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

Konakion Paediatric

Active Ingredient:
Phytomenadione
Origin:
EU

Konakion Paediatric (Phytomenadione)

Phytomenadione, the active ingredient in Konakion Paediatric, is a Vitamin K presented as a sterile solution for intramuscular, intravenous, and oral use. It prevents and treats vitamin K deficiency bleeding in newborns and reverses anticoagulant effects when required, providing rapid restoration of clotting factor activity in pediatric patients.

GNH India supplies Konakion Paediatric as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company follows stringent quality standards and offers reliable efficient logistics for global distribution.

Manufacturer / TM Owner

Cheplapharm Arzneimittel Gmbh

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Indications & Clinical Uses

Konakion Paediatric, a vitamin K preparation, acts on the coagulation cascade to correct deficiencies.

  • Vitamin K deficiency bleeding in newborns: prevents hemorrhagic disease by supplying essential cofactor for clotting factor activation.
  • Vitamin K deficiency bleeding in infants and children: treats active bleeding episodes and restores normal clotting.
  • Anticoagulant reversal: counteracts the effects of vitamin K antagonists such as warfarin in pediatric patients when rapid normalization of coagulation is needed.

How It Works

  • Phytomenadione functions as a cofactor for the γ‑carboxylation of glutamic acid residues on clotting factors II, VII, IX and X in the liver. This enzymatic modification enables the factors to bind calcium, a critical step for their activation in the coagulation cascade, thereby restoring normal clotting ability. The process occurs in the presence of reduced vitamin K, which is regenerated by the enzyme vitamin K epoxide reductase, completing the cycle.

Side Effects

Phytomenadione may be associated with several adverse reactions, ranging from mild to severe.

Common Side Effects

  • Injection site pain
  • Redness or swelling at the administration site
  • Mild fever
  • Transient flushing

Serious or Rare Side Effects

  • Anaphylactic reaction
  • Severe hypersensitivity including rash and angioedema
  • Hemolysis
  • Thrombosis (rare)

Precautions & Warnings

When using Konakion Paediatric, several precautions should be observed to ensure safety.

  • Assess vitamin K status: verify deficiency before administration.
  • Hypersensitivity: avoid in patients with known allergy to phytomenadione or excipients.
  • Anticoagulant therapy: monitor coagulation parameters if used alongside warfarin.
  • Neonatal use: follow recommended prophylaxis schedule for newborns.
  • Concomitant medications: consider potential interactions with drugs affecting vitamin K metabolism.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Warfarin: may diminish anticoagulant effect, requiring dose adjustment.
  • Broad‑spectrum antibiotics (e.g., cephalosporins): can reduce intestinal vitamin K synthesis, affecting response.
  • Bile acid sequestrants: may decrease absorption of oral phytomenadione.

Moderate Interactions (Monitor Closely)

  • Heparin: additive anticoagulant effect may increase bleeding risk.
  • Oral contraceptives: may enhance clotting factor activity, requiring monitoring.
  • Phenobarbital or other enzyme inducers: may increase metabolism of vitamin K, reducing efficacy.

Frequently Asked Questions

Konakion Paediatric is used to prevent and treat vitamin K deficiency bleeding in newborns and infants, and to reverse the anticoagulant effects of vitamin K antagonists such as warfarin when rapid correction of clotting is required.

Phytomenadione acts as a cofactor for the γ‑carboxylation of clotting factors II, VII, IX and X, enabling these proteins to bind calcium and become fully active in the coagulation cascade, which restores normal blood clotting function.

The dose of Konakion Paediatric is determined by the prescribing clinician based on the patient’s age, weight, clinical condition and the route of administration. Exact dosing information should be obtained from the healthcare professional.

Safety data for phytomenadione in pregnancy and lactation are limited. Use during pregnancy or while breastfeeding should only be considered if clearly indicated by a qualified healthcare provider after weighing potential benefits against possible risks.

To order, 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 (including cold‑chain if needed) and import documentation.

Konakion Paediatric contains phytomenadione, a synthetic form of vitamin K1, and is available for multiple routes (IM, IV, oral). Compared with other vitamin K preparations, it offers flexibility in administration and is formulated specifically for pediatric use, but clinical choice depends on local guidelines and individual patient needs.

Konakion Paediatric should be stored at ambient temperature, protected from moisture and light, and kept in its original container. Do not freeze the product. Follow any additional handling instructions provided on the label to maintain stability.

The product can be given by intramuscular injection, intravenous infusion, or oral administration, depending on the clinical situation and the formulation supplied. Administration technique and site selection should follow standard medical practice and the prescribing information.

Serious risks include rare anaphylactic reactions, severe hypersensitivity, hemolysis, and, very rarely, thrombosis. Prompt recognition of these events and immediate medical intervention are essential. Patients should be monitored for any signs of allergic reaction after administration.

Konakion Paediatric should not be used in individuals with a known hypersensitivity to phytomenadione or any of the product’s excipients. Caution is also advised for patients receiving concurrent anticoagulant therapy or those with disorders affecting vitamin K metabolism, pending medical assessment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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