FOSPHENYTOIN (CEREBYX)

Authors
Citation
Tr. Browne, FOSPHENYTOIN (CEREBYX), Clinical neuropharmacology, 20(1), 1997, pp. 1-12
Citations number
51
Categorie Soggetti
Clinical Neurology","Pharmacology & Pharmacy
Journal title
ISSN journal
03625664
Volume
20
Issue
1
Year of publication
1997
Pages
1 - 12
Database
ISI
SICI code
0362-5664(1997)20:1<1:F(>2.0.ZU;2-Y
Abstract
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.