TEYSUNO

This brand name is authorized in Austria, Cyprus, Estonia, Finland, Ireland, Lithuania, Netherlands, Poland, Romania, UK.

Active ingredients

The drug TEYSUNO contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII 1548R74NSZ - TEGAFUR
 

Tegafur is a prodrug of 5-FU with good oral bioavailability. Following oral administration, tegafur is gradually converted to 5-FU in vivo, mainly by CYP2A6 enzyme activity in the liver. 5-FU is metabolised by the liver enzyme DPD. 5-FU is activated within cells by phosphorylation to its active metabolite, 5-fluoro-deoxyuridine-monophosphate (FdUMP). FdUMP and reduced folate are bound to thymidylate synthase leading to formation of a ternary complex which inhibits DNA synthesis. In addition, 5-fluorouridine-triphosphate (FUTP) is incorporated into RNA causing disruption of RNA functions.

 
Read more about Tegafur
2
UNII UA8SE1325T - GIMERACIL
 
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3
UNII 5VT6420TIG - OTERACIL
 
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Medicine classification

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

ATC Group Classification
L01BC53 Tegafur, combinations L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01B Antimetabolites → L01BC Pyrimidine analogues
Discover more medicines within L01BC53

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 1523832, 1523843, 1523854, 1523865, 1598205
FI Lääkealan turvallisuus- ja kehittämiskeskus 134175, 185610, 482719, 582618
GB Medicines & Healthcare Products Regulatory Agency 203667, 203672
IE Health Products Regulatory Authority 88328, 88329
LT Valstybinė vaistų kontrolės tarnyba 1059833, 1059834, 1059835, 1059836, 1068424
NL Z-Index G-Standaard, PRK 102881, 102903
PL Rejestru Produktów Leczniczych 100353379, 100353391
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W58736001, W58736002, W58737001, W58737002

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