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 presented as an injectable solution for intravenous use. It is employed to prevent and treat venous thromboembolism and to manage heparin‑induced thrombocytopenia in patients who require anticoagulation.

GNH India supplies Orgaran as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres and pharmacies worldwide. The company provides regulatory‑approved batches, ensures cold‑chain logistics for injectable products, and supports customers with documentation for import and distribution across EU and other markets.

Manufacturer / TM Owner

Viatris Austria Gmbh

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Indications & Clinical Uses

Orgaran is used in the anticoagulation pathway to treat and prevent clot‑related conditions.

  • Venous thromboembolism: prevents new clot formation and treats existing deep‑vein thrombosis or pulmonary embolism.
  • Heparin‑induced thrombocytopenia (HIT): provides effective anticoagulation when heparin therapy is contraindicated.
  • Surgical prophylaxis: reduces risk of peri‑operative thrombotic events in high‑risk orthopedic or cardiac procedures.

How It Works

  • Danaparoid Sodium exerts its anticoagulant effect by potentiating antithrombin III and heparin cofactor II, leading to selective inhibition of factor Xa. This reduces thrombin generation without markedly affecting factor IIa, resulting in decreased fibrin clot formation while preserving some platelet function. The drug’s heparinoid structure confers a predictable pharmacodynamic profile suitable for intravenous administration.

Side Effects

Adverse reactions to Orgaran may vary in frequency and severity.

Common Side Effects

  • Injection site pain or erythema
  • Mild bleeding or bruising
  • Nausea or vomiting
  • Headache
  • Transient elevation of liver enzymes
  • Fever

Serious or Rare Side Effects

  • Major hemorrhage
  • Severe thrombocytopenia
  • Anaphylactic or severe hypersensitivity reactions
  • Disseminated intravascular coagulation
  • Acute renal failure
  • Adrenal hemorrhage

Precautions & Warnings

Before initiating Orgaran therapy, clinicians should observe several precautionary measures.

  • Bleeding risk assessment: evaluate patient history for active bleeding or recent surgery.
  • Coagulation monitoring: regularly check activated partial thromboplastin time or anti‑Xa levels.
  • Renal function evaluation: adjust use in patients with impaired kidney function.
  • History of HIT: confirm diagnosis before selecting Danaparoid.
  • Concomitant anticoagulants: avoid or carefully dose other anticoagulant agents.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Orgaran can interact with other medicines that affect haemostasis or drug metabolism.

Major Interactions (Avoid)

  • Concurrent use with other anticoagulants (e.g., unfractionated heparin, warfarin, direct oral anticoagulants) may cause uncontrolled bleeding.
  • Thrombolytic agents (e.g., alteplase) increase risk of severe hemorrhage.
  • Antiplatelet drugs (e.g., clopidogrel, aspirin) when combined can amplify bleeding tendency.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) may modestly increase bleeding risk.
  • Selective serotonin reuptake inhibitors (SSRIs) can affect platelet aggregation.
  • Certain antibiotics (e.g., vancomycin) may alter anticoagulant activity.
  • Herbal supplements such as ginkgo biloba may potentiate anticoagulation.

Frequently Asked Questions

Orgaran is an intravenous anticoagulant indicated for the prevention and treatment of venous thromboembolism, such as deep‑vein thrombosis and pulmonary embolism, and for managing heparin‑induced thrombocytopenia when heparin therapy is contraindicated.

Danaparoid Sodium enhances the activity of antithrombin III and heparin cofactor II, leading to selective inhibition of factor Xa. This reduces thrombin generation and fibrin clot formation while sparing factor IIa, providing anticoagulation with a predictable effect.

The dosing regimen for Orgaran is individualized. The prescribing clinician determines the appropriate dose, infusion rate, and duration based on the patient’s indication, weight, renal function, and laboratory monitoring results.

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 order 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 cold‑chain where required) and import documentation.

Compared with unfractionated heparin, Danaparoid Sodium has a lower risk of inducing heparin‑induced thrombocytopenia and offers more predictable anti‑Xa activity. Unlike low‑molecular‑weight heparins, it is primarily cleared by the reticulo‑endothelial system, making dosing less dependent on renal function.

Orgaran must be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the vial. Keep the product in its original packaging until use to maintain stability and sterility.

Orgaran is given by intravenous infusion. The infusion rate and total dose are set by the prescriber and are typically adjusted according to laboratory monitoring of anti‑Xa activity or activated partial thromboplastin time.

The most serious risks include major bleeding, severe thrombocytopenia, anaphylactic reactions, disseminated intravascular coagulation, and organ hemorrhage such as adrenal or renal bleeding. Prompt recognition and management of these events are essential.

Orgaran is contraindicated in patients with active major bleeding, known hypersensitivity to Danaparoid Sodium or any excipients, and those with a history of severe heparin‑induced thrombocytopenia where alternative anticoagulation is required.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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