Arixtra (Fondaparinux)

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Brand Name : Arixtra

Marketing Authorization Holder : Aspen

Prescription Required

 
 
No Generic Medicine available for this medicine.

Product Details

Arixtra

Information about Arixtra (Fondaparinux)

Arixtra, which contains the active ingredient fondaparinux, is an anticoagulant used to prevent and treat blood clots. It’s commonly prescribed for:

  • Deep Vein Thrombosis (DVT): To prevent and treat blood clots in the deep veins, typically following surgeries or for individuals who are bedridden.
  • Pulmonary Embolism (PE): To manage and prevent blood clots in the lungs.
  • Acute Coronary Syndrome (ACS): As part of the treatment for unstable angina and non-ST elevation myocardial infarction (NSTEMI) to prevent clot formation.
  • Post-surgical prophylaxis: To prevent DVT and PE in patients undergoing certain types of surgery.

Product Highlights

  • Arixtra belong to medicine group Fondaparinux is classified as a synthetic pentasaccharide anticoagulant.
  • It is administered via subcutaneous injection.
  • It has a relatively long half-life and provides sustained anticoagulation with once-daily dosing.
  • Unlike some other anticoagulants, it typically doesn’t require routine monitoring of blood levels.

Key Ingredients

  • Fondaparinux Sodium
  • Sodium Chloride
  • Water for Injection

Key Benefits

  • Provides effective prevention and treatment of blood clots.
  • Compared to other anticoagulants, fondaparinux has a lower risk of major bleeding complications.
  • Administered once daily, this improves patient compliance.
  • It has a predictable effect, minimizing the need for frequent monitoring.

Direction For Use

  • The dose depends on the condition being treated. For example, the typical dose for DVT or PE is 2.5 mg once daily.
  • It is a subcutaneous injection in the abdomen.
  • Rotate injection sites to minimize irritation and tissue damage. Don’t massage the injection site after injection taken.

Safety Concern

  • As with all anticoagulants, there is a risk of bleeding. Patients should be monitored for signs of bleeding and have regular medical follow-ups.
  • Dose adjustments may be necessary for patients with impaired renal function, as the drug is primarily eliminated through the kidneys.
  • Safety during pregnancy and breastfeeding is not well established; it should be used only if the potential benefit justifies the risk.

Avoid Arixtra (Fondaparinux) If

  • Patients with severe renal impairment should avoid using Arixtra due to the risk of accumulation and bleeding complications.
  • Individuals with active bleeding conditions or a history of major bleeding disorders should not use Arixtra.
  • Those with a known hypersensitivity to fondaparinux or any components of the formulation should avoid using this medication.
  • Patients with a low platelet count (thrombocytopenia) or a history of heparin-induced thrombocytopenia should avoid Arixtra due to the increased risk of adverse effects.

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