How it works: Treating relapses and symptoms →

Fampyra

EU: Approved in the EU since 2011US: FDA approved 2010

Other names
fampridine
Molecule type
Small molecule
Mechanism (ChEMBL)
Voltage-gated potassium channel blocker
Targets
Voltage-gated potassium channel
Availability
Authorised in all EU and EEA countries. Reimbursement is decided by each country.

Approvals

  • USAmpyra · Approved22 January 2010 Source
  • EU/EEAFampyra · Authorised20 July 2011 Source
  • EU/EEAFampridine Accord · Authorised · Generic24 September 2020 Source

Safety communications

None recorded.

Most-reported side effects (FDA reports)

Reports to the FDA's adverse event system (FAERS) show what people and doctors reported while taking the medicine. They do not prove the medicine caused it, and they are not rates.

74,058 reports in total, 21,758 marked serious.

  • Gait disturbance11,184
  • Drug ineffective8,493
  • Fall7,624
  • Fatigue5,692
  • Balance disorder5,007
  • Multiple sclerosis relapse4,899
  • Therapy cessation4,619
  • Dizziness4,138
  • Urinary tract infection3,885
  • Asthenia3,600

Trials

Key trials

Large trials with a reported result on their main goal.

Running now

Other trials (36)

Completed small trials, dose-finding studies and trials in other diseases.

For information only, not medical advice. Talk to your neurologist before changing treatment.

Hypotheses involving this medicine

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Lab studies

Lab studies in animals or cells. Results in animals often do not hold in people, and these studies never change the status of an idea.

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