Update on Recall of Bayer Kogenate FS from National Organizations
Patient organizations are in ongoing communication with manufacturer
Update on Recall of Bayer Kogenate FS from National Organizations Read More »
Patient organizations are in ongoing communication with manufacturer
Update on Recall of Bayer Kogenate FS from National Organizations Read More »
Last week, Bayer announced the recall of two lots of Kogenate® FS antihemophilic factor (recombinant) 2000 IU vials. That highly concerning announcement has raised many questions on the part of both national organizations and community members.
National Joint Statement on Recall of Bayer Kogenate FS Lots Read More »
July 19, 2019 Bayer has announced a recall of two lots of Kogenate® FS 2000 IU vials.
Medical Advisory: Bayer Announces Recall of Two Lots of Kogenate FS Read More »
If you are currently using Monoclate-P®, please contact your physician or hemophilia treatment center to learn about other options that are available to you for treatment.
CSL Behring Discontinues Production and Distribution of Monoclate-P® Read More »
If you have questions or concerns, please reach out to Genentech and/or your physician.
Genentech Issues Statement on Hemlibra Read More »
The Company has suspended dosing in all ongoing fitusiran studies pending further review of the safety event and development of a risk mitigation strategy.
Alnylam Suspends Fitusiran Dosing due to Thrombotic Event Read More »