Product image of Konakion Mm Paediatric (Phytomenadione) supplied by GNH India

Konakion Mm Paediatric

Active Ingredient:
Phytomenadione
Origin:
EU

Konakion Mm Paediatric (Phytomenadione)

Phytomenadione, the active ingredient in Konakion Mm Paediatric, is a vitamin K presented as an injectable solution for intravenous use. It treats vitamin K deficiency bleeding in newborns and reverses the anticoagulant effects of warfarin in patients who require rapid restoration of clotting.
GNH India supplies Konakion Mm Paediatric as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Neon Healthcare Limited

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Indications & Clinical Uses

Konakion Mm Paediatric provides vitamin K supplementation for conditions affecting the coagulation cascade.

  • Vitamin K deficiency bleeding in newborns: prevents hemorrhage during the first days of life.
  • Warfarin anticoagulation reversal: restores normal clotting in patients receiving warfarin therapy.
  • Prevention of postoperative bleeding in pediatric surgery: ensures adequate coagulation after surgical procedures.

How It Works

  • Phytomenadione acts as a cofactor for the hepatic enzyme gamma‑carboxylase, enabling the gamma‑carboxylation of glutamate residues on clotting factors II, VII, IX and X. This modification is essential for the factors to bind calcium and participate in the coagulation cascade, thereby restoring normal clotting function.

Side Effects

Konakion Mm Paediatric may be associated with several adverse reactions.

Common Side Effects

  • Injection site pain: mild discomfort at the site of administration.
  • Redness or erythema: localized skin irritation.
  • Transient fever: low‑grade temperature rise shortly after injection.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Severe bleeding: paradoxical hemorrhage despite vitamin K administration.
  • Thrombosis or hypotension: abnormal clot formation or sudden drop in blood pressure.

Precautions & Warnings

Use of Konakion Mm Paediatric requires careful clinical consideration.

  • Use only under medical supervision: dosage determined by the prescriber.
  • Check for known hypersensitivity: avoid in patients allergic to phytomenadione or excipients.
  • Monitor coagulation parameters: assess PT/INR after administration.
  • Avoid in severe liver disease: impaired metabolism may affect efficacy.
  • Do not mix with incompatible IV solutions: ensure compatibility before co‑administration.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Phytomenadione can interact with several medications affecting coagulation.

Major Interactions (Avoid)

  • Warfarin: concurrent use may blunt reversal effect.
  • Broad‑spectrum antibiotics (e.g., cephalosporins): may reduce vitamin K synthesis.
  • Other vitamin K preparations: risk of overdose.

Moderate Interactions (Monitor Closely)

  • Heparin: additive anticoagulant effect may increase bleeding risk.
  • Oral contraceptives: potential alteration of clotting balance.
  • Blood products containing vitamin K antagonists: monitor coagulation closely.

Frequently Asked Questions

Konakion Mm Paediatric is used to prevent and treat vitamin K deficiency bleeding in newborns and to reverse the anticoagulant effects of warfarin in patients who need rapid restoration of normal clotting.

Phytomenadione serves as a cofactor for hepatic gamma‑carboxylase, enabling the gamma‑carboxylation of clotting factors II, VII, IX and X. This modification allows the factors to bind calcium and participate effectively in the coagulation cascade.

The dose is determined by the prescribing clinician based on the specific indication, patient weight, age and laboratory values. No fixed regimen is provided here; the prescriber sets the appropriate amount.

Safety data in pregnancy and lactation are limited. It should be used only if clearly needed and prescribed by a qualified health professional after weighing potential benefits and risks.

Submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India works with hospitals, pharmacies and procurement teams, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if required) and import paperwork.

Phytomenadione is the natural vitamin K1 form administered intravenously, offering rapid correction of deficiency. Oral vitamin K preparations are absorbed more slowly and may be less suitable when immediate clotting restoration is required.

Store the product at 2‑8 °C, keep it in the original packaging, protect it from light, and do not freeze or shake. Allow the solution to reach room temperature before use if the label advises.

The medication is administered by intravenous injection or infusion under medical supervision, typically as a single dose or repeated doses as directed by the treating clinician.

Serious adverse reactions include anaphylaxis, severe bleeding, thrombosis and hypotension. If any of these occur, immediate medical attention is required.

Patients with known hypersensitivity to phytomenadione or any component of the formulation, and those with severe liver dysfunction where vitamin K metabolism is compromised, should avoid using this product.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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