Logufen

Logufen

levetiracetam

Manufacturer:

Kusum Healthcare

Distributor:

Kusum Healthcare
Concise Prescribing Info
Contents
Levetiracetam
Indications/Uses
Monotherapy for partial onset seizure. Adjunctive therapy for partial onset seizures, myoclonic seizures & primary generalized tonic-clonic seizures.
Dosage/Direction for Use
Monotherapy Adult & adolescent >16 yr 250 mg bid. To be increased to initial dose of 500 mg bid after 2 wk. May be further increased by 250 mg bid every 2 wk depending upon clinical response. Max: 1,500 mg bid. Add-on therapy Adult ≥18 yr & adolescent 12-17 yr weighing ≥50 kg Initially 500 mg bid. May be increased up to 1,500 mg bid. Change dose in 500 mg bid increases or decreases every 2-4 wk. Adolescent 12-17 yr & childn 6-11 yr weighing <50 kg Use the lowest effective dose. Initially 250 mg bid in childn or adolescent of 25 kg. Max: 750 mg bid. Renal impairment Adult & adolescent weighing >50 kg CrCl >80 mL/min/1.73 m2 500-1,500 mg bid, 50-79 mL/min/1.73 m2 500-1,000 mg bid, 30-49 mL/min/1.73 m2 250-750 mg bid, <30 mL/min/1.73 m2 250-500 mg bid; ESRD patients undergoing dialysis 500-1,000 mg once daily, w/ a 750-mg loading dose on the 1st day of treatment then a 250- to 500-mg supplemental dose following dialysis. Childn & adolescent weighing <50 kg CrCl >80 mL/min/1.73 m2 10-30 mg/kg bid, 50-79 mL/min/1.73 m2 10-20 mg/kg bid, 30-49 mL/min/1.73 m2 5-15 mg/kg, <30 mL/min/1.73 m2 5- 10 mg/kg bid; ESRD patients undergoing dialysis 10-20 mg/kg once daily, w/ a 15-mg/kg loading dose on the 1st day of treatment then a 5- to 10-mg/kg supplemental dose following dialysis. Severe hepatic impairment 50% reduction of daily maintenance dose when CrCl is <60 mL/min/1.73 m2.
Administration
May be taken with or without food.
Contraindications
Hypersensitivity to levetiracetam or other pyrrolidone derivatives.
Special Precautions
Monitor patients for signs of depression &/or suicidal ideation & behaviours & consider appropriate treatment. W/draw gradually if treatment should be discontinued. Minor or moderate influence on the ability to drive & use machines. Renal impairment. Not recommended during pregnancy & in women of childbearing potential not using contraception unless clinically necessary, & lactation. Childn & adolescent <16 yr as monotherapy. Not adapted for use in infants & childn <6 yr & childn weighing <25 kg for administration of doses <250 mg.
Adverse Reactions
Nasopharyngitis; somnolence, headache. Anorexia; depression, hostility/aggression, anxiety, insomnia, nervousness/irritability; convulsion, balance disorder, dizziness, lethargy, tremor; vertigo; cough; abdominal pain, diarrhoea, dyspepsia, vomiting, nausea; rash; asthenia/fatigue.
MIMS Class
Anticonvulsants
ATC Classification
N03AX14 - levetiracetam ; Belongs to the class of other antiepileptics.
Presentation/Packing
Form
Logufen FC tab 250 mg
Packing/Price
30's (P17/film-coated tab, P510/box)
Form
Logufen FC tab 500 mg
Packing/Price
30's (P990/box, P33/film-coated tab)
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