Dalfampridine/ Fampridine (Fampyra) - Uses, Dose, Side effects, MOA

A potassium channel blocker called dalfampridine (Fampyra) enhances neuronal conduction in demyelinated axons. It helps individuals with multiple sclerosis become more mobile while walking.

Dalfampridine (Fampyra)  Uses:

  • It is intended to help patients with multiple sclerosis walk more easily.

Dalfampridine (Fampyra) Dose in Adults

Dalfampridine (Fampyra) Dose in the treatment of Multiple sclerosis:

  • 10 mg orally twice daily.
  • The maximum daily dose is 20 mg.
  • Exceeding 20 mg may not confer additional benefits.
  • Missed doses:
    • An additional dose or double dose shouldn't be given if a dose is missed.

Use in Children:

Not indicated.

Pregnancy Risk Factor C

  • Its use in pregnancy is not well-documented.

Use of Dalfampridine while breastfeeding

  • It is unknown if the drug will be excreted into breastmilk.
  • Experts recommend that you avoid breastfeeding while you are undergoing treatment, until more information is available.
  • Because of possible adverse effects in breastfeeding infants, the manufacturer suggests that you either stop using the drug or breastfeed.

Dalfampridine (Fampyra) Dose in Kidney Disease:

Notice:The Cockcroft-Gault formula calculates creatinine clearance.

  • The US labeling system:

    • Mild renal impairment (CrCl 51 - 80 mL/minute).
      • Although the manufacturer has not suggested any changes in the dosage, seizures could increase due to the reduced clearance.
    • Moderate-to-severe kidney impairment (CrCl = 50 mL/minute).
      • Contraindicated
  • Canadian labeling

    • Mild to severe impairment (CrCl ==80 mL/minute).
      • Contraindicated

Dose in Liver disease:

  • Adjustment in the dose is not required in patients with liver disease.
  • The drug undergoes minimal metabolism and is primarily excreted in urine as unchanged.

Common Side Effects of Dalfampridine (Fampyra):

  • Genitourinary:

    • Urinary tract infection

Less Common Side Effects of Dalfampridine (Fampyra):

  • Central nervous system:

    • Insomnia
    • Dizziness
    • Headache
    • Equilibrium disturbance
    • Paresthesia
  • Gastrointestinal:

    • Nausea
    • Constipation
    • Dyspepsia
  • Neuromuscular & skeletal:

    • Weakness
    • Back pain
    • Acute exacerbations of multiple sclerosis
  • Respiratory:

    • Nasopharyngitis
    • Pharyngolaryngeal pain

Contraindications to Dalfampridine (Fampyra):

  • allergy to 4-aminopyridine, dalfampridine, or any other formulation ingredient
  • History of Fits;
  • Moderate to severe renal impairment (CrCl >=50 mL/minute).

Additional contraindications to Canadian labeling

  • Mild, moderate or severe renal impairment (CrCl >=80 mL/minute);
  • Use of other forms or compounded 4-aminopyridines in conjunction with fampridine
  • Use with medication that inhibits the organic cationtransporter 2 (e.g. , cimetidine, or quinidine)

Warnings and precautions

  • Anaphylaxis

    • This drug can cause severe allergic reactions, including anaphylactic reactions.
    • Patients might present with symptoms such as urticaria, oropharyngeal, or laryngeal edema and angioedema (throat, tongue).
    • It is important to stop all treatment immediately and start the appropriate treatment such as Epinephrine.
  • Seizures

    • Seizures are a frequent adverse reaction to medication, particularly if you take greater doses.
    • The onset of seizures can happen right away during treatment or take weeks.
    • Seizures are more likely to occur in patients who have a history of seizures.
    • Treatment must be stopped if the patient has seizures.
    • Patients who have had seizures in the past should not take this drug.
    • It's critical to evaluate the risk of having seizures before starting treatment.
  • Infection of the urinary tract:

    • Clinical trials showed that the prevalence of urinary tract infections in patients with the placebo was higher than the placebo.
    • Patients with symptoms of the lower urinary tract must be evaluated.
  • Renal impairment

    • Patients with pre-existing kidney disease are more likely to experience seizures and other medication side effects, particularly neurological ones.
    • Mostly unmodified, it is eliminated by the kidneys.
    • It is contraindicated for mild, moderate, and severe renal impairment as well as other impairments, according to US medication labelling.

Dalfampridine (fampridine): Drug Interaction

Note: Drug Interaction Categories:

  • Risk Factor C: Monitor When Using Combination
  • Risk Factor D: Consider Treatment Modification
  • Risk Factor X: Avoid Concomitant Use

Risk Factor C (Monitor therapy).

Cimetidine May increase serum levels of Dalfampridine. Management: There are many differences in international recommendations regarding the concomitant administration of dalfampridine (also known as fampridine here in Canada) or cimetidine. Refer to appropriate product labeling.
MetFORMIN May increase serum levels of Dalfampridine. MetFORMIN may be increased by Dalfampridine.
QuiNIDine Dalfampridine serum levels could rise. Management: The concurrent administration of quinidine or dalfampridine, which are also known as fampridine in Canada, is not recommended in all international guidelines. Consult the relevant product labelling.

Monitoring parameters:

  • Renal function 
  • Monitor EEG
  • Monitor for the ability of the patient to walk.

How to administer Dalfampridine (Fampyra)?

  • It may be administered with or without food.
  • The drug should not be chewed, crushed, dissolved in liquids, or divided.

Mechanism of action of Dalfampridine (Fampyra):

  • Motor function is improved by the drug acting as a non-specific potentiochannel blocker. 
  • The potassium current blocker prolongs the action potential, delays repolarization, and improves nerve conduction in focally demyelinated Axons.
  • A decrease in neuronal conduction can improve the neurological motor function through the strengthening of the skeletal muscle fiber twist activity.

Absorption:

  • Rapid and complete

Protein binding:

  • It has only weakly-bound plasma proteins.

Metabolism:

  • The drug undergoes minimal metabolism.
  • In vitro data suggests the drug is metabolized in the liver primarily via CYP2E1 to 3-hydroxy-4aminopyridine. It is then further conjugated to 3-hydroxy-4-aminopyridine sulfate. The metabolites are inactive.

Bioavailability:

  • 96%

Half-life elimination:

  • 5.2-6.5 hours;

Time to peak plasma concentration:

  • 3-4 hours

Excretion:

  • Urine (96%; 90% of total dose as unchanged drug);
  • feces (0.5%)

International Brand Names of Dalfampridine:

  • Ampyra
  • Fampyra
  • Fampyra SR

Dalfampridine Brand Names in Pakistan:

No Brands Available in Pakistan.