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