Susoctocog alfa
Medication
- US DailyMed: Obizur
category
- AU: B2[1]
- B02BD14 (WHO)
- AU: S4 (Prescription only)[2]
- CA: ℞-only[3]
- UK: POM (Prescription only)[4]
- US: ℞-only[5]
- EU: Rx-only[6]
- In general: ℞ (Prescription only)
- 1339940-90-7
- DB11606
- 6892UQT2GK
- D10831
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.[6][5][7]
Susoctocog alfa was approved for medical use in the United States in October 2014,[8][9] and for medical use in the European Union in November 2015.[6]
Factor VIII is one of the proteins needed for normal clotting of the blood.[6]
References
- ^ "Antihemophilic factor Use During Pregnancy". Drugs.com. 20 January 2020. Archived from the original on 16 July 2020. Retrieved 6 March 2020.
- ^ "Prescription medicines: registration of new chemical entities in Australia, 2016". Therapeutic Goods Administration (TGA). 21 June 2022. Archived from the original on 10 April 2023. Retrieved 10 April 2023.
- ^ "Health Canada New Drug Authorizations: 2015 Highlights". Health Canada. 4 May 2016. Archived from the original on 20 February 2020. Retrieved 7 April 2024.
- ^ "Obizur 500 U powder and solvent for solution for injection - Summary of Product Characteristics (SmPC)". (emc). 13 April 2017. Retrieved 3 September 2020.
- ^ a b "Obizur (antihemophilic factor- recombinant, porcine sequence kit". DailyMed. 2 January 2020. Archived from the original on 24 July 2021. Retrieved 6 March 2020.
- ^ a b c d "Obizur EPAR". European Medicines Agency. 6 March 2020. Archived from the original on 11 August 2020. Retrieved 6 March 2020.
- ^ Burness CB, Scott LJ (May 2016). "Susoctocog Alfa: A Review in Acquired Haemophilia A". Drugs. 76 (7): 815–21. doi:10.1007/s40265-016-0576-1. PMID 27098420. S2CID 10880049.
- ^ "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. Archived from the original on 17 December 2019. Retrieved 6 March 2020.
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Antihemorrhagics (B02)
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