Immune Globulin Intramuscular (IGIM; IG; Gamma Globulin; ISG)

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Immune Globulin Intramuscular (IGIM; IG; Gamma Globulin; ISG)

  Action
  Indications
  Contraindications
  Route/Dosage
  Interactions
  Lab Test Interferences
  Adverse Reactions
  Precautions
Patient Care Considerations
  Administration/Storage
  Assessment/Interventions
  Patient/Family Education


(ih-MYOON GLAH-byoo-lin intramuscular)
BayGam
Class: Immune serum

 Action Replaces normal human IgG antibodies.

 Indications Passive immunization against or modification of hepatitis A. Prevention or modification of measles in susceptible persons exposed < 6 days previously. Passive immunization against varicella in immunocompromised patients if varicellazoster immune globulin (VZIG) is not available and IGIM can be given promptly. IgG replacement therapy in certain persons with hypoglobulinemia or agammaglobulinemia.

 Contraindications Immediate hypersensitivity to human antibody product or thimerosal; circulating anti-IgA antibodies; thrombocytopenia or any coagulation disorder.

 Route/Dosage

Preexposure and Postexposure Hepatitis A Prophylaxis

ADULTS & CHILDREN: IM 0.02 ml/kg. Pre-exposure hepatitis A prophylaxis for travelers to developing countries who will stay < 3 mo. IM 0.06 mg/kg with booster doses q 4–6 mo throughout their stay.

Postexposure Measles Prophylaxis

ADULTS & CHILDREN: IM 0.25 ml/kg. SUSCEPTIBLE IMMUNOCOMPROMISED CHILDREN: IM 0.5 ml/kg (max 15 ml).

Postexposure Varicella Prophylaxis

ADULTS & CHILDREN: If VZIG is unavailable, IM 0.6 to 1.2 ml/kg.

Immunoglobulin Deficiency

ADULTS & CHILDREN: IM 0.66 ml/kg (100 mg/kg) q 3 to 4 wk. Larger initial dose (eg, 1.2 ml/kg) is often given at onset of therapy. Patients who rapidly metabolize may require more frequent or larger doses.

 Interactions Live vaccines: To avoid inactivating vaccines containing live viruses or bacteria, give live vaccines 2 to 4 wk before or 3 to 6 mo after IGIU, depending on dose.

 Lab Test Interferences None well documented.

 Adverse Reactions

OTHER: Local pain and tenderness at injection site; urticaria; angioedema; anaphylactic reactions.

 Precautions

Pregnancy: Category C. Lactation: Undetermined. Special risk patients: Give drug cautiously to persons receiving anticoagulant therapy because of IM administration. Hypersensitivity: Hypersensitivity, including anaphylaxis, may occur. Administer drug with caution in patients with prior systemic allergic reactions to human immunoglobulins.


PATIENT CARE CONSIDERATIONS


 Administration/Storage

 Assessment/Interventions

 Patient/Family Education

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Copyright
© 2003 Facts and Comparisons
David S. Tatro
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