GNH USA

Europe — EMA

Neoparin (Enoxaparin Sodium)

GNH USA supplies Neoparin (Enoxaparin Sodium), a low molecular weight heparin for prevention of deep vein thrombosis and pulmonary embolism.

Request sourcing

1
Pack/s

What is Enoxaparin Sodium?

Enoxaparin Sodium, the active ingredient in Neoparin, is a low molecular weight heparin presented as a sterile solution for subcutaneous and intravenous use. It is used to prevent and treat venous thromboembolism in adult patients at risk of clot formation.

GNH USA supplies Neoparin as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

What is Enoxaparin Sodium used for?

Neoparin (enoxaparin sodium) is employed in the management of thromboembolic disorders and related procedural anticoagulation. - Deep vein thrombosis prophylaxis: reduces the incidence of DVT in surgical and medically immobilized patients. - Deep vein thrombosis treatment: facilitates clot resolution and prevents extension in acute DVT. - Pulmonary embolism prevention and treatment: provides anticoagulation to avert or manage PE events. - Anticoagulation during hemodialysis or extracorporeal procedures: maintains circuit patency by inhibiting clot formation.

What are the side effects of Enoxaparin Sodium?

Neoparin may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects: - Injection site erythema or bruising - Minor bleeding (e.g., gum, nosebleeds) - Nausea - Elevated liver enzymes

Serious or Rare Side Effects: - Major hemorrhage (intracranial, gastrointestinal) - Heparin‑induced thrombocytopenia (HIT) - Allergic reactions including anaphylaxis - Spinal or epidural hematoma (with neuraxial procedures)

What precautions apply to Enoxaparin Sodium?

When using Neoparin, clinicians should observe several safety considerations to minimize risk. - Renal function: adjust dose or avoid in severe renal impairment (creatinine clearance <30 mL/min). - Bleeding risk: evaluate for active bleeding, recent surgery, or coagulopathy before initiation. - Concomitant anticoagulants: avoid simultaneous use with other anticoagulants unless specifically indicated. - Pregnancy and lactation: use only if the potential benefit outweighs the potential risk, as safety data are limited. - Monitoring: assess platelet counts periodically to detect heparin‑induced thrombocytopenia. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

What does Enoxaparin Sodium interact with?

Neoparin can interact with other medicines, altering its anticoagulant effect or increasing bleeding risk.

Major Interactions (Avoid): - Concurrent use with other anticoagulants (e.g., warfarin, direct thrombin inhibitors) – may cause uncontrolled bleeding. - Neuraxial anesthesia or spinal puncture – heightened risk of spinal hematoma. - Known heparin‑induced thrombocytopenia – contraindicated due to cross‑reactivity.

Moderate Interactions (Monitor Closely): - Non‑steroidal anti‑inflammatory drugs (NSAIDs) or antiplatelet agents – increase bleeding tendency. - Selective serotonin reuptake inhibitors (SSRIs) or other serotonergic drugs – may potentiate hemorrhagic risk. - ACE inhibitors or angiotensin receptor blockers – may enhance anticoagulant effect in some patients. - Renal‑clearing drugs (e.g., aminoglycosides) – may require dose adjustment of enoxaparin.

Frequently asked questions

What is Neoparin used for?+
Neoparin contains enoxaparin sodium, a low molecular weight heparin that is used to prevent and treat venous thromboembolism. It is indicated for deep‑vein thrombosis prophylaxis, treatment of acute DVT, prevention and management of pulmonary embolism, and anticoagulation during hemodialysis or other extracorporeal procedures.
How does enoxaparin sodium work?+
Enoxaparin sodium binds to antithrombin III, greatly increasing its ability to inhibit activated factor Xa and, to a lesser extent, thrombin (factor IIa). By blocking factor Xa, the cascade that converts prothrombin to thrombin is interrupted, reducing fibrin clot formation while preserving a predictable anticoagulant profile.
What is the usual dose of Neoparin?+
The dose of Neoparin is individualized and set by the prescribing clinician based on the specific indication, patient weight, renal function, and risk factors. Dosing regimens differ for prophylaxis versus treatment and for subcutaneous versus intravenous administration, so the exact amount must be determined by a qualified health professional.
Is Neoparin safe during pregnancy or breastfeeding?+
Safety data for enoxaparin in pregnancy and lactation are limited, and the product is classified as pregnancy category unknown. It may be used during pregnancy only when the potential maternal benefit justifies any possible risk to the fetus, and breastfeeding decisions should be made after consulting a healthcare provider.
How do I order Neoparin from GNH USA?+
To order Neoparin, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies, and procurement teams worldwide, and will request verification of trade or institutional credentials. After confirmation, the team provides pricing, availability, shipping details (including cold‑chain if needed), and assists with import documentation.
How does Neoparin compare with unfractionated heparin?+
Neoparin (enoxaparin) is a low molecular weight heparin, offering more predictable pharmacokinetics, a longer half‑life, and once‑ or twice‑daily dosing compared with unfractionated heparin, which requires continuous infusion and frequent monitoring. Enoxaparin provides greater anti‑Xa activity, lower risk of heparin‑induced thrombocytopenia, and does not usually need routine laboratory monitoring.
How should Neoparin be stored and handled?+
Neoparin should be stored at 2‑8 °C (refrigerated), protected from light, and must not be frozen or shaken vigorously. If temporary storage at controlled room temperature is necessary, keep the product in its original packaging and use it within the time frame specified by the manufacturer.
How is Neoparin administered?+
Neoparin is supplied as a sterile solution for subcutaneous injection or intravenous infusion. The route, injection site, and infusion rate are determined by the prescribing clinician based on the therapeutic indication and patient characteristics. Proper aseptic technique and correct needle length for subcutaneous administration are essential.
What are the most serious risks to watch for with Neoparin?+
The most serious risks include major bleeding events such as intracranial or gastrointestinal hemorrhage, and heparin‑induced thrombocytopenia (HIT), which can paradoxically cause clot formation. Patients should be monitored for signs of unexpected bleeding, sudden drops in platelet count, or allergic reactions, and therapy should be stopped if these occur.
Who should not use Neoparin?+
Neoparin is contraindicated in patients with active major bleeding, a known hypersensitivity to enoxaparin or other LMWHs, and those with a history of heparin‑induced thrombocytopenitis. Caution is also advised in individuals with severe renal impairment (creatinine clearance <30 mL/min) and in patients undergoing neuraxial anesthesia unless specific precautions are taken.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Enoxaparin Sodium
Route
Extracorporeal Use , Intravenous Use , Subcutaneou
Manufacturer
Sciencepharma Spółka Z Ograniczoną Odpowiedzialnością
Origin
EU

Related products