WAYLIVRA

This brand name is authorized in Austria, Croatia, Estonia, France, Ireland, Italy, Lithuania, Poland, Romania, UK.

Active ingredients

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

1
UNII 6JON30SLDT - VOLANESORSEN SODIUM
 

Volanesorsen is an antisense oligonucleotide designed to inhibit the formation of apoC-III, a protein that is recognised to regulate both triglyceride metabolism and hepatic clearance of chylomicrons and other triglyceride-rich lipoproteins.

 
Read more about Volanesorsen

Medication package inserts

Below package inserts are available for further reading:

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

Medicine classification

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

ATC Group Classification
C10AX Other lipid modifying agents C Cardiovascular system → C10 Lipid modifying agents → C10A Lipid modifying agents, plain
Discover more medicines within C10AX

Authorization and marketing

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

Country Identification scheme Identifier(s)
EE Ravimiamet 1795956, 1795967
FR Base de données publique des médicaments 65766872
GB Medicines & Healthcare Products Regulatory Agency 376465
IT Agenzia del Farmaco 047941012, 047941024
LT Valstybinė vaistų kontrolės tarnyba 1087707, 1087708
PL Rejestru Produktów Leczniczych 100421193
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W67657001, W67657002

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