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 presented as an injectable solution for intramuscular, intravenous, or oral use. It treats vitamin K deficiency, helps prevent hemorrhage in newborns, and reverses anticoagulation caused by warfarin or other vitamin K antagonists.

GNH India supplies Konakion Novum as a licensed, GDP‑compliant international pharmaceutical supplier, providing the product to hospitals, pharmacies, transplant centres and clinics worldwide with reliable logistics and quality assurance. Our network ensures timely delivery and compliance with local regulatory requirements.

Manufacturer / TM Owner

Cheplapharm Arzneimittel Gmbh

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Indications & Clinical Uses

Konakion Novum (phytomenadione) is used to correct disorders of the vitamin K‑dependent clotting cascade.

  • Vitamin K deficiency: restores normal clotting factor activity and reduces bleeding risk.
  • Newborn hemorrhage prevention: provides essential vitamin K to newborns to lower incidence of early‑life bleeding.
  • Warfarin reversal: rapidly re‑establishes coagulation in patients over‑anticoagulated with vitamin K antagonists.

How It Works

  • Phytomenadione serves as a cofactor for the enzyme γ‑glutamyl carboxylase, enabling γ‑carboxylation of glutamate residues on clotting factors II, VII, IX and X. This post‑translational modification allows the factors to bind calcium ions and participate effectively in the coagulation cascade, thereby restoring normal hemostasis in individuals with vitamin K deficiency or antagonism.

Side Effects

Phytomenadione may cause adverse reactions, ranging from mild to severe.

Common Side Effects

  • Injection site pain: discomfort at the site of intramuscular or intravenous administration.
  • Erythema: localized redness around the injection area.
  • Mild fever: transient elevation of body temperature.
  • Nausea: occasional feeling of queasiness after dosing.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Severe hypersensitivity: including rash, swelling, or respiratory distress.
  • Thrombosis: formation of abnormal blood clots.
  • Hemolysis: destruction of red blood cells.
  • Elevated liver enzymes: indicating hepatic stress.
  • Disseminated intravascular coagulation: widespread clotting abnormalities.

Precautions & Warnings

Before using Konakion Novum, consider the following safety measures.

  • Assess vitamin K status before use: evaluate baseline coagulation parameters.
  • Monitor coagulation parameters after administration: check INR or PT as appropriate.
  • Use with caution in patients with liver disease: hepatic impairment may affect metabolism.
  • Avoid in individuals with known hypersensitivity to phytonadione: discontinue if allergic signs appear.
  • Pregnancy and lactation: administer only if the expected benefit justifies the potential risk.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Konakion Novum can interact with several medicines; awareness helps prevent reduced efficacy or increased risk.

Major Interactions (Avoid)

  • Warfarin: antagonizes anticoagulant effect, reducing therapeutic benefit.
  • Broad‑spectrum antibiotics (e.g., cephalosporins): may alter gut flora and affect vitamin K levels.
  • Other vitamin K antagonists (e.g., acenocoumarol): reduced efficacy when co‑administered.

Moderate Interactions (Monitor Closely)

  • Cefoperazone and cefamandole: may increase bleeding risk when combined.
  • Barbiturates: may increase vitamin K metabolism, potentially requiring dose adjustment.
  • Oral contraceptives: may affect clotting parameters and warrant monitoring.

Frequently Asked Questions

Konakion Novum contains phytomenadione, a form of vitamin K, and is used to correct vitamin K deficiency, prevent bleeding in newborns, and reverse the anticoagulant effects of warfarin or other vitamin K antagonists. These indications address disorders of the clotting cascade where normal coagulation is impaired.

Phytomenadione acts as a cofactor for the enzyme γ‑glutamyl carboxylase, enabling the γ‑carboxylation of specific glutamate residues on clotting factors II, VII, IX and X. This chemical modification allows the factors to bind calcium and function properly in the coagulation cascade, thereby restoring normal blood clotting.

The dose of Konakion Novum is individualized and set by the prescribing healthcare professional based on the patient’s clinical condition, age, weight, and the severity of vitamin K deficiency or anticoagulation. Dosage regimens are not standardized and should follow the prescriber’s instructions.

The pregnancy category for phytomenadione is not definitively established. It should be used in pregnancy or while breastfeeding only when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and under the guidance of a qualified healthcare provider.

To order 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 where required) and necessary import documentation.

Konakion Novum is a phytomenadione formulation comparable to other injectable vitamin K1 products. Its clinical efficacy in correcting deficiency and reversing anticoagulation is similar, but formulation differences (e.g., excipients, stability) may affect storage requirements and handling. Selection often depends on supplier reliability, regulatory status, and specific institutional protocols.

Konakion Novum should be stored at 2‑8 °C, protected from light, and kept in its original container. It must not be frozen or shaken vigorously. If temperature excursions occur, the product should be inspected for discoloration or precipitation before use.

Konakion Novum can be given by intramuscular, intravenous, or oral routes, depending on the clinical situation and prescriber’s judgment. Injection techniques follow standard aseptic practices, and oral administration uses the appropriate liquid or tablet formulation if available.

The most serious adverse reactions include anaphylaxis, severe hypersensitivity, thrombosis, hemolysis, and disseminated intravascular coagulation. Prompt recognition of these events and immediate medical intervention are essential to mitigate potential harm.

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 concurrent high‑dose vitamin K antagonists without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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