What is the use and dosage of Amantadine for influenza A and Parkinson's disease?

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Amantadine Use and Dosage for Influenza A and Parkinson's Disease

Amantadine is indicated for prophylaxis and treatment of influenza A virus infection, as well as for the treatment of Parkinson's disease and drug-induced extrapyramidal reactions, with specific dosing requirements for each indication based on patient age and renal function. 1

Influenza A

Prophylaxis and Treatment

  • Amantadine is effective for both prevention (70-90% effective) and treatment of influenza A virus infection 2
  • For treatment, amantadine should be started within 24-48 hours of symptom onset to reduce severity and duration of illness 2
  • Treatment should continue for 24-48 hours after symptoms disappear 2
  • For prophylaxis, amantadine should be continued for at least 10 days following known exposure 1

Adult Dosing for Influenza A

  • Standard adult dose: 200 mg daily (can be given as single dose or 100 mg twice daily) 1
  • For adults ≥65 years: 100 mg daily due to age-related decline in renal function 2
  • Split dosing (100 mg twice daily) may reduce CNS side effects 1

Pediatric Dosing for Influenza A

  • Children 1-9 years: 5 mg/kg/day (not to exceed 150 mg/day) 2
  • Children 10-12 years: 200 mg/day (100 mg twice daily) 2
  • For children weighing <40 kg: 5 mg/kg/day regardless of age 2

Parkinson's Disease

Adult Dosing for Parkinson's Disease

  • Initial dose: 100 mg twice daily when used alone 1
  • For patients with serious medical illnesses or those on other antiparkinson drugs: start with 100 mg daily 1
  • May increase to 300-400 mg daily in divided doses if needed, with close supervision 1
  • Onset of action typically within 48 hours 1

Concomitant Therapy

  • When used with levodopa: maintain amantadine at 100 mg once or twice daily while gradually increasing levodopa to optimal benefit 1
  • May help smooth out fluctuations in improvement seen with levodopa alone 1

Drug-Induced Extrapyramidal Reactions

  • Standard dose: 100 mg twice daily 1
  • May increase to 300 mg daily in divided doses if needed 1

Dosage Adjustments for Renal Impairment

Amantadine is primarily excreted unchanged in urine (90% of ingested dose) and requires dose adjustment in renal impairment 3, 4:

  • Creatinine clearance 30-50 mL/min: 200 mg first day, then 100 mg daily thereafter 1
  • Creatinine clearance 15-29 mL/min: 200 mg first day, then 100 mg on alternate days 1
  • Creatinine clearance <15 mL/min: 200 mg every 7 days 1
  • Hemodialysis patients: 200 mg every 7 days (hemodialysis removes <5% of the drug) 1, 3

Side Effects and Monitoring

Common Side Effects

  • CNS side effects (5-10% of patients): nervousness, insomnia, difficulty concentrating, lightheadedness 2
  • Gastrointestinal effects: anorexia, nausea 2
  • Side effects often diminish after the first week of use 2

Special Considerations

  • More serious CNS effects (confusion, seizures) occur primarily in elderly, those with renal disease, or seizure disorders 2
  • Elderly patients may experience more severe CNS side effects and higher incidence of dizziness and ataxia 2
  • Amantadine resistance can develop during treatment, so therapy should be limited to 3-5 days when possible 2, 5

Important Caveats

  • Amantadine is not a substitute for influenza vaccination 1
  • In Parkinson's disease, amantadine is less effective than levodopa 1
  • Patients may experience decreased effectiveness after a few months of use for Parkinson's disease; temporary discontinuation followed by reinitiation may restore benefit 1
  • Due to high levels of adamantane resistance among current influenza A strains, neuraminidase inhibitors (oseltamivir, zanamivir) may be preferred for influenza treatment in many regions 5
  • Amantadine has a large volume of distribution and can accumulate in patients with impaired renal function, potentially leading to toxicity 4

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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