Bivigam (igiv) Pregnancy Warnings
Use is not recommended unless clearly needed.
AU TGA pregnancy category: C
US FDA pregnancy category: C
Animal studies have not been performed. There are no controlled data in human pregnancy. Intact immune globulins cross the placenta increasingly after 30 weeks gestation. Clinical experience with immunoglobulins does not suggest a harmful effect on pregnancy or the fetus. When administered prior to delivery in mothers with immune thrombocytopenic purpura, the platelet response and clinical effect were similar in the mother and the neonate.
AU TGA pregnancy category C: Drugs which, owing to their pharmacological effects, have caused or may be suspected of causing, harmful effects on the human fetus or neonate without causing malformations. These effects may be reversible. Accompanying texts should be consulted for further details.
US FDA pregnancy category C: Animal reproduction studies have shown an adverse effect on the fetus and there are no adequate and well-controlled studies in humans, but potential benefits may warrant use of the drug in pregnant women despite potential risks.
See references