Vanflyta

Country: European Union

Language: Polish

Source: EMA (European Medicines Agency)

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Active ingredient:

quizartinib дигидрохлорид

Available from:

Daiichi Sankyo Europe GmbH

ATC code:

L01XE

INN (International Name):

quizartinib

Therapeutic group:

Środki przeciwnowotworowe

Therapeutic area:

Białaczka, szpikowe, ostre

Therapeutic indications:

Leczenie ostrej białaczki szpikowej.

Authorization status:

Odmówił

Documents in other languages

Public Assessment Report Public Assessment Report Bulgarian 06-01-2020
Public Assessment Report Public Assessment Report Spanish 06-01-2020
Public Assessment Report Public Assessment Report Czech 06-01-2020
Public Assessment Report Public Assessment Report Danish 06-01-2020
Public Assessment Report Public Assessment Report German 06-01-2020
Public Assessment Report Public Assessment Report Estonian 06-01-2020
Public Assessment Report Public Assessment Report Greek 06-01-2020
Public Assessment Report Public Assessment Report English 06-01-2020
Public Assessment Report Public Assessment Report French 06-01-2020
Public Assessment Report Public Assessment Report Italian 06-01-2020
Public Assessment Report Public Assessment Report Latvian 06-01-2020
Public Assessment Report Public Assessment Report Lithuanian 06-01-2020
Public Assessment Report Public Assessment Report Hungarian 06-01-2020
Public Assessment Report Public Assessment Report Maltese 06-01-2020
Public Assessment Report Public Assessment Report Dutch 06-01-2020
Public Assessment Report Public Assessment Report Portuguese 06-01-2020
Public Assessment Report Public Assessment Report Romanian 06-01-2020
Public Assessment Report Public Assessment Report Slovak 06-01-2020
Public Assessment Report Public Assessment Report Slovenian 06-01-2020
Public Assessment Report Public Assessment Report Finnish 06-01-2020
Public Assessment Report Public Assessment Report Swedish 06-01-2020
Public Assessment Report Public Assessment Report Croatian 06-01-2020

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