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LAVIE 500 MG 30 TAB
- Sku : I-027899
Key features
LAVIE 500 MG 30 TAB is a film-coated tablet formulation that contains levetiracetam 500 mg as the active ingredient. It works by binding to the synaptic vesicle protein SV2A, modulating neurotransmitter release and reducing neuronal hyperexcitability. It is indicated as adjunctive therapy for partial‑onset seizures in patients aged 1 month and older, for myoclonic seizures in patients aged 12 years and older with Juvenile Myoclonic Epilepsy, and for primary generalized tonic‑clonic seizures in patients aged 6 years and older with Idiopathic Generalized Epilepsy. Supplied as 500 mg film-coated tablets in a pack of 30.- Brand: LAVIE
- Active Ingredient: LEVETIRACETAM
- Strength: 500mg
- Dosage Form: Film-coated tablet
- Pack Size: 30 Tablets
- Route: Oral use
- Prescription Status: Prescription
- Therapeutic Class: Anticonvulsant
- Pharmacological Group: Antiepileptics
- Manufacturer: Jamjoom Pharmaceuticals Factory Company
- Country of Origin: Saudi Arabia
- SFDA Registration No.: 2809222658
- Shelf Life: 36 months
- Storage: store below 30°c
Indications
Approved Uses
Adjunctive therapy for partial-onset seizures in patients aged 1 month and older, myoclonic seizures in patients aged 12 years and older with Juvenile Myoclonic Epilepsy, and primary generalized tonic-clonic seizures in patients aged 6 years and older with Idiopathic Generalized Epilepsy.
Dosage & Administration
Dosing by Condition
Partial-onset seizures (adults): Initial 1000 mg/day (500 mg twice daily); increase by 1000 mg/day every 2 weeks; max 3000 mg/day. Juvenile myoclonic epilepsy (adults/adolescents ≥12 years): Initial 1000 mg/day (500 mg twice daily); increase by 1000 mg/day every 2 weeks; max 3000 mg/day. Primary generalized tonic-clonic seizures (adults): Initial 1000 mg/day (500 mg twice daily); increase by 1000 mg/day every 2 weeks; max 3000 mg/day.
Initial Dose
500 mg twice daily (1000 mg/day)
Maintenance Dose
1000 mg to 3000 mg per day, divided into two doses.
Maximum Dose
3000 mg per day.
Children's Dosage
Children 1 month to <6 months: 7 mg/kg twice daily (max 21 mg/kg twice daily). Children 6 months to <4 years: 10 mg/kg twice daily (max 25 mg/kg twice daily). Children 4 to <12 years: 10 mg/kg twice daily (max 30 mg/kg twice daily). Adolescents 12-17 years (≥50 kg): same as adult dosing
Dose Adjustment Notes
Renal dose adjustment is required based on creatinine clearance; no routine hepatic dose adjustment is needed, but in severe hepatic impairment with concomitant renal impairment, start at ~50% of the usual daily dose (because CrCl may be overestimated). Titration for IR tablets is typically in 500 mg increments.
How to Take
Swallow the film-coated tablet whole with water; may be taken with or without food; for immediate-release levetiracetam tablets, administer in 2 divided doses (typically twice daily) as prescribed.
Safety & Warnings
Contraindications
Hypersensitivity to levetiracetam or other pyrrolidone derivatives.
Warnings & Precautions
Key warnings/precautions: monitor for behavioral/psychiatric changes and suicidality; risk of serious hypersensitivity and severe skin reactions (SJS/TEN/DRESS); adjust dose in renal impairment; avoid abrupt discontinuation; consider monitoring for hematologic abnormalities if clinically indicated.
Age Restriction
Levetiracetam is approved from 1 month of age for certain seizure types; this 500 mg film‑coated tablet is generally appropriate only for patients (typically older children/adolescents/adults) who can safely swallow tablets-use oral solution in infants/young children.
Driving Warning
May Cause Drowsiness
Drug Interactions
Interaction Severity
Clinically most relevant interactions are additive CNS depression with alcohol and other sedatives (caution/avoid alcohol); levetiracetam has minimal clinically significant pharmacokinetic drug-drug interactions (no major CYP effects).
Food Interaction
No clinically significant food restriction; may be taken with or without food (food may delay Tmax but does not meaningfully reduce overall exposure).
Special Populations
Pregnancy
Consult Doctor
Breastfeeding
Caution
Children
Children 1 month to <6 months: 7 mg/kg twice daily (max 21 mg/kg twice daily). Children 6 months to <4 years: 10 mg/kg twice daily (max 25 mg/kg twice daily). Children 4 to <12 years: 10 mg/kg twice daily (max 30 mg/kg twice daily). Adolescents 12-17 years (≥50 kg): same as adult dosing
Elderly
Dose adjustment based on renal function (CrCl); start at lower end of dosing range and titrate carefully; monitor renal function regularly
Kidney Impairment
Dose adjust by creatinine clearance (adult immediate‑release): CrCl >80: 500-1500 mg q12h; CrCl 50-80: 500-1000 mg q12h; CrCl 30-50: 250-750 mg q12h; CrCl <30: 250-500 mg q12h; ESRD on dialysis: 500-1000 mg q24h plus 250-500 mg supplemental after dialysis.
Storage & Patient Advice
Patient Counseling
Take exactly as prescribed (typically twice daily for IR tablets) with or without food; swallow tablets whole; do not stop abruptly without medical advice; may cause dizziness/somnolence-avoid driving/machinery until effects are known; avoid or limit alcohol due to additive CNS effects; report mood/behavior changes or suicidal thoughts promptly; if a dose is missed, take when remembered unless near next dose-do not double.
Pharmacology
Duration of Effect
Immediate-release levetiracetam provides clinical coverage consistent with twice-daily dosing (about 12-hour dosing interval); elimination half-life is ~6-8 hours in adults with normal renal function.
Half-Life
Adults: ~6-8 hours (typical ~7 hours); children generally shorter (~5-7 hours, age-dependent).
Product Information
Available Dosage Forms
Levetiracetam is available as immediate-release tablets/film-coated tablets, oral solution, and IV formulations (solution for injection/infusion or concentrate depending on market); extended-release tablets also exist in some markets but are not the SFDA-listed dosage form for this product.
Composition per Dose
Each film-coated tablet: 500 mg levetiracetam
Generic Availability
Yes
OTC Alternatives
No OTC alternative
Legal Disclaimer - Al Mujtama Pharmacy
The product information provided is derived from verified pharmaceutical references and is intended for general health education only. It is not a substitute for professional medical advice, diagnosis, or treatment.
Al Mujtama Pharmacy assumes no legal or medical liability for:
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- Any discrepancy between the information provided and the product's package insert or SFDA guidelines
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