Pharm

Lamotrigine

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Lamotrigine, Lamictal

  • Indications
  • Mechanism
  1. Phenyltriazine anticonvulsant (broad spectrum) indicated in both generalized and Focal Seizures
  2. Enhances Gamma-Aminobutyric Acid (GABA) inhibitory activity
  3. Other effects
    1. Reduce pain transmission
    2. Inhibits voltage-gated Sodium channels (see toxicity below)
    3. Suppresses Glutamate release
    4. Inhibits Serotonin reuptake
    5. Inhibits MAO reuptake
  • Pharmacokinetics
  1. Oral Bioavailability: 98%
  2. Elimination Half-Life: 22 to 36 hours
  3. Peak Activity (extended in Overdose)
    1. Immediate Release: 2 hours after ingestion
    2. Extended Release: 6 hours after ingestion
  4. Metabolism
    1. Glucuronidation (slowed in Gilbert Syndrome, and with Valproic Acid)
    2. Elimination in the urine
    3. No active metabolites
  • Adverse Effects
  • Serious
  1. Serious skin rash
    1. DRESS Syndrome
    2. Stevens Johnson Syndrome or Toxic Epidermal Necrolysis
      1. Onset in first 2 to 8 weeks after starting medication
      2. Incidence 0.3% in adults, 0.8% in children)
      3. Higher risk when combined with Valproic Acid
  2. Prolonged QRS Interval
    1. Increased risk of ventricular Arrhythmia or Cardiac Arrest
    2. Mechanism
      1. Sodium Channel Blocker
    3. Higher risk in underlying heart disease
      1. Coronary Artery Disease (prior Myocardial Infarction)
      2. Structural heart disease
      3. Atrioventricular Block
      4. Heart Failure
    4. Approach
      1. Avoid in high risk cardiovascular patients
      2. Consider baseline EKG in age over 60 years or Cardiovascular Risk Factors
      3. Avoid combining with other Sodium Channel Blockers
    5. References
      1. (2021) Presc Lett 28(6):34
  3. Aplastic Anemia
  4. Thrombocytopenia
  5. Neutropenia
  6. Pancytopenia
  7. Aseptic Meningitis
  8. Serotonin Syndrome
  • Drug Interactions
  1. Valproic Acid
    1. Slows Lamotrigine Glucuronidation
    2. Requires a decrease in Lamotrigine dose
  2. Enzyme-Inducing Anticonvulsants (require an increase in Lamotrigine dose)
    1. Carbamazepine
    2. Phenytoin
    3. Phenobarbital
    4. Primidone
  3. Oral Contraceptives
    1. Requires an increase in Lamotrigine dose to as much as double
  4. Other Interactions
    1. Rifampin
  • Precautions
  1. Slow titration over 6 weeks or more reduces the risk of Stevens-Johnson Syndrome
  2. Dosing adjustments are needed when used with agents listed under Drug Interactions
  3. Decrease dose by 25% in moderate to severe hepatic Impairment (50% if Ascites present)
  • Dosing
  • Adults (age > 12 years)
  1. Immediate Release
    1. Initial: 25 mg orally daily for 2 weeks
    2. Next: 50 mg orally daily for 2 weeks
    3. Next: Titrate dose by 50 mg/day divided twice daily every 1 to 2 weeks
    4. Typical dose: 225 to 375 mg/day divided orally twice daily
    5. Maximum dose: 400 mg/day divided twice daily
  2. Extended Release
    1. Initial: 25 mg orally daily for 2 weeks
    2. Next: 50 mg orally daily for 2 weeks
    3. Next: 100 mg orally daily for 1 week
    4. Next: Titrate dose by 50 mg/day taken daily every 1 week
    5. Typical dose: 300 to 400 mg/day orally daily
  3. Dose Adjustment when combined with a non-Valproic Acid, enzyme-inducing anticonvulsant drug or Oral Contraceptives
    1. Immediate Release Maximum Dose: 300 to 500 mg/day divided twice daily
    2. Extended Release Maximum Dose: 400 to 600 mg/day
  4. Dose Adjustment when combined with Valproic Acid
    1. Immediate Release
      1. Initial: 25 mg orally every other day for 2 weeks
      2. Next: 25 mg orally daily for 2 weeks
      3. Next: Titrate dose by 25 to 50 mg/day daily or divided twice daily every 1 to 2 weeks
      4. Typical dose: 100 to 200 mg/day daily or divided orally twice daily
    2. Extended Release
      1. Initial: 25 mg orally every other day for 2 weeks
      2. Next: 25 mg orally daily for 2 weeks
      3. Next: 50 mg orally daily for 1 week
      4. Next: Titrate dose by 25 to 50 mg/day daily or divided twice daily every 1 to 2 weeks
      5. Typical dose: 200 to 250 mg orally daily
  • Dosing
  • Children (age 2 to 12 years)
  1. Immediate Release
    1. Start: 0.3 mg/kg/day divided orally daily to twice daily for 2 weeks
    2. Next: 0.6 mg/kg/day divided orally daily to twice daily for 2 weeks
    3. Next: Titrate dose by 0.6 mg/kg/day divided twice daily every 1 to 2 weeks
    4. Typical dose: 4.5 to 7.5 mg/kg/day divided orally twice daily
    5. Maximum dose: 300 mg/day divided twice daily
  2. Dose Adjustment when combined with a non-Valproic Acid, enzyme-inducing anticonvulsant drug
    1. Start: 0.6 mg/kg/day divided orally daily to twice daily for 2 weeks
    2. Next: 1.2 mg/kg/day divided orally daily to twice daily for 2 weeks
    3. Next: Titrate dose by 1.2 mg/kg/day divided twice daily every 1 to 2 weeks
    4. Typical dose: 5 to 15 mg/kg/day divided orally twice daily
    5. Maximum dose: 400 mg/day divided twice daily
  3. Dose Adjustment when combined with Valproic Acid
    1. Start: 0.15 mg/kg/day divided orally daily to twice daily for 2 weeks
    2. Next: 0.3 mg/kg/day divided orally daily to twice daily for 2 weeks
    3. Next: Titrate dose by 0.3 mg/kg/day divided twice daily every 1 to 2 weeks
    4. Typical dose: 1 to 3 mg/kg/day divided orally twice daily
    5. Maximum dose: 200 mg/day divided twice daily
  • Monitoring
  1. Obtain labs monthly for the first 2 months and then every 3 to 12 months
  2. Complete Blood Count
  3. Liver Function Test
  • Safety
  1. Pregnancy Category C
    1. Risk of Cleft Lip and Palate
    2. No increase in Autism risk
      1. Hernandez-Diaz (2024) N Engl J Med 390(12):1069-79 +PMID: 38507750 [PubMed]
  2. Avoid in Lactation
    1. Risk of apnea, drowsiness and poor feeding
  • References
  1. (2022) Presc Lett, Resource #361206, Antiseizure Medications
  2. Olson (2020) Clinical Pharmacology, Medmaster Miami, p. 56-7
  3. Hamilton (2020) Tarascon Pocket Pharmacopoeia