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PRODUCT DETAIL

Kineret 100 mg/0,67 ml injekčný roztok v naplnenej injekčnej striekačke

Code 8107A
MA number EU/1/02/203/006
Product Form: sol inj 7x0,67 ml /100 mg (striek.inj.napl.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 29 - ANTIRHEUMATICA, ANTIPHLOGISTICA, ANTIURATICA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L04 Immunosuppressants
L04A Immunosuppressants
L04AC Interleukin inhibitors
L04AC03 Anakinra
Shelf life: 36
Container: pre-filled syringe
Route of admin.: Subcutaneous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application
MA issued: 08.03.2002
SmPC + PL: European Medicines Agency's database
Dokument: DHPC_ KINERET(anakinra)-reklamácie lieku výskyt pevnej hmoty.pdf  
Dokument: Kineret_Príručka pre zdravotníckych pracovníkov.pdf  
Dokument: Kineret_Príručka pre pacienta.pdf  
Safety feature Yes
Data update: 18.06.2018
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