Name: | etiracetam, S-isomer |
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Name (isomeric): | DB01202 |
Drug Type: | small molecule |
Synonyms: |
Levetiracetamum [INN-Latin]; Levitiracetam; Levetiracetam [INN]
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Brand: | Keppra |
Category: | Nootropic Agents, Anticonvulsants |
CAS number: | 102767-28-2 |
Indication: | Used as adjunctive therapy in the treatment of partial onset seizures in adults and children 4 years of age and older with epilepsy. |
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Mechanism of Action: |
The precise mechanism(s) by which levetiracetam exerts its antiepileptic effect is unknown. The antiepileptic activity of levetiracetam was assessed in a number of animal models of epileptic seizures. Levetiracetam did not inhibit single seizures induced by maximal stimulation with electrical current or different chemoconvulsants and showed only mi...
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Absorption: | Rapidly and almost completely absorbed after oral administration (99%). Peak plasma concentrations occurring in about an hour following oral administration in fasted subjects. |
Protein binding: | Very low (<10%) |
Biotransformation: | The major metabolic pathway of levetiracetam (24% of dose) is an enzymatic hydrolysis of the acetamide group. No CYP450 metabolism detected. |
Route of elimination: | Sixty-six percent (66%) of the dose is renally excreted unchanged. The metabolites have no known pharmacological activity and are renally excreted. The mechanism of excretion is glomerular filtration with subsequent partial tubular reabsorption. |
Half Life: | 6-8 hours |
Clearance: | 0.96 mL/min/kg |
Toxicity: | Side effects include aggression, agitation, coma, drowsiness, reduced consciousness, slowed breathing |
Affected organisms: | Humans and other mammals |
Food interaction: |
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Drug interaction: |
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