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🇪🇺EU · EMAApplication withdrawnATC: L04AA27

Fingolimod Mylan(fingolimod hydrochloride)

Multiple Sclerosis, Relapsing-Remitting

Marketing Authorisation Holder: Mylan Ireland Limited

EMA Authorisation: 18/08/2021

INN: fingolimod

Indication

Indicated as single disease modifying therapy in highly active relapsing remitting multiple sclerosis for the following groups of adult and paediatric patients aged 10 years and older: Patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (for exceptions and information about washout periods see sections 4.4 and 5.1) or Patients with rapidly evolving severe relapsing remitting multiple sclerosis defined by 2 or more disabling relapses in one year, and with 1 or more Gadolinium enhancing lesions on brain MRI or a significant increase in T2 lesion load as compared to a previous recent MRI.

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.