Ingestion of long-acting anticoagulant rodenticides such as brodifacoum can
lead to prolonged and life-threatening coagulopathy. A paucity of conflict
ing information is available on brodifacoum's half-life and elimination pha
rmacokinetics. In addition, the optimal dose, duration, and route of admini
stration of vitamin K-1 therapy are unknown. We report the case of a 52-yea
r-old man who ingested eight 43-g boxes of a rodenticide (d-Con Mouse-Prufe
II; 0.005% brodifacoum; Reckitt & Colman, Wayne, NJ). This case demonstrat
es that after stabilization with fresh frozen plasma, high-dose oral vitami
n K-1 therapy (congruent to 7 mg/kg per 24 hours divided every 6 hours) was
effective in treating brodifacoum-induced coagulopathy. The concentration
of vitamin K-1 required for normal coagulation in this case was less than t
he accepted value of 1 mu g/mL, which is derived from a rabbit model. In th
is case, brodifacoum appears to follow zero-order elimination pharmacokinet
ics. In future cases of patients with ingestions of long-acting anticoagula
nts who present with coagulopathy, it may be useful to obtain serial brodif
acoum concentrations to determine elimination curves to help predict the du
ration of oral vitamin K-1 therapy.