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Zonisamide

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Zonisamide, Zonegran

  • See Also
  1. Anticonvulsant
  2. Seizure Disorder
  • Indications
  1. Adjunctive management of Partial Seizures
  2. Add to primary antiepileptic regimens
    1. Carbamazepine
    2. Phenytoin
    3. Valproate
  3. Other potential uses currently being researched
    1. Myoclonic Seizures
    2. Infantile Spasm
    3. Atypical Absence Seizure
    4. Generalized Tonic Clonic Seizures
  • Contraindications
  1. Sulfonamide Allergy
  2. Pregnancy (Teratogenic in animals)
  • Mechanism
  1. Anticonvulsant
  2. Sulfonamide derivative
  3. Blocks CNS Sodium and Calcium channels and stabilizes Neuron membranes, preventing hypersynchronization
  4. Also binds GABA Receptor ionophore complex, but does not appear to potentiate GABA activity at Synapse
  5. Facilitates the Neurotransmitters Dopamine and Serotonin
  • Dosing
  • Adults (and age >16 years)
  1. Initial: 100 mg orally daily for at least 2 weeks
  2. Increase: 100 mg every two weeks as needed
  3. Target: 400 mg/day divided once to twice daily
  4. Maximum: 600 mg/day (but doses above 400 mg/day do not appear to offer benefit)
  5. Caution: Increase more slowly in Renal Insufficiency and hepatic dysfunction
  • Pharmacokinetics
  1. Weak carbonic anhydrase inhibitor
  2. Sulfonamide that blocks Sodium and Calcium channels
    1. Increases Dopaminergic transmission
    2. Increases serotonergic transmission
  3. Metabolized by CYP3A4
    1. Drug levels affected by Phenytoin, Carbamazepine, Phenobarbital, Valproic Acid
  4. Half-Life: 60 hours
  • Drug Interactions
  1. Increased Zonisamide clearance with CYP3A4 inducers
    1. Phenytoin
    2. Carbamazepine
    3. Phenobarbital
  2. Concurrent carbonic anhydrase inhibitor (Topamax)
    1. Increased Nephrolithiasis risk
  • Adverse effects
  1. Common
    1. Dizziness
    2. Ataxia
    3. Somnolence
    4. Nausea
    5. Anorexia
    6. Abdominal Pain
    7. Insomnia
    8. Impaired cognition
      1. Confusion
      2. Decreased concentration
      3. Speech problems
  2. Serious
    1. Psychosis
    2. Stevens Johnson Syndrome
    3. Toxic Epidermal Necrolysis
    4. Fulminant hepatic necrosis
    5. Narrow Angle Glaucoma (IOP may increase during first month of use)
  3. Childhood Adverse Effects
    1. Oligohydrosis
    2. Hyperthermia (and Heat Stroke)
  4. Other
    1. Nephrolithiasis (associated with Metabolic Acidosis)
  • Safety
  1. Unknown Safety in Pregnancy (but Teratogenic in animals)
  2. Unknown Safety in Lactation