GNH USA

Europe — EMA

Konakion Mm Paediatric Ampoules

GNH USA supplies Konakion Mm Paediatric Ampoules (Phytomenadione), a vitamin K for prevention of hemorrhagic disease of the newborn and reversal of warfarin

Phytomenadione

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What is Phytomenadione?

Phytomenadione, the active ingredient in Konakion Mm Paediatric Ampoules, is a vitamin K presented as an injectable solution for intramuscular, intravenous or oral use. It is employed to prevent and treat vitamin K deficiency bleeding, particularly in newborns, and to reverse anticoagulation caused by warfarin. GNH USA supplies Konakion Mm Paediatric Ampoules as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

What is Phytomenadione used for?

Konakion Mm Paediatric Ampoules provides vitamin K to address disorders of coagulation. - Hemorrhagic disease of the newborn: prevents bleeding in neonates at risk of vitamin K deficiency. - Vitamin K deficiency bleeding: treats active bleeding in infants and children with low vitamin K levels. - Warfarin reversal: restores clotting factor activity in patients requiring rapid anticoagulation reversal. - Surgical prophylaxis: reduces peri‑operative bleeding in patients with impaired vitamin K status.

What are the side effects of Phytomenadione?

Adverse reactions may occur following administration of vitamin K injectable solutions.

Common Side Effects: - Injection site pain or erythema - Mild nausea - Transient headache - Low‑grade fever - Diarrhoea - Dizziness

Serious or Rare Side Effects: - Anaphylactic reaction - Severe hypotension - Hemolysis - Jaundice - Thrombocytopenia - Persistent vomiting

What precautions apply to Phytomenadione?

When using Konakion Mm Paediatric Ampoules, consider the following precautions. - Contraindication: Do not use in patients with known hypersensitivity to phytomenadione or formulation excipients. - Caution in newborns: Monitor for signs of hyperbilirubinemia after administration. - Interaction with anticoagulants: Adjust dosing of concurrent warfarin therapy as needed. - Use in pregnancy: Evaluate risk‑benefit ratio; limited data available. - Storage: Store at 2‑8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Phytomenadione interact with?

Phytomenadione may interact with other medicines affecting coagulation.

Major Interactions (Avoid): - Warfarin: can diminish anticoagulant effect, leading to loss of therapeutic control. - Broad‑spectrum antibiotics (e.g., cephalosporins): may interfere with vitamin K synthesis, requiring careful monitoring.

Moderate Interactions (Monitor Closely): - Rifampin: may increase vitamin K metabolism, reducing efficacy. - Phenobarbital: induces hepatic enzymes that accelerate vitamin K clearance. - Oral contraceptives: potential additive effect on clotting factors, warranting observation.

Frequently asked questions

What is Konakion Mm Paediatric Ampoules used for?+
Konakion Mm Paediatric Ampoules contains phytomenadione, a form of vitamin K, and is used to prevent and treat vitamin K deficiency bleeding in newborns, to reverse the anticoagulant effects of warfarin, and to provide prophylaxis against bleeding in surgical or other clinical situations where clotting support is required.
How does phytomenadione work in the body?+
Phytomenadione serves as a cofactor for the gamma‑carboxylation of specific glutamic acid residues on clotting factors II, VII, IX and X. This biochemical step is essential for producing functional clotting proteins in the liver, thereby restoring normal coagulation and preventing hemorrhage.
What is the usual dose of Konakion Mm Paediatric Ampoules?+
The exact dose of Konakion Mm Paediatric Ampoules is determined by the prescribing clinician based on the patient’s age, weight, clinical condition, and route of administration. Healthcare professionals should follow local guidelines and individual patient needs when prescribing.
Is Konakion Mm Paediatric Ampoules safe to use during pregnancy or breastfeeding?+
Safety data for phytomenadione during pregnancy and lactation are limited. The drug should only be used when the potential benefit to the mother or infant outweighs any possible risk. Clinicians should assess each case individually and discuss any concerns with the patient.
How do I order Konakion Mm Paediatric Ampoules from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams worldwide. After submission, the sales team will verify trade or institutional credentials, then provide pricing, availability, shipping details (including cold‑chain handling if needed) and any required import documentation.
How does Konakion Mm compare with other vitamin K products?+
Konakion Mm Paediatric Ampoules provides phytomenadione in a sterile injectable form, which offers rapid bioavailability compared with oral vitamin K preparations. This can be advantageous in emergency reversal of anticoagulation or in newborn prophylaxis where immediate effect is desired. Other vitamin K products may be oral or have different excipients, influencing stability and administration routes.
What are the storage and handling requirements for Konakion Mm Paediatric Ampoules?+
The ampoules should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep them in the original packaging until use to maintain sterility and potency. If temperature excursions occur, discard the product according to local regulations.
How is Konakion Mm Paediatric Ampoules administered?+
Konakion Mm Paediatric Ampoules can be given by intramuscular, intravenous, or oral routes, depending on the clinical indication and patient condition. Administration should be performed by qualified healthcare personnel following aseptic technique and appropriate dosing guidelines.
What are the most serious risks associated with Konakion Mm Paediatric Ampoules?+
Serious adverse reactions, though rare, include anaphylaxis, severe hypotension, hemolysis, and thrombocytopenia. Immediate medical attention is required if any signs of a severe allergic reaction or unexpected bleeding abnormalities occur after administration.
Who should not use Konakion Mm Paediatric Ampoules?+
Patients with a known hypersensitivity to phytomenadione or any component of the formulation should avoid using the product. Additionally, it should be used with caution in individuals with a history of severe allergic reactions, and it is contraindicated in newborns with certain metabolic disorders unless specifically advised by a specialist.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Phytomenadione
Route
Intramuscular Use , Intravenous Use , Oral Use
Manufacturer
Cheplapharm Arzneimittel Gmbh
Origin
EU

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