Product image of Konakion (Phytomenadione) supplied by GNH India

Konakion

Active Ingredient:
Phytomenadione
Origin:
EU

Konakion (Phytomenadione)

Phytomenadione, the active ingredient in Konakion, is a vitamin K (phytomenadione) presented as an injectable formulation for intramuscular, intravenous and oral use. It is employed to prevent and treat vitamin K deficiency, to protect newborns from hemorrhagic disease, and to reverse the anticoagulant effects of agents such as warfarin.

GNH India supplies Konakion as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Cheplapharm Arzneimittel Gmbh

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Indications & Clinical Uses

Konakion (phytomenadione) acts as a vitamin K replacement to support the coagulation cascade.

  • Vitamin K deficiency: restores normal clotting factor activity in patients with deficient levels.
  • Hemorrhagic disease of the newborn: provides prophylaxis to newborns at risk of bleeding.
  • Anticoagulant therapy reversal: rapidly reverses the effects of warfarin or other vitamin K antagonists.

How It Works

  • Phytomenadione serves as a cofactor for the γ‑carboxylation of glutamate residues on clotting factors II, VII, IX and X in the liver. This post‑translational modification enables calcium binding, essential for assembling the prothrombinase complex and generating thrombin, thereby restoring normal hemostasis.

Side Effects

Adverse reactions to Konakion are generally infrequent but may occur following parenteral or oral administration.

Common Side Effects

  • Injection site pain: mild discomfort at the site of intramuscular or intravenous administration.
  • Nausea: transient feeling of queasiness after oral dosing.
  • Headache: mild headache reported in some patients.
  • Fever: low‑grade temperature elevation occasionally observed.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Hemolysis: rare destruction of red blood cells leading to anemia.
  • Hypercoagulability: uncommon excessive clot formation, especially in patients with underlying thrombophilia.

Precautions & Warnings

When using Konakion, clinicians should observe several safety considerations to minimize risk.

  • Assess vitamin K status: evaluate baseline coagulation parameters before administration.
  • Monitor anticoagulated patients: check INR or PT values after reversal therapy.
  • Use caution in newborns: ensure appropriate dosing and observe for signs of bleeding.
  • Avoid in patients with known hypersensitivity: discontinue if allergic reaction occurs.
  • Pregnancy and lactation: use only if benefit outweighs potential risk, as data are limited.
  • Store at ambient temperature: keep below 25 °C, protect from moisture and light in original packaging.

Avoid Interactions

Konakion may interact with other medicines that affect coagulation or vitamin K metabolism.

Major Interactions (Avoid)

  • Warfarin: concurrent use can blunt anticoagulant effect, requiring dose adjustment.
  • Broad‑spectrum antibiotics (e.g., cephalosporins): may reduce gut flora‑derived vitamin K, altering response.
  • High‑dose vitamin K supplements: can diminish the intended reversal effect.

Moderate Interactions (Monitor Closely)

  • Heparin: combined effect on clotting may increase bleeding risk.
  • Oral contraceptives: potential alteration of coagulation balance.
  • Lipid‑lowering agents (e.g., statins): may affect vitamin K‑dependent pathways.

Frequently Asked Questions

Konakion contains phytomenadione, a form of vitamin K, and is used to prevent or treat vitamin K deficiency, to protect newborns from hemorrhagic disease, and to reverse the anticoagulant effects of drugs such as warfarin.

Phytomenadione acts as a cofactor for the γ‑carboxylation of clotting factors II, VII, IX and X. This modification enables calcium binding, which is essential for the formation of active clotting complexes and the restoration of normal blood coagulation.

The dose of Konakion is determined by the prescribing healthcare professional based on the patient’s clinical condition, age, weight and the specific indication. Only a qualified prescriber should set the appropriate regimen.

Safety data for phytomenadione in pregnancy and lactation are limited. It should be used only when the potential benefit to the mother or infant outweighs any possible risk, and the decision must be made by a qualified healthcare provider.

To order Konakion, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.

Konakion provides phytomenadione, a natural vitamin K1 analogue, which is comparable in efficacy to other vitamin K preparations such as phytonadione. Choice of product often depends on formulation, route of administration, local availability and specific clinical guidelines.

Konakion should be stored at ambient temperature, below 25 °C, in its original packaging. Protect it from moisture and direct light to maintain stability and potency.

Konakion can be given by intramuscular, intravenous or oral routes, depending on the clinical situation and the prescriber's recommendation. The appropriate route and technique are selected by the healthcare professional.

Serious risks include severe allergic reactions such as anaphylaxis, hemolysis leading to anemia, and rare cases of hypercoagulability that may cause unwanted clot formation. Immediate medical attention is required if any of these events occur.

Konakion is contraindicated in individuals with a known hypersensitivity to phytomenadione or any component of the formulation. It should also be used with caution in patients with a history of severe allergic reactions or those at risk for hypercoagulable states.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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