Indications |
Oral Adjunct in partial seizures Adult: Initially, 500 mg bid on the 1st day. May increase in steps of 1 g at 2-4 wk intervals until effective antiepileptic control is achieved. Max: 3 g/day. Child: 4-15 yr (<50 kg): Initially 10 mg/kg bid. May be increased by 10 mg/kg bid at 2-wk intervals. Adolescents ≥16 yr or 50 kg initially 500 mg bid. May be increased by 500 mg bid at 2-4 wk intervals. Max: 60 mg/kg/day. Renal impairment: Suitable total daily dose (given as 2 divided doses) based on CrCl.
Oral Monotherapy for partial seizures with or without secondary generalisation Adult: Initially 500 mg daily, increased after 2 wk to 1 g daily. May further increase in steps of 500 mg at 2 wk intervals. Max: 3 g/day. Renal impairment: Suitable total daily dose (given as 2 divided doses) based on CrCl.
Intravenous Adjunct in partial seizures Adult: Initially, 500 mg bid on the 1st day. May increase in steps of 1 g at 2-4 wk intervals until effective antiepileptic control is achieved. Max: 3 g/day. No safety and efficacy data for IV usage >4 days. Child: 4-15 yr (<50 kg): Initially 10 mg/kg bid via IV infusion over 15 min. May be increased by 10 mg/kg bid at 2-wk intervals. Adolescents ≥16 yr or 50 kg initially 500mg bid via IV infusion over 15 min. May be increased by 500 mg bid at 2-4 wk intervals. Max: 60 mg/kg/day. Renal impairment: Suitable total daily dose (given as 2 divided doses) based on CrCl.
Intravenous Monotherapy for partial seizures with or without secondary generalisation Adult: Initially 500 mg daily, increased after 2 wk to 1 g daily. May further increase in steps of 500 mg at 2 wk intervals. Max: 3 g/day. No safety and efficacy data for IV usage >4 days. Renal impairment: Suitable total daily dose (given as 2 divided doses) based on CrCl.
Special Populations: Severe renal impairment (<30 mL/min): 250-500 mg bid. End-stage renal failure patients using dialysis: 500-1000 mg every 24 hr; a supplemental dose of 250-500 mg following dialysis is recommended. Reconstitution: Add 100 ml of suitable diluent to vial. Suitable diluents include sodium chloride (0.9%) injection; lactated Ringer's injection and dextrose 5% injection. |
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Warnings / Precautions |
Renal and hepatic impairment; pregnancy, lactation; patients undergoing haemodialysis. If psychotic symptoms (eg hallucination) and behavioural symptoms (eg agitation, anxiety) occur, reduce dosage. Abrupt withdrawal may result in increased seizure frequency. May impair ability to drive or operate machinery during initial therapy. | ||||||||||||||||||||||||||||||||
Adverse Reactions |
Somnolence, asthenia, dizziness, vertigo, depression, emotional instability, hostility, nervousness, ataxia, tremor, amnesia, headache, nausea, dyspepsia, diarrhoea, anorexia, rash, diplopia. | ||||||||||||||||||||||||||||||||
Mechanism of Actions |
Anticonvulsant used in the treatment of partial seizures. The precise mechanism of anticonvulsant effect is unknown. Onset: 1 hr Absorption: Rapidly and almost completely absorbed from GI tract. Distribution: Not significantly protein bound (<10%). Distributed in breast milk. Metabolism: Not extensively metabolised (24% into inactive metabolite); primarily by enzymatic hydrolysis. Excretion: Excreted in the urine as both unchanged drug (66%) and metabolites. Plasma half life of 6-8 hr. |
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Administration |
May be taken with or without food. (Oral soln should be diluted in a glass of water.) |
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Storage Conditions |
Intravenous: Once reconstituted store at 15-30°C and use within 24 hr. | ||||||||||||||||||||||||||||||||
ATC Classification |
N03AX14 - levetiracetam ; Belongs to the class of other antiepileptics. | ||||||||||||||||||||||||||||||||
Storage |
Intravenous: Once reconstituted store at 15-30°C and use within 24 hr. | ||||||||||||||||||||||||||||||||
Available As |
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Levetiracetam
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Levetiracetam Containing Brands
Levetiracetam is used in following diseases
Drug - Drug Interactions of Levetiracetam
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