Immunology

Aim to use the dose that achieves a significant reduction in the number of infections. SCIG and IVIG are equally effective. Continued use of IG should be based on objective measures of effectiveness established at the outset of treatment. These measures should be assessed no later than 6 months after initiation of treatment and at least annually thereafter by a physician with recognized expertise in immunodeficiency disorders.

Hematopoietic Stem Cell Transplant in primary immunodeficiencies

Recommended Indications in which IG can be used

Order Number: I3-HSCTPID

Hypogammaglobulinemia, secondary immunodeficiency disorders (SID)

Recommended Indications in which IG can be used

Order Number: I2-SID

Primary immunodeficiency (PID) disorders

Recommended Indications in which IG can be used

Order Number: I1-PID