Wondering if anybody has had to transition from subcutaneous Actemra to intravenous Actemra? I’m currently on weekly subcutaneous while tapering prednisone, (down to 10 mg) and will soon need to get IV infusions because of changes to insurance.
Were the side effects more pronounced with the IV? And how do you feel being “tethered” to the infusion center monthly?
Thank you everyone in the PMRGCA network for your support over the years!