Prognia
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🇪🇺EU · EMAAuthorisedATC: L03AA13

Fulphila(pegfilgrastim)

Marketing Authorisation Holder: Biosimilar Collaborations Ireland Limited

EMA Authorisation: 20/11/2018

INN: pegfilgrastim

Indication

Reduction in the duration of neutropenia and the incidence of febrile neutropenia in adult patients treated with cytotoxic chemotherapy for malignancy (with the exception of chronic myeloid leukaemia and myelodysplastic syndromes).

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.