REMS
Absorption: Well absorbed following oral or SUBQ administration. Oral absorption requires presence of bile salts. Some vitamin K is produced by bacteria in the GI tract.
Distribution: Unknown.
Half-Life: Unknown.
| ROUTE | ONSET | PEAK‡ | DURATION‡ |
|---|---|---|---|
| PO | 612 hr | unknown | unknown |
| SUBQ | 12 hr | 36 hr | 1214 hr |
| IV | 12 hr | 36 hr | 12 hr |
‡Control of hemorrhage.
‡Normal PT achieved.
Contraindicated in:
Use Cautiously in:
Exercise Extreme Caution in:
Derm: eczematous reactions, flushing, kernicterus, rash, scleroderma-like lesions, urticaria
GI: gastric upset, hyperbilirubinemia (large doses in very premature infants), unusual taste
Hemat: hemolytic anemia
Local: erythema, pain at injection site, swelling
Drug-drug:
IV use of phytonadione should be reserved for patients with serious or life-threatening bleeding and elevated INR. Oral route is preferred in patients with elevated INRs and no serious or life-threatening bleeding. IM route should generally be avoided because of risk of hematoma formation.
Treatment of Hypoprothrombinemia Due to Vitamin K Deficiency (From Factors Other Than Warfarin)
Vitamin K Deficiency (Supratherapeutic INR) Secondary to Warfarin
Prevention of Hypoprothrombinemia During Total Parenteral Nutrition
Prevention of Vitamin KDeficiency Bleeding in Neonates
Treatment of Vitamin KDeficiency Bleeding in Neonates
Lab Test Considerations:
Fatal hypersensitivity reactions, including anaphylaxis, have occurred during and immediately after IV and IM injection of phytonadione.
IV Administration: