Phytonadione (K1; Phylloquinone; Methylphytyl Naphthoquinone)

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Phytonadione (K1; Phylloquinone; Methylphytyl Naphthoquinone)

  Action
  Indications
  Contraindications
  Route/Dosage
  Interactions
  Lab Test Interferences
  Adverse Reactions
  Precautions
Patient Care Considerations
  Administration/Storage
  Assessment/Interventions
  Patient/Family Education


(fye-toe-nuh-DIE-ohn)
AquaMEPHYTON, Mephyton
Class: Blood modifier/Vitamin K

 Action Promotes hepatic synthesis of active prothrombin (factor II), proconvertin (factor VII), plasma thromboplastin component (factor IX) and Stuart factor (factor X).

 Indications Management of coagulation disorders due to faulty formation of factors II, VII, IX and X when due to vitamin K deficiency or interference with vitamin K activity.

Oral/Parenteral: Treatment of anticoagulant-induced prothrombin deficiency; treatment of hypoprothrombinemia secondary to salicylates or antibacterial therapy or secondary to obstructive jaundice and biliary fistulas, provided bile salts are also given. Parenteral: Treatment of hypoprothrombinemia secondary to conditions limiting absorption or synthesis of vitamin K prophylaxis and therapy of hemorrhagic disease of the newborn.

 Contraindications Standard considerations.

 Route/Dosage

ADULTS & CHILDREN: PO/SC/IM 2.5 to 10 mg (in adults, up to 25 mg for serious bleeding; rarely, 50 mg), may repeat oral dose based on response in 6 to 8 hr or 12 to 48 hr; avoid oral route when disorder would prevent adequate absorption.

Hemorrhagic Disease (Prophylaxis)

NEONATES IM Single dose 0.5 to 1 mg within 1 hr of birth. INFANTS: PO/SC/IM 2 mg.

Hemorrhagic Disease (Treatment)

NEONATES SC/IM 1 mg accompanied by laboratory evaluation.

 Interactions

Oral anticoagulants: Effects are antagonized by vitamin K, particularly in patients with advanced liver disease.

 Lab Test Interferences Paradoxical prolongation of prothrombin time (PT) after maximum doses of vitamin K.

 Adverse Reactions

CV: Hypotension; cyanosis. CNS: Headache; dizziness. DERM: Pruritic erythematous plaques at IM injection site; rash; urticaria. HEPA: Hyperbilirubinemia, including kernicterus, in newborns. OTHER: Anaphylactoid reactions; pain, swelling and tenderness at injection site; death after IV injection.

 Precautions

Pregnancy: Category C. Lactation: Vitamin K excreted in breast milk. Anticoagulation: Patient may be refractory to oral anticoagulants, particularly large doses. Bleeding: Giving vitamin K has no immediate coagulant effect. Management of bleeding involves standard measures (eg, transfusions). Hypersensitivity: Rash and urticaria; anaphylactoid reactions. Impaired hepatic function: Giving vitamin K to correct hypoprothrombinemia associated with severe hepatitis or cirrhosis may further depress prothrombin concentration. IV administration: Deaths have occurred; restrict this route to situations in which other routes of administration are not feasible.


PATIENT CARE CONSIDERATIONS


 Administration/Storage

 Assessment/Interventions

OVERDOSAGE: SIGNS & SYMPTOMS
  Parenteral administration: Hypotension, asystole, chest pain, dyspnea, nausea, rash, pruritus

 Patient/Family Education

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Copyright
© 2003 Facts and Comparisons
David S. Tatro
A to Z Drug Facts