The HPRA advises healthcare professionals not to retain printed versions of Summary of Product Characteristics (SPC) documents. As these documents are subject to frequent content updates, including changes to safety and dose related information, we recommend that you visit our website as necessary to access the most up-to-date versions. If you have any queries about specific SPCs on our website then please e-mail info@hpra.ie


Reblozyl



Bristol-Myers Squibb Pharma EEIGEU/1/20/1452/002

Main Information

Trade NameReblozyl
Active SubstancesLuspatercept
Dosage FormPowder for solution for injection
Licence HolderBristol-Myers Squibb Pharma EEIG
Licence NumberEU/1/20/1452/002

Group Information

ATC CodeB03XA06 luspatercept

Status

License statusAuthorised
Licence Issued25/06/2020
Legal statusProduct subject to prescription which may not be renewed (A)
Supply StatusSupply through pharmacies only
Advertising StatusAdvertising to healthcare professionals only
Conditions of LicenceMedicinal product subject to restricted medical prescription (see Annex I: Summary of Product Characteristics, section 4.2).
Marketing StatusUnknown

Documents

Summary of Product CharacteristicsSearch EMA website
Package LeafletSearch EMA website
Public Assessment ReportSearch EMA website
« Back