Product image of Heparin Ratiopharm (Heparin Sodium) supplied by GNH India

Heparin Ratiopharm

Active Ingredient:
Heparin Sodium
Origin:
EU

Heparin Ratiopharm (Heparin Sodium)

Heparin Ratiopharm is a medicinal product that contains the active ingredient heparin sodium. It is supplied in an injectable form for subcutaneous administration, and it is marketed in the European Union. The preparation is classified as an anticoagulant and is used to reduce the risk of blood clot formation in clinical settings. It belongs to the antithrombotic therapeutic class and follows the ATC code B01AB01.

Manufacturer / TM Owner

Ratiopharm Gmbh

1
Pack/s
This product is added to your enquiry list

Request a Quote

Please fill out the form below and our team will get back to you shortly with pricing and further information.

A minimum order value applies. Our team will confirm the exact amount or quantity after reviewing your requirements.

Indications & Clinical Uses

Heparin Ratiopharm is indicated for the prevention and treatment of thromboembolic disorders where anticoagulation is required.

  • Prevention of deep‑vein thrombosis (DVT) following surgery or prolonged immobilisation.
  • Prophylaxis of pulmonary embolism in at‑risk patients.
  • Treatment of acute coronary syndromes, including unstable angina.
  • Management of clotting in patients undergoing haemodialysis or extracorporeal circuits.
  • Adjunct therapy during cardiac surgery to maintain anticoagulation.

Side Effects

The safety profile of Heparin Ratiopharm reflects the typical effects observed with heparin sodium administered subcutaneously.

Common

  • Minor bruising or bleeding at the injection site.
  • Small haematomas or superficial skin erythema.
  • Transient elevation of liver enzymes.
  • Mild nausea or headache.

Serious

  • Heparin‑induced thrombocytopenia (HIT) with a rapid drop in platelet count.
  • Major bleeding events such as gastrointestinal or intracranial haemorrhage.
  • Allergic reactions ranging from urticaria to anaphylaxis.

Precautions & Warnings

When prescribing Heparin Ratiopharm, clinicians should consider several precautionary measures to minimise risk.

  • Assess baseline coagulation parameters and platelet count before initiating therapy.
  • Adjust dose in patients with renal impairment or those receiving concurrent anticoagulants.
  • Monitor for signs of bleeding, especially in the gastrointestinal or central nervous system.
  • Avoid use in individuals with a known history of heparin‑induced thrombocytopenia.
  • Use caution during pregnancy and lactation; evaluate risk‑benefit ratio.
  • Re‑evaluate therapy regularly in elderly patients or those with hepatic dysfunction.

Avoid Interactions

Heparin sodium may interact with a range of medications, influencing its anticoagulant effect.

Avoid

  • Concurrent use of other anticoagulants (e.g., warfarin, direct oral anticoagulants) that markedly increase bleeding risk.
  • Antiplatelet agents such as aspirin, clopidogrel, or non‑steroidal anti‑inflammatory drugs (NSAIDs).
  • Thrombolytic drugs (e.g., alteplase, streptokinase).

Use with caution

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) at low doses, requiring close monitoring of bleeding.
  • Selective serotonin reuptake inhibitors (SSRIs) or other serotonergic agents that may impair platelet function.
  • High‑dose corticosteroids, which can potentiate anticoagulant effects.

Frequently Asked Questions

Heparin Ratiopharm contains heparin sodium as its active pharmaceutical ingredient.

The product is supplied for subcutaneous injection, a common route for anticoagulant therapy.

It is classified as an antithrombotic anticoagulant.

The ATC classification for this medication is B01AB01.

Heparin sodium activates antithrombin III, which then inhibits thrombin (IIa) and factor Xa, reducing clot formation.

Yes, it is commonly used for prophylaxis of deep‑vein thrombosis after surgery or prolonged immobility.

It may be used to manage clotting in patients undergoing haemodialysis or other extracorporeal procedures, under medical supervision.

Typical side effects include minor bruising at the injection site, small haematomas, mild skin redness, transient liver enzyme changes, nausea, or headache.

Serious reactions can include heparin‑induced thrombocytopenia, major bleeding such as gastrointestinal or intracranial haemorrhage, and severe allergic responses.

Yes, patients with a known history of heparin‑induced thrombocytopenia should not receive heparin products.

Concurrent use with warfarin can markedly increase bleeding risk and is generally avoided unless closely monitored.

Use during pregnancy requires a careful risk‑benefit assessment by a healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

Disclaimer

At GNH India, we aim to provide information that is expert-reviewed, accurate, and reliable. However, all content on this platform is intended for general informational purposes only and does not constitute professional medical advice, diagnosis, or treatment. While efforts are made to maintain accuracy and currency, the information may contain errors, omissions, or may not reflect the latest developments. Always consult a qualified healthcare professional regarding any medical concerns.

All product names, brand names, trademarks and registered trademarks displayed on this website are the property of their respective owners. This website and its operator are not affiliated with, endorsed by, or authorized by any such trade mark owners unless expressly stated. Any reference to product names or trademarks is made solely for descriptive and informational purposes. No commercial relationship, sponsorship, approval, or association with any trademark owner should be inferred. Information provided herein does not constitute promotion, advertising, or an offer for sale of any medicinal product and is intended solely for general informational purposes.

All trademarks and brand names displayed on this website are used strictly in accordance with the provisions of the Trade Marks Act, 1999, specifically Sections 30 and 30(1) governing fair use. Trademark ownership has been accurately attributed under the "Manufacturer/ TM Owner" section in compliance with statutory requirements.

Ordering Process

Simple, Secure, and Seamless

Learn how our streamlined ordering process guarantees fast, compliant, and reliable access to essential medicines worldwide.

Quote request form

01

Submit Quote Request Form

Tell us what medications you need by filling out our simple form and uploading a valid document.

Price estimate review

02

We Review & Send Estimate

Our licensed pharmacists will verify your details and provide you with a detailed cost estimate.

Secure payment

03

Confirm & Make Payment

Discuss any queries, approve the estimate, and complete your payment.

Worldwide delivery

04

Get Delivered

Your medicines, safely packed and delivered to your door or nearest airport — hassle-free.

Quality You Can Trust

Our internationally recognized certifications underscore our commitment to safety, quality, and excellence.