ESPEROCT

This brand name is authorized in Austria, Estonia, Spain, Finland, Croatia, Ireland, Israel, Japan, Lithuania, Netherlands, Poland, Romania, Turkey, United Kingdom

Active ingredients

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

1 Coagulation factor VIII UNII 969NZA3X9T - TUROCTOCOG ALFA

Activated factor VIII acts as a cofactor for activated factor IX, accelerating the conversion of factor X to activated factor X (factor Xa). Haemophilia A is a sex-linked hereditary disorder of blood coagulation due to decreased levels of factor VIII:C. By replacement therapy the plasma levels of factor VIII are increased, thereby enabling a temporary correction of the factor deficiency and correction of the bleeding tendencies. Read about Coagulation factor VIII

Medicine classification

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

ATC code	Group title	Classification
B02BD02	Coagulation factor VIII	B Blood and blood forming organs → B02 Antihemorrhagics → B02B Vitamin K and other hemostatics → B02BD Blood coagulation factors
Discover more medicines within B02BD02

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): 1798566, 1798577, 1798599, 1798601, 1798612
Country: ES	Centro de información online de medicamentos de la AEMPS	Identifier(s): 1191374001, 1191374002, 1191374003, 1191374004, 1191374005
Country: FI	Lääkealan turvallisuus- ja kehittämiskeskus	Identifier(s): 122801, 424592, 488546, 520444, 588978
Country: GB	Medicines & Healthcare Products Regulatory Agency	Identifier(s): 384809, 384841, 384846, 384849, 384852
Country: IL	מִשְׂרַד הַבְּרִיאוּת	Identifier(s): 9208
Country: JP	医薬品医療機器総合機構	Identifier(s): 6343454D1025, 6343454D2021, 6343454D3028, 6343454D4024, 6343454D5020
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 1088090, 1088091, 1088092, 1088093, 1088094
Country: NL	Z-Index G-Standaard, PRK	Identifier(s): 199125, 199133, 199168, 199176, 199184
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100423246, 100423335, 100423341, 100423358, 100423364
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): W66807001, W66808001, W66809001, W66810001, W66811001
Country: TR	İlaç ve Tıbbi Cihaz Kurumu	Identifier(s): 8699676791187, 8699676791194, 8699676791200, 8699676791217, 8699676791224