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Primidone

OEM  OEM Services Provided
Feature Good stability
Classification Chemicals
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CategoryDetails
Chemical FormulaC₁₂H₁₈N₂O₃ (Barbiturate derivative)
Therapeutic ClassAnticonvulsant – Voltage-gated sodium channel blocker
Primary Indications– Partial seizures: Adjunctive therapy
– Generalized tonic-clonic seizures: Secondary prevention
– Essential tremor: First-line treatment
– Myoclonus: Symptomatic control
Pharmacodynamics– Metabolites: Active phenobarbital (80% conversion)
– Mechanism: Enhances GABA-ergic inhibition
– Onset: 1-2 weeks (therapeutic effect)
Pharmacokinetics– Bioavailability: ~100% (oral)
– Half-life: 12-16 hours
– Protein binding: 20-30%
– Excretion: Renal (metabolites)
Dosage Forms– Tablets: 50mg, 250mg
– Capsules: 250mg
– Oral suspension: 250mg/5mL
Standard Regimen– Adults: 125-250mg BID (max 2.5g/day)
– Elderly: Reduce by 50%
– Pediatrics: 25mg/kg/day divided TID
Adverse Effects– Common: Sedation, ataxia, nystagmus
– Severe: Stevens-Johnson syndrome (rare)
– Chronic: Osteomalacia (long-term use)
Drug Interactions– Enhanced effects: Alcohol, CNS depressants
– Reduced efficacy: Carbamazepine, phenytoin (enzyme induction)
– Monitoring required: Warfarin, oral contraceptives
Regulatory Status– FDA: Pregnancy Category D
– EMA: Requires risk-benefit assessment
– Generic availability: Multiple manufacturers (low-cost options)
Market Position– Declining use: Replaced by newer AEDs
– Niche applications: Essential tremor, refractory epilepsy
– Cost advantage: Affordable in resource-limited settings

Note: Requires therapeutic drug monitoring due to variable metabolism. Contraindicated in porphyria and severe hepatic impairment.

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Declaration: The products displayed on this website are intended exclusively for industrial applications or scientific research. They are not intended for medical, pharmaceutical, or food use. In accordance with applicable laws and regulations, purchasing organizations must hold valid qualifications and approvals.

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