TEYSUNO

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

Active ingredients

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

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

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