GRASTOFIL

This brand name is authorized in Austria, Canada, Croatia, Estonia, France, Ireland, Italy, Lithuania, Poland.

Active ingredients

The drug GRASTOFIL contains one active pharmaceutical ingredient (API):

1
UNII PVI5M0M1GW - FILGRASTIM
 

Filgrastim causes marked increases in peripheral blood neutrophil counts within 24 hours, with minor increases in monocytes.

 
Read more about Filgrastim

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
L03AA02 Filgrastim L Antineoplastic and immunomodulating agents → L03 Immunostimulants → L03A Immunostimulants → L03AA Colony stimulating factors
Discover more medicines within L03AA02

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
CA Health Products and Food Branch 02441489, 02454548
EE Ravimiamet 1630448, 1630583, 1630594, 1630606
FR Base de données publique des médicaments 60169147, 62635483
IE Health Products Regulatory Authority 88184, 88188
IT Agenzia del Farmaco 043068016, 043068028, 043068030, 043068042
LT Valstybinė vaistų kontrolės tarnyba 1071754, 1071755, 1071756, 1071757
PL Rejestru Produktów Leczniczych 100157968, 100286022

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