Fosphenytoin is a phosphate ester prodrug of phenytoin developed as a
replacement for standard injectable sodium phenytoin. After absorption
, phenytoin is cleaved (conversion half-life 8-15 min) from fosphenyto
in. Unlike phenytoin, fosphenytoin is freely soluble in aqueous soluti
ons (including standard intravenous solutions) and rapidly absorbed by
the intramuscular route. Fosphenytoin has been tested successfully fo
r three indications in humans: intramuscular maintenance dosing, intra
muscular loading dose administration, and intravenous treatment of sta
tus epilepticus. Local toxicity (pain, burning, itching) is less by th
e intramuscular or intravenous route for fosphenytoin than for standar
d injectable sodium phenytoin. Systemic toxicity is similar with both
preparations except that hypotension is less common and paresthesias a
re more common with fosphenytoin.