FDA Alert on CellCept (mycophenolate
mofetil) Causing Birth Defects and Miscarriage 5-16-08FDA
ALERT [5/16/2008] - Inosine Monophosphate Dehydrogenase Inhibitors (IMPDH)
Immunosuppressants
FDA is aware of reports of infants born with serious
congenital anomalies, including microtia and cleft lip and palate, following
exposure to mycophenolate mofetil (MMF) during pregnancy. MMF, the active drug
substance in CellCept, is an ester of the active metabolite mycophenolic acid
(MPA), the active drug substance in Myfortic. In most cases, the mothers were
taking MMF following an organ transplant to prevent organ rejection. However,
some mothers taking MMF were being treated for immune-mediated conditions such
as systemic lupus erythematosus (SLE) and erythema multiforme. Treatment began
before their pregnancies and continued into the first trimester or until the
pregnancy was detected. MMF is approved in the U.S. for use in the prophylaxis
of organ rejection in patients receiving allogeneic renal, cardiac or hepatic
transplants and MPA is approved in the U.S. for use in the prophylaxis of
organ rejection in patients receiving allogeneic renal transplants. In
patients who are
transplant recipients, these drugs are almost always used in
combination with other immunosuppressant drugs.
MMF and MPA increase the risk of spontaneous abortion in the first trimester
and can cause congenital malformations in the offspring of women who are
treated during pregnancy. The labeling for both MMF and MPA was revised in
November 2007 to change the Pregnancy Category to "D" (positive evidence of
human fetal risk, but potential benefits may warrant use of the drug in
pregnant women despite the potential risk) and to add these findings about the
risk of
early
pregnancy loss and congenital malformations to the boxed
warning.
FDA is continuing to work with the manufacturers of these drug products to
develop and implement means to mitigate the risks of
fetal exposure.
This
information reflects FDA's current analysis of data available to FDA
concerning this drug. FDA intends to update this when additional information
or analyses become available.
