SKYRIZI

This brand name is authorized in Austria, Australia, Brazil, Canada, Ecuador, Estonia, Spain, Finland, France, Hong Kong, Ireland, Israel, Japan, Lithuania, Netherlands, New Zealand, Poland, Romania, Turkey, United Kingdom

Active ingredients

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

1 Risankizumab
UNII 90ZX3Q3FR7 - RISANKIZUMAB

Risankizumab is a humanised immunoglobulin G1 (IgG1) monoclonal antibody that selectively binds with high affinity to the p19 subunit of human interleukin 23 (IL-23) cytokine and inhibits IL-23-dependent cell signalling and release of proinflammatory cytokines. Risankizumab is indicated for the treatment of moderate to severe plaque psoriasis.

Read about Risankizumab

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
SKYRIZI Solution for injection European Medicines Agency (EU) MPI, EU: SmPC

Medicine classification

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

ATC code Group title Classification
L04AC18 L Antineoplastic and immunomodulating agents → L04 Immunosuppressants → L04A Immunosuppressants → L04AC Interleukin inhibitors
Discover more medicines within L04AC18

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: AU Pharmaceutical Benefits Scheme Identifier(s): 11827L, 11858D
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 543719110004107
Country: CA Health Products and Food Branch Identifier(s): 02487454
Country: EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria Identifier(s): 174-MBE-0121, 235-MBE-0822
Country: EE Ravimiamet Identifier(s): 1794102, 1848416, 1848427, 1848438
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 1191361001
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 055240, 409325, 557887
Country: FR Base de données publique des médicaments Identifier(s): 67060271
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 371219, 397916, 397922
Country: HK Department of Health Drug Office Identifier(s): 66488
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 9258, 9259, 9314, 9315
Country: JP 医薬品医療機器総合機構 Identifier(s): 3999450A1025, 3999450G1028, 3999450G2024, 3999450G3020, 3999450G4027
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1087673, 1092291, 1092292
Country: NL Z-Index G-Standaard, PRK Identifier(s): 197629
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 20126, 21860, 21949
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100417814, 100461473
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W66053001, W67699001, W67700001, W69348001, W69349001
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8680656080520, 8680656080599, 8680656080605

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