Does ETOPOSIDE Cause Product use in unapproved indication? 2,774 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,774 reports of Product use in unapproved indication have been filed in association with ETOPOSIDE (Avopef). This represents 5.3% of all adverse event reports for ETOPOSIDE.
2,774
Reports of Product use in unapproved indication with ETOPOSIDE
5.3%
of all ETOPOSIDE reports
629
Deaths
648
Hospitalizations
How Dangerous Is Product use in unapproved indication From ETOPOSIDE?
Of the 2,774 reports, 629 (22.7%) resulted in death, 648 (23.4%) required hospitalization, and 266 (9.6%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETOPOSIDE. However, 2,774 reports have been filed with the FAERS database.
What Other Side Effects Does ETOPOSIDE Cause?
Off label use (6,495)
Febrile neutropenia (5,966)
Disease progression (3,776)
Drug ineffective (3,687)
Neutropenia (3,641)
Thrombocytopenia (3,085)
Anaemia (2,586)
Pyrexia (2,453)
Sepsis (2,211)
Pancytopenia (2,129)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which ETOPOSIDE Alternatives Have Lower Product use in unapproved indication Risk?
ETOPOSIDE vs ETORICOXIB
ETOPOSIDE vs ETRASIMOD ARGININE
ETOPOSIDE vs ETRAVIRINE
ETOPOSIDE vs EUCALYPTOL\MENTHOL\METHYL SALICYLATE\THYMOL
ETOPOSIDE vs EVEROLIMUS