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Adverse event reporting can be found at the bottom of the page

Administration and Storage Choosing ReFacto AFChoosing ReFacto AFChoosing ReFacto AFPersonalised dosing 

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Product InformationProduct InformationLaboratory StandardEfficacy & SafetyAdministration & StorageSupport & ResourcesSupport & ResourcesMaterialsVideosOrdering ReFacto AFContact Us

For ReFacto AF® (moroctocog alfa) Prescribing Information for Great Britain and Northern Ireland click here.
Adverse event reporting information can be found at the bottom of the page.

Administration & StorageAdministration

ReFacto AF® can be reconstituted and administered using our R2 or FuseNGo devices.

Administration: intravenous infusion1

  • Administered by intravenous infusion over several minutes after reconstitution of the lyophilised powder for injection with sodium chloride 9 mg/mL (0.9%) solution for injection (provided).The rate of administration should be determined by the patient's comfort level.1
  • ReFacto AF can be administered with two types of devices: R2 reconstitution device (powder and solvent for solution for injection)2, and FuseNGo all in one reconstitution device (powder and solvent for solution for injection in pre-filled syringe).3
  • For further support, refer to the Refacto AF Infusion mat step-by-step guide. Download the R2 and FuseNGo Infusion mats here. 
Request printed copies or other materials through our Contact Us page.
Storage

How to store ReFacto AF®:

  • Store and transport refrigerated (2°C - 8°C).1
  • Do not freeze.1
  • Keep the product in the outer carton to protect it from light.1
  • ReFacto AF® has a shelf life of 3 years.1
  • The product may be removed from refrigerated storage for one single period of maximum 3 months at room temperature (up to 25°C).1
  • At the end of this period of room temperature storage, the product must not be returned to refrigerated storage, but is to be used or discarded.1

After reconstitution:
  • Chemical and physical in-use stability has been demonstrated for 3 hours at temperatures up to 25°C.1
  • The product does not contain a preservative.1
  • The reconstituted product should be used immediately, or within 3 hours after reconstitution.1
Explore MorePersonalised Dosing

Access information to help determine adequate dosing for your patient and improve their peak control.

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Materials

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Contact Us

Contact us for more information on ReFacto AF and download our FAQ for supply and stock related queries.

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References

ReFacto AF® Summary of Product Characteristics. For Great Britain, available here. For Northern Ireland, available here.ReFacto AF® powder and solvent for solution for injection Patient Information LeafletReFacto AF® powder and solvent for solution for injection in pre-filled syringe Patient Information Leaflet
PP-REF-GBR-0352. July 2023

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search 

for MHRA Yellow Card in Google Play or Apple App Store

 

Adverse events should also be reported to Pfizer Medical Information on 01304 616161

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