This brand name is authorized in Austria, Cyprus, Estonia, Spain, Finland, France, Croatia, Ireland, Italy, Lithuania, Romania, United States

Active ingredients

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

1 RSV glycoprotein F antigen

RSV glycoprotein F antigen is designed to enhance antigen-specific cellular immune response and neutralizing antibodies response in individuals with pre-existing immunity against RSV. The adjuvant AS01E facilitates the recruitment and activation of antigen presenting cells carrying vaccine-derived antigens in the draining lymph node, which in turn leads to the generation of RSVPreF3-specific CD4+ T cells.

Read about RSV glycoprotein F antigen

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
ABRYSVO Powder and solvent for 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
J07BX05 J Antiinfectives for systemic use → J07 Vaccines → J07B Viral vaccines → J07BX Other viral vaccines
Discover more medicines within J07BX05

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: EE Ravimiamet Identifier(s): 3044618, 3044629, 3044630
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 1231752001
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 587002
Country: FR Base de données publique des médicaments Identifier(s): 60990140
Country: IT Agenzia del Farmaco Identifier(s): 050831015, 050831027, 050831039, 050831041, 050831054, 050831066
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1097701, 1097702, 1097703, 1097704, 1097705, 1097706
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W69758001, W69758002, W69758003, W69758004, W69758005, W69758006
Country: US FDA, National Drug Code Identifier(s): 0069-0207, 0069-0250, 0069-0344

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