Does THIOTEPA Cause Febrile neutropenia? 645 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 645 reports of Febrile neutropenia have been filed in association with THIOTEPA (Thiotepa). This represents 9.4% of all adverse event reports for THIOTEPA.
645
Reports of Febrile neutropenia with THIOTEPA
9.4%
of all THIOTEPA reports
89
Deaths
144
Hospitalizations
How Dangerous Is Febrile neutropenia From THIOTEPA?
Of the 645 reports, 89 (13.8%) resulted in death, 144 (22.3%) required hospitalization, and 68 (10.5%) were considered life-threatening.
Is Febrile neutropenia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for THIOTEPA. However, 645 reports have been filed with the FAERS database.
What Other Side Effects Does THIOTEPA Cause?
Off label use (762)
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)
Infection (318)
What Other Drugs Cause Febrile neutropenia?
CYCLOPHOSPHAMIDE (11,318)
DOXORUBICIN (8,844)
VINCRISTINE (8,676)
RITUXIMAB (6,382)
CYTARABINE (6,142)
METHOTREXATE (6,091)
ETOPOSIDE (5,966)
CARBOPLATIN (4,888)
DEXAMETHASONE (4,382)
PREDNISONE (3,956)
Which THIOTEPA Alternatives Have Lower Febrile neutropenia Risk?
THIOTEPA vs THIOTHIXENE
THIOTEPA vs THROMBIN
THIOTEPA vs THROMBIN HUMAN
THIOTEPA vs THYMOCYTE IMMUNE GLOBULIN NOS
THIOTEPA vs THYMOGLOBULINE