Does TOPOTECAN Cause Product use issue? 108 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 108 reports of Product use issue have been filed in association with TOPOTECAN (HYCAMTIN). This represents 3.1% of all adverse event reports for TOPOTECAN.
108
Reports of Product use issue with TOPOTECAN
3.1%
of all TOPOTECAN reports
10
Deaths
27
Hospitalizations
How Dangerous Is Product use issue From TOPOTECAN?
Of the 108 reports, 10 (9.3%) resulted in death, 27 (25.0%) required hospitalization, and 4 (3.7%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOPOTECAN. However, 108 reports have been filed with the FAERS database.
What Other Side Effects Does TOPOTECAN Cause?
Febrile neutropenia (425)
Off label use (390)
Death (332)
Product use in unapproved indication (323)
Neutropenia (255)
Pyrexia (252)
Anaemia (242)
Malignant neoplasm progression (238)
Drug ineffective (216)
Disease progression (207)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which TOPOTECAN Alternatives Have Lower Product use issue Risk?
TOPOTECAN vs TOPOTECAN\TOPOTECAN
TOPOTECAN vs TOPROL
TOPOTECAN vs TOREMIFENE
TOPOTECAN vs TORIPALIMAB
TOPOTECAN vs TORSEMIDE