GNH USA

Europe — EMA

Konakion Mm Paediatric

GNH USA supplies Konakion Mm Paediatric (Phytomenadione), a Vitamin K for vitamin K deficiency, newborn hemorrhage prevention, and anticoagulant reversal.

Phytomenadione

Request sourcing

1
Pack/s

What is Phytomenadione?

Phytomenadione, the active ingredient in Konakion Mm Paediatric, is a Vitamin K presented as a paediatric formulation for intramuscular, intravenous, and oral use. It treats vitamin K deficiency, helps prevent hemorrhage in newborns, and reverses anticoagulant therapy in children. GNH USA supplies Konakion Mm Paediatric as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

What is Phytomenadione used for?

Konakion Mm Paediatric, a Vitamin K analogue, is used in conditions related to impaired coagulation.

- Vitamin K deficiency: restores normal clotting factor activity in deficient patients. - Prevention of hemorrhage in newborns: provides prophylactic vitamin K to reduce risk of neonatal bleeding. - Reversal of anticoagulant therapy: supplies vitamin K to counteract the effects of warfarin and other vitamin K antagonists.

What are the side effects of Phytomenadione?

Adverse reactions may occur with any route of administration.

Common Side Effects: - Injection site pain or erythema. - Mild fever or chills. - Nausea or vomiting. - Diarrhea. - Transient headache. - Local swelling.

Serious or Rare Side Effects: - Anaphylactic reaction or severe hypersensitivity. - Hemolysis or severe anemia. - Thrombosis or paradoxical clot formation. - Severe bleeding despite therapy. - Elevated liver enzymes. - Acute renal impairment.

What precautions apply to Phytomenadione?

Use with clinical judgment and monitor patients closely.

- Assess vitamin K status before initiating therapy. - Monitor coagulation parameters (PT/INR) during treatment. - Use with caution in patients with hepatic impairment. - Avoid in individuals with known hypersensitivity to phytomenadione. - Follow neonatal dosing guidelines when used for newborn prophylaxis. - Store at ambient temperature: keep in the original container, protect from moisture and light.

What does Phytomenadione interact with?

Phytomenadione may alter the effect of several drugs.

Major Interactions (Avoid): - Coumarin anticoagulants (e.g., warfarin): may reduce anticoagulant effect. - Broad‑spectrum antibiotics that disrupt gut flora: can increase vitamin K deficiency risk. - Cholestyramine or other bile‑acid sequestrants: may decrease absorption of vitamin K.

Moderate Interactions (Monitor Closely): - Rifampin: may increase hepatic metabolism of vitamin K. - Phenobarbital: may enhance vitamin K clearance. - Cephalosporins: may interfere with vitamin K synthesis. - Direct oral anticoagulants: monitor coagulation status if combined.

Frequently asked questions

What is Konakion Mm Paediatric used for?+
Konakion Mm Paediatric is used to treat vitamin K deficiency, to prevent bleeding in newborns, and to reverse the effects of anticoagulant therapy such as warfarin in pediatric patients. It provides the essential cofactor needed for normal clotting factor activation.
How does phytomenadione work in the body?+
Phytomenadione serves as a cofactor for the enzyme gamma‑glutamyl carboxylase, which adds a carboxyl group to specific glutamate residues on clotting factors II, VII, IX, and X. This modification enables the factors to bind calcium and become biologically active, restoring normal blood coagulation.
What is the usual dose of Konakion Mm Paediatric?+
The dose of Konakion Mm Paediatric is determined by the prescribing clinician based on the patient’s age, weight, clinical condition, and route of administration. Healthcare professionals follow established guidelines and adjust the amount as needed for each individual case.
Is Konakion Mm Paediatric safe to use during pregnancy or breastfeeding?+
Safety data for phytomenadione in pregnancy and lactation are limited. The product should only be used if the potential benefit justifies any potential risk to the fetus or infant, and this decision must be made by a qualified healthcare provider.
How do I order Konakion Mm Paediatric from GNH USA?+
To order, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA works with 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.
How does Konakion Mm Paediatric compare with other vitamin K products?+
Konakion Mm Paediatric contains phytomenadione, the same active form of vitamin K1 found in most vitamin K preparations. Compared with synthetic analogues, phytomenadione has a well‑established safety profile and is widely used for neonatal prophylaxis and anticoagulant reversal, offering reliable bioavailability across multiple routes.
What are the storage and handling requirements for Konakion Mm Paediatric?+
Store the product at ambient temperature, preferably below 25 °C. Keep it in the original packaging, protect it from moisture and direct light, and avoid exposure to extreme temperatures. Follow any additional handling instructions provided by the manufacturer.
How is Konakion Mm Paediatric administered?+
Konakion Mm Paediatric can be given by intramuscular injection, intravenous infusion, or oral administration, depending on the clinical situation and the prescriber's judgment. The route is selected to achieve the desired therapeutic effect while considering patient age and condition.
What are the most serious risks associated with Konakion Mm Paediatric?+
Serious risks include severe allergic reactions such as anaphylaxis, hemolysis, thrombosis, and paradoxical bleeding despite therapy. Patients should be monitored for signs of hypersensitivity, sudden drop in blood pressure, or unexpected bleeding, and medical attention should be sought immediately if these occur.
Who should not use Konakion Mm Paediatric?+
Konakion Mm Paediatric should be avoided in individuals with a known hypersensitivity to phytomenadione or any of the product’s excipients. It should also be used with caution in patients with severe liver disease or those receiving medications that may interact significantly, as directed by a healthcare professional.
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
Neon Healthcare Limited
Origin
EU

Related products