Product image of Konakion Novum (Phytomenadione) supplied by GNH India

Konakion Novum

Active Ingredient:
Phytomenadione
Origin:
EU

Konakion Novum (Phytomenadione)

Phytomenadione, the active ingredient in Konakion Novum, is a vitamin K hemostatic agent presented as an injectable preparation for intramuscular, intravenous, and oral use. It restores normal coagulation in patients with vitamin K deficiency, counteracts bleeding associated with anticoagulant therapy, and provides neonatal prophylaxis against hemorrhagic disease.

GNH India supplies Konakion Novum as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide, ensuring quality and regulatory compliance across all markets through rigorous manufacturing standards and validated distribution processes.

Manufacturer / TM Owner

Cheplapharm Arzneimittel Gmbh

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Indications & Clinical Uses

Konakion Novum, a vitamin K hemostatic agent, is used to manage disorders of coagulation related to vitamin K deficiency.

  • Vitamin K deficiency: restores clotting factor activity to correct bleeding tendencies.
  • Anticoagulant‑associated bleeding: reverses the effects of warfarin and other vitamin K antagonists to stop hemorrhage.
  • Neonatal hemorrhagic disease prophylaxis: prevents bleeding in newborns at risk of vitamin K deficiency.
  • Pre‑operative preparation: ensures adequate clotting status before surgical procedures in patients with low vitamin K levels.

How It Works

  • Phytomenadione acts as a co‑factor for the enzyme γ‑glutamyl carboxylase, enabling γ‑carboxylation of glutamic acid residues on clotting factors II, VII, IX and X. This post‑translational modification generates functional calcium‑binding sites, allowing the factors to participate in the coagulation cascade and thereby restoring normal hemostasis. The restored activity of these vitamin K‑dependent proteins accelerates the conversion of prothrombin to thrombin and supports fibrin formation, essential steps in clot development.

Side Effects

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

Common Side Effects

  • Injection site pain: mild discomfort or tenderness at the site of administration.
  • Erythema: redness of the skin around the injection area.
  • Nausea: transient feeling of queasiness.
  • Headache: mild to moderate headache.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction with difficulty breathing, swelling, and hypotension.
  • Hemolysis: destruction of red blood cells leading to anemia.
  • Thrombosis: formation of abnormal clots in blood vessels.
  • Elevated liver enzymes: signs of hepatic stress or injury.

Precautions & Warnings

When using Konakion Novum, several precautions should be observed to ensure safe administration.

  • Allergy assessment: verify no known hypersensitivity to phytomenadione or excipients.
  • Bleeding disorders: monitor coagulation parameters in patients with existing clotting abnormalities.
  • Concurrent anticoagulants: adjust dosing and observe for over‑correction of anticoagulation.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk, as safety data are limited.
  • Neonatal use: follow established dosing guidelines and monitor bilirubin levels.
  • Store at ambient temperature: keep below 25 °C, protect from moisture and light, retain in original packaging.

Avoid Interactions

Phytomenadione can interact with several medicines, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Warfarin and other vitamin K antagonists: concurrent use may diminish anticoagulant effect, requiring close monitoring.
  • Broad‑spectrum antibiotics (e.g., cephalosporins): may reduce vitamin K synthesis, increasing need for phytomenadione.
  • High‑dose vitamin K supplements: may counteract therapeutic action.

Moderate Interactions (Monitor Closely)

  • Heparin: combined anticoagulant therapy may increase bleeding risk.
  • Oral contraceptives: may alter vitamin K metabolism, necessitating observation.
  • Lipid‑lowering agents (statins): potential effect on vitamin K‑dependent pathways.

Frequently Asked Questions

Konakion Novum contains phytomenadione, a vitamin K analogue used to treat vitamin K deficiency, reverse bleeding caused by anticoagulant therapy such as warfarin, and provide prophylaxis against hemorrhagic disease in newborns. It is employed in clinical settings where rapid restoration of clotting factor activity is required.

Phytomenadione serves as a co‑factor for the γ‑glutamyl carboxylase enzyme, enabling the γ‑carboxylation of clotting factors II, VII, IX and X. This modification creates calcium‑binding sites essential for the activation of these factors, thereby re‑establishing the normal coagulation cascade and stopping bleeding.

The dose of Konakion Novum is individualized and set by the prescribing healthcare professional based on the patient’s age, clinical condition, severity of deficiency, and route of administration. No fixed regimen is provided here; clinicians calculate the appropriate amount according to current medical guidelines.

Safety data for phytomenadione in pregnancy and lactation are limited. It may be used only when the potential benefit to the mother or infant outweighs any possible risk. The decision should be made by a qualified clinician after evaluating the specific clinical scenario.

To request Konakion Novum, 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 if needed) and necessary import documentation.

Konakion Novum provides phytomenadione in injectable form, allowing rapid systemic absorption, whereas oral vitamin K tablets (phytonadione) have slower onset and may be less suitable for emergency reversal of anticoagulation. The injectable route is preferred for neonates and patients unable to take oral medication, offering more predictable plasma levels.

Konakion Novum should be stored at ambient temperature, preferably below 25 °C, protected from moisture and direct light. Keep the product in its original packaging until use and avoid freezing. Inspect the vial for particulate matter before administration and discard if any abnormalities are observed.

The drug can be given by intramuscular, intravenous, or oral routes, depending on the clinical indication and patient condition. Intravenous injection provides the fastest effect for acute bleeding, while intramuscular administration is common for neonatal prophylaxis. Oral formulations are used for maintenance therapy in chronic deficiency.

Serious adverse reactions include anaphylaxis, hemolysis, thrombosis, and significant elevations in liver enzymes indicating hepatic injury. Patients should be monitored closely for signs of allergic response, unexpected clot formation, or liver dysfunction, and immediate medical attention should be sought if such events occur.

Konakion Novum is contraindicated in individuals with known hypersensitivity to phytomenadione or any of its excipients. Caution is also advised for patients with severe liver disease, uncontrolled bleeding disorders, or those receiving high‑dose vitamin K supplements without medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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