Does THIOTEPA Cause Device related bacteraemia? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Device related bacteraemia have been filed in association with THIOTEPA (Thiotepa). This represents 0.2% of all adverse event reports for THIOTEPA.
11
Reports of Device related bacteraemia with THIOTEPA
0.2%
of all THIOTEPA reports
11
Deaths
0
Hospitalizations
How Dangerous Is Device related bacteraemia From THIOTEPA?
Of the 11 reports, 11 (100.0%) resulted in death.
Is Device related bacteraemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for THIOTEPA. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does THIOTEPA Cause?
Off label use (762)
Febrile neutropenia (645)
Mucosal inflammation (616)
Cytomegalovirus infection (446)
Product use in unapproved indication (425)
Pyrexia (359)
Drug ineffective (358)
Acute graft versus host disease in skin (355)
Acute graft versus host disease (331)
Cytomegalovirus infection reactivation (325)
What Other Drugs Cause Device related bacteraemia?
TEDUGLUTIDE (40)
CYCLOPHOSPHAMIDE (29)
PREDNISONE (23)
CYTARABINE (21)
MYCOPHENOLATE MOFETIL (20)
TACROLIMUS (20)
METHOTREXATE (19)
RITUXIMAB (19)
DINUTUXIMAB BETA (17)
ISOTRETINOIN (17)
Which THIOTEPA Alternatives Have Lower Device related bacteraemia Risk?
THIOTEPA vs THIOTHIXENE
THIOTEPA vs THROMBIN
THIOTEPA vs THROMBIN HUMAN
THIOTEPA vs THYMOCYTE IMMUNE GLOBULIN NOS
THIOTEPA vs THYMOGLOBULINE