3.1
D-Gam (Bio Products Laboratory) is extracted by fractionation and is suitable for intramuscular use only. It is sold as a solution ready for injection, and is available in vials containing 250, 500, 1,500 or 2,500 IU. The 500 IU dose has UK marketing authorisation for RAADP at 28 and 34 weeks gestation in non-sensitised women who are RhD negative, for use after potentially sensitising events that occur after 20 weeks gestation, and for use after the birth of an RhD-positive baby. The 250 IU dose has UK marketing authorisation for use after potentially sensitising events up to 20 weeks gestation, and the 1,500 and 2,500 IU doses have UK marketing authorisation for the treatment of large FMHs. D-Gam also has UK marketing authorisation for the treatment of people who are RhD negative and who have had transfusions of RhD-positive blood or blood products.