Levetiracetam
is accustomed for test of partial, myoclonic, and tonic-clonic seizures, and is
used off-label for berserk states and cephalalgia prophylaxis. Levetiracetam
has actual favorable pharmacokinetics with acceptable bioavailability and
accelerated accomplishment of abiding state. Its hepatic metabolism is basal
and nonoxidative, authoritative it safe for use with hepatic agitator inducers
or inhibitors. The above metabolite is a carboxylic acid derivate, which is
abeyant and accounts for almost one division of the administered dose.
Levetiracetam is excreted renally, with a beggarly half-life of 7 hours in
adults and hardly beneath than that in children. Renal dysfunction may
accreditation ameliorative ecology and/or dosage adjustment.
Given
the abridgement of biologic interactions and agreeably pharmacokinetics, the
primary uses for ameliorative biologic ecology of levetiracetam are
acquiescence affirmation and administration of physiological changes such as
puberty, pregnancy, and aging. Toxicities associated with levetiracetam use
cover decreased hematocrit and red claret corpuscle count, decreased neutrophil
count, somnolence, asthenia, and dizziness. These toxicities may be associated
with claret concentrations in the ameliorative range.
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