Product image of Orgaran (Danaparoid Sodium) supplied by GNH India

Orgaran

Active Ingredient:
Danaparoid Sodium
Origin:
EU

Orgaran (Danaparoid Sodium)

Danaparoid Sodium, the active ingredient in Orgaran, is a Heparinoid (Anticoagulant) presented as an unknown/unknown for intravenous use. It is used to prevent and treat venous thromboembolism and to manage heparin‑induced thrombocytopenia in adult patients.
GNH India supplies Orgaran as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and clinics worldwide.

Manufacturer / TM Owner

Viatris Oy

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Indications & Clinical Uses

Orgaran is a heparinoid anticoagulant that acts on the coagulation cascade to reduce clot formation.

  • Deep vein thrombosis: prevents clot propagation and facilitates resolution in at‑risk patients.
  • Pulmonary embolism: reduces the size of existing emboli and prevents new clot formation in the pulmonary arteries.
  • Heparin‑induced thrombocytopenia (HIT): provides an alternative anticoagulant option when heparin therapy is contraindicated.

How It Works

  • Danaparoid Sodium exerts its antithrombotic effect by indirectly inhibiting factor Xa. It enhances the activity of antithrombin III and heparin cofactor II, leading to reduced conversion of prothrombin to thrombin and consequently decreasing fibrin clot formation.

Side Effects

Adverse reactions may occur with any anticoagulant therapy.

Common Side Effects

  • Minor bleeding at injection site: mild bruising or oozing.
  • Gastrointestinal upset: nausea or abdominal discomfort.
  • Elevated liver enzymes: transient increase in hepatic transaminases.
  • Rash or mild skin irritation: localized erythema.

Serious or Rare Side Effects

  • Major hemorrhage: life‑threatening internal bleeding.
  • Thrombocytopenia: significant drop in platelet count unrelated to HIT.
  • Anaphylactic reaction: severe hypersensitivity requiring immediate medical intervention.

Precautions & Warnings

Use Orgaran only under careful clinical supervision and after evaluating individual risk factors.

  • Renal impairment: monitor renal function and adjust therapy as needed.
  • Bleeding risk: assess patient history of bleeding disorders before initiation.
  • History of HIT: contraindicated in patients with prior heparin‑induced thrombocytopenia.
  • Concurrent anticoagulants: avoid combination with other anticoagulant agents unless specifically directed.
  • Pregnancy: consider only if potential benefits outweigh risks to the fetus.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Co‑administration with certain drugs can alter anticoagulant effect.

Major Interactions (Avoid)

  • Direct thrombin inhibitors (e.g., dabigatran): may cause uncontrolled bleeding.
  • High‑dose aspirin or other antiplatelet agents: significantly increase hemorrhagic risk.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may potentiate bleeding tendency.
  • Certain antibiotics (e.g., quinolones): can affect platelet function.
  • Vitamin K antagonists (e.g., warfarin): may require dose adjustments and close INR monitoring.

Frequently Asked Questions

Orgaran is an injectable anticoagulant containing Danaparoid Sodium. It is indicated for the prevention and treatment of venous thromboembolism, such as deep vein thrombosis and pulmonary embolism, and for managing heparin‑induced thrombocytopenia in patients who cannot receive heparin.

Danaparoid Sodium works by indirectly inhibiting factor Xa. It enhances the activity of antithrombin III and heparin cofactor II, which together reduce the conversion of prothrombin to thrombin, thereby decreasing fibrin clot formation and limiting thrombus growth.

The dosage of Orgaran is individualized. The prescribing clinician determines the appropriate dose, infusion rate, and treatment duration based on the patient’s clinical condition, weight, renal function, and response to therapy.

Safety data for Danaparoid Sodium in pregnancy and lactation are limited. It should be used only if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by the treating physician.

To request Orgaran, 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 any cold‑chain requirements), and necessary import documentation.

Orgaran (Danaparoid Sodium) differs from heparin and low‑molecular‑weight heparins by having a lower risk of inducing HIT. Its indirect factor Xa inhibition provides effective anticoagulation while offering an alternative for patients who have experienced heparin‑related complications.

Orgaran should be stored at ambient temperature, protected from light and moisture, and kept in its original packaging until use. Do not freeze the product, and ensure the vial is inspected for particulate matter before administration.

Orgaran is administered intravenously by a healthcare professional. The solution is typically infused over a prescribed period, with dosing adjustments made according to laboratory monitoring of coagulation parameters and the patient’s clinical response.

The most serious risks include major hemorrhage, severe allergic reactions such as anaphylaxis, and rare cases of thrombocytopenia unrelated to HIT. Patients should be closely monitored for signs of uncontrolled bleeding or hypersensitivity during therapy.

Orgaran is contraindicated in patients with a known hypersensitivity to Danaparoid Sodium or any component of the formulation, in those with active major bleeding, and in individuals with a documented history of heparin‑induced thrombocytopenia.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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