This brand name is authorized in Austria, Brazil, Canada, Cyprus, Ecuador, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Israel, Japan, Lithuania, Nigeria, Netherlands, New Zealand, Poland, Romania, Singapore, Tunisia, United Kingdom, United States, South Africa
The drug AVASTIN contains one active pharmaceutical ingredient (API):
1
Bevacizumab
UNII 2S9ZZM9Q9V - BEVACIZUMAB
|
Bevacizumab binds to vascular endothelial growth factor (VEGF), the key driver of vasculogenesis and angiogenesis, and thereby inhibits the binding of VEGF to its receptors, Flt-1 (VEGFR-1) and KDR (VEGFR-2), on the surface of endothelial cells. Neutralising the biological activity of VEGF regresses the vascularisation of tumours, normalises remaining tumour vasculature, and inhibits the formation of new tumour vasculature, thereby inhibiting tumour growth. |
Below package inserts are available for further reading:
Title | Information Source | Document Type | |
---|---|---|---|
AVASTIN Concentrate for solution for infusion | 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 |
---|---|---|
L01FG01 | Bevacizumab | L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01F Monoclonal antibodies and antibody drug conjugates → L01FG VEGF/VEGFR (Vascular Endothelial Growth Factor) inhibitors |
This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
---|---|---|
Country: BR | Câmara de Regulação do Mercado de Medicamentos | Identifier(s): 529207901139218, 529207902151211 |
Country: CA | Health Products and Food Branch | Identifier(s): 02270994 |
Country: EC | Agencia Nacional de Regulación, Control y Vigilancia Sanitaria | Identifier(s): 28761-02-09 |
Country: EE | Ravimiamet | Identifier(s): 1179952, 1187973 |
Country: ES | Centro de información online de medicamentos de la AEMPS | Identifier(s): 04300001, 04300002 |
Country: FI | Lääkealan turvallisuus- ja kehittämiskeskus | Identifier(s): 019445, 019781 |
Country: FR | Base de données publique des médicaments | Identifier(s): 60391646 |
Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 91527, 91530 |
Country: HK | Department of Health Drug Office | Identifier(s): 56637, 56638, 59449, 59450 |
Country: IL | מִשְׂרַד הַבְּרִיאוּת | Identifier(s): 4932, 4933 |
Country: JP | 医薬品医療機器総合機構 | Identifier(s): 4291413A1022, 4291413A2029 |
Country: LT | Valstybinė vaistų kontrolės tarnyba | Identifier(s): 1027602, 1027603 |
Country: NG | Registered Drug Product Database | Identifier(s): A6-0123 |
Country: NL | Z-Index G-Standaard | Identifier(s): 15023753 |
Country: NL | Z-Index G-Standaard, PRK | Identifier(s): 76910, 76929 |
Country: NZ | Medicines and Medical Devices Safety Authority | Identifier(s): 11531 |
Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100129386 |
Country: RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | Identifier(s): W64373001, W64373002 |
Country: SG | Health Sciences Authority | Identifier(s): 13065P, 14097P |
Country: TN | Direction de la Pharmacie et du Médicament | Identifier(s): 6993191H, 6993192H |
Country: US | FDA, National Drug Code | Identifier(s): 50242-060, 50242-061 |
Country: ZA | Health Products Regulatory Authority | Identifier(s): A39/26/0314, A39/26/0315 |
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