Susoctocog alfa
Susoctocog alfa, sold under the brand name Obizur, is a medication used for the treatment of bleeding episodes in adults with acquired haemophilia, a bleeding disorder caused by the spontaneous development of antibodies that inactivate factor VIII.[2][3]
Clinical data | |
---|---|
Trade names | Obizur |
Other names | Antihemophilic factor (recombinant) |
AHFS/Drugs.com | Monograph |
License data | |
Pregnancy category | |
Drug class | Antihemophilic factor |
ATC code | |
Legal status | |
Legal status |
|
Identifiers | |
DrugBank | |
UNII |
Susoctocog alfa was approved for medical use in the United States in October 2014,[4][5] and for medical use in the European Union in November 2015.[2]
Factor VIII is one of the proteins needed for normal clotting of the blood.[2]
References
- "Antihemophilic factor Use During Pregnancy". Drugs.com. 20 January 2020. Retrieved 6 March 2020.
- "Obizur EPAR". European Medicines Agency. 6 March 2020. Retrieved 6 March 2020.
- "Obizur (antihemophilic factor- recombinant, porcine sequence kit". DailyMed. 2 January 2020. Retrieved 6 March 2020.
- "Obizur". U.S. Food and Drug Administration (FDA). 13 March 2018. Archived from the original on 23 April 2019. Retrieved 6 March 2020.
- "Obizur". U.S. Food and Drug Administration (FDA). 27 September 2019. STN: BL 125512. Retrieved 6 March 2020.
External links
- "Susoctocog alfa". Drug Information Portal. U.S. National Library of Medicine.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.