Immune Globulin, Intramuscular

Table of contents

  • Brand Names
  • Pharmacologic Category
  • Mechanism of Action
  • Therapeutic Use
  • Pregnancy and Lactation Implications
  • Contraindications
  • Warnings and Precautions
  • Adverse Reactions
  • Genes that may be involved
  • Drug Interactions
  • Dosage
  • Pharmacokinetics and Pharmacodynamics
  • Special Considerations

Brand Names

Europe

Austria: Beriglobin P, Gammanorm, Subcuvia, Vibaglobin; Belgium: Subcuvia, Vivaglobin; Bulgaria: Human Normal Immunoglobulin; Cyprus: Subcuvia, Subgam; Czech Republic: Gammanorm, Igamplia, Pasteurised Human Immunoglobulin, Subcuvia, Vivaglobin; Denmark: Beriglobin, Gammanorm, Subcuvia, Vivaglobin; Estonia: Gammanorm, Subcuvia; Finland: Gammanorm, Subcuvia, Vivaglobin; France: Gammanorm, Subcuvia, Vivaglobin; Germany: Beriglobin, Gammanorm, Subcuvia, Vivaglobin; Greece: Subcuvia, Vivaglobin; Hungary: Gammanorm, Subcuvia; Ireland: Rophylac, Subcuvia; Italy: Subcuvia, Vivaglobin; Latvia: Subcuvia; Lithuania: Subcuvia; Netherlands: Gammanorm, GammaQuin; Poland: Bioglobulin, Gammanorm, Subcuvia, Vivaglobin; Portugal: Gammanorm, Subcuvia, Vivaglobin; Romania: Beriglobin; Slovakia: Gammanorm, Igamplia, Vivaglobin; Spain: Beriglobina P, Gammaglobulina Humana Pasteurizada, Vivaglobin; Sweden: Beriglobin, Gammanorm, Subcuvia, Vivaglobin; UK: Subgam, Vivaglobin.

North America

Canada: Gamastan, Immune Serum Globulin (Human), Vivaglobin; USA: Vivaglobin.

Latin America

Argentina: Igg Intramuscular; Brazil: Beriglobina, Imunoglobulin-Imunoglobulina Humana, Venimmuna; Mexico: Beriglobina P.

Drug combinations

Chemistry

Pharmacologic Category

Serums, Toxoids, and Vaccines; Serums. Immune Globulin. (ATC-Code: J06BA01).

Mechanism of action

Increases antibody titer and antigen-antibody reaction potential.

Therapeutic use

Provides passive immunity in susceptible individuals under the following circumstances: Hepatitis A, measles, varicella, rubella, tetanus, and immunoglobulin deficiency.

Pregnancy and lactiation implications

Immune globulins cross placenta in increased amounts after 30 weeks gestation. Reproduction studies not carried out.

Unlabeled use

Contraindications

Hypersensitivity to immune globulin or any component of the formulation. IgA deficiency. Severe thrombocytopenia or coagulation disorders where I.M. injections are contraindicated.

Warnings and precautions

Hypersensitivity and anaphylactic reactions can occur. Product of human plasma. Not for I.V. administration. Skin testing should be avoided (local irritation can occur).

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