Product image of Kwas Traneksamowy Tillomed (Tranexamic Acid) supplied by GNH India

Kwas Traneksamowy Tillomed

Active Ingredient:
Tranexamic Acid
Origin:
EU

Kwas Traneksamowy Tillomed (Tranexamic Acid)

Tranexamic Acid, the active ingredient in Kwas Traneksamowy Tillomed, is an antifibrinolytic presented as an intravenous solution for intravenous use. It helps control surgical bleeding, trauma‑related hemorrhage, heavy menstrual bleeding, and is used for prophylaxis of hereditary angioedema in appropriate patients.

GNH India supplies Kwas Traneksamowy Tillomed as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Tillomed Pharma Gmbh

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Indications & Clinical Uses

Tranexamic Acid acts on the fibrinolytic pathway to reduce bleeding in several clinical settings.

  • Surgical bleeding control: stabilises clot formation during and after operative procedures.
  • Trauma‑related hemorrhage: limits blood loss in acute injury management.
  • Heavy menstrual bleeding: reduces menstrual blood loss in women with menorrhagia.
  • Hereditary angioedema prophylaxis: helps prevent swelling episodes when used as prescribed.

How It Works

  • Tranexamic Acid competitively inhibits the activation of plasminogen to plasmin by binding to lysine‑binding sites on plasminogen. This reduces fibrinolysis, allowing formed fibrin clots to persist longer and thereby decreasing bleeding. The drug does not affect platelet function and works systemically after intravenous administration.

Side Effects

Tranexamic Acid is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal discomfort.
  • Vomiting: occasional episodes following infusion.
  • Diarrhoea: loose stools reported in some patients.
  • Headache: transient mild headache.
  • Dizziness: occasional light‑headedness.
  • Injection site pain: mild discomfort at the infusion site.

Serious or Rare Side Effects

  • Thromboembolic events: rare clot formation in veins or arteries.
  • Hypotension: sudden drop in blood pressure during infusion.
  • Visual disturbances: rare reports of blurred vision.
  • Allergic reactions: rash, urticaria, or anaphylaxis in susceptible individuals.
  • Renal impairment: worsening kidney function in patients with pre‑existing disease.
  • Seizures: extremely rare neurological events.

Precautions & Warnings

Tranexamic Acid should be used with caution in specific clinical situations.

  • Renal function: assess creatinine clearance before initiating therapy.
  • History of thrombosis: evaluate risk of clot formation prior to use.
  • Concomitant anticoagulants: monitor coagulation parameters closely.
  • Pregnancy and lactation: consider potential risks and benefits; use only if clearly indicated.
  • Pediatric use: dosage and safety must be determined by a qualified prescriber.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Tranexamic Acid may interact with other medicines that affect haemostasis.

Major Interactions (Avoid)

  • Combined hormonal contraceptives: increased risk of thrombosis.
  • Estrogen‑containing hormone therapy: heightened clotting potential.
  • Direct oral anticoagulants (DOACs): may reduce anticoagulant efficacy.

Moderate Interactions (Monitor Closely)

  • Antiplatelet agents (e.g., aspirin, clopidogrel): monitor for bleeding or clotting balance.
  • Fibrinolytic agents (e.g., alteplase): antagonistic effect may diminish therapeutic action.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): increased bleeding risk when used together.

Frequently Asked Questions

Kwas Traneksamowy Tillomed contains tranexamic acid and is used to reduce excessive bleeding in surgical procedures, trauma‑related hemorrhage, heavy menstrual bleeding, and as prophylaxis for hereditary angioedema when prescribed by a qualified healthcare professional.

Tranexamic acid blocks the conversion of plasminogen to plasmin by binding to lysine‑binding sites on plasminogen. This inhibition reduces fibrinolysis, allowing blood clots to remain stable longer and thereby decreasing bleeding.

The dosage of Kwas Traneksamowy Tillomed is determined by the prescribing clinician based on the specific indication, patient weight, renal function, and clinical situation. Only a qualified prescriber should set the appropriate dose.

Safety data for tranexamic acid in pregnancy and lactation are limited. It should only be used when the potential benefit justifies any potential risk to the fetus or infant, and the decision must be made by a healthcare professional.

To place an order, 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 necessary import documentation.

Tranexamic acid, the active ingredient in Kwas Traneksamowy Tillomed, is a synthetic lysine analogue and is generally preferred over older agents like epsilon‑aminocaproic acid due to its higher potency, better tolerability, and more predictable pharmacokinetics when administered intravenously.

Kwas Traneksamowy Tillomed should be stored at 2‑8 °C, kept refrigerated, protected from light, and must not be frozen or shaken. Follow the label instructions and ensure the container remains sealed until use.

The product is supplied as an intravenous solution and is administered by slow infusion into a vein under the supervision of a qualified healthcare professional, following the dosing regimen prescribed for the specific clinical indication.

The most serious risks include rare thromboembolic events such as deep‑vein thrombosis or pulmonary embolism, severe hypotension during rapid infusion, and, in very rare cases, seizures or allergic reactions that may require immediate medical attention.

Patients with a known hypersensitivity to tranexamic acid, active thromboembolic disease, or those who are currently receiving fibrinolytic therapy should not use this product unless specifically directed by a physician after careful risk assessment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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