarin crosses the placenta and may cause fetal harm; its use during pregnancy is generally avoided unless the benefits outweigh the risks and is managed by a specialist.

If a dose is missed, take it as soon as you remember unless it is near the time of the next scheduled dose. Do not double‑dose; contact your healthcare provider for guidance.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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