SEMUSTINE for Bone marrow conditioning regimen: Side Effects & Safety Data

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There are 96 adverse event reports in the FDA FAERS database where SEMUSTINE was used for Bone marrow conditioning regimen.

Most Reported Side Effects for SEMUSTINE

Side Effect	Reports	%	Deaths	Hosp.
Pneumonia	25	16.0%	7	4
Febrile neutropenia	21	13.5%	0	6
Product use in unapproved indication	16	10.3%	9	0
Cystitis haemorrhagic	14	9.0%	3	2
Drug ineffective	14	9.0%	4	2
Off label use	13	8.3%	5	2
Complications of bone marrow transplant	12	7.7%	9	0
Infection	12	7.7%	12	0
Post transplant lymphoproliferative disorder	12	7.7%	7	0
Pulmonary alveolar haemorrhage	12	7.7%	9	0
Gastrointestinal disorder	11	7.1%	0	0
Epstein-barr viraemia	10	6.4%	6	0
Haematotoxicity	9	5.8%	0	0
Cytomegalovirus infection	8	5.1%	3	2
Thrombocytopenia	8	5.1%	2	4