Does DECITABINE Cause Product use in unapproved indication? 195 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 195 reports of Product use in unapproved indication have been filed in association with DECITABINE (Decitabine). This represents 6.5% of all adverse event reports for DECITABINE.
195
Reports of Product use in unapproved indication with DECITABINE
6.5%
of all DECITABINE reports
59
Deaths
17
Hospitalizations
How Dangerous Is Product use in unapproved indication From DECITABINE?
Of the 195 reports, 59 (30.3%) resulted in death, 17 (8.7%) required hospitalization, and 3 (1.5%) 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 DECITABINE. However, 195 reports have been filed with the FAERS database.
What Other Side Effects Does DECITABINE Cause?
Febrile neutropenia (336)
Off label use (292)
Drug ineffective (253)
Pneumonia (243)
Myelosuppression (233)
Neutropenia (193)
Sepsis (175)
Acute myeloid leukaemia (172)
Thrombocytopenia (170)
Disease progression (156)
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 DECITABINE Alternatives Have Lower Product use in unapproved indication Risk?
DECITABINE vs DEFERASIROX
DECITABINE vs DEFERIPRONE
DECITABINE vs DEFEROXAMINE
DECITABINE vs DEFIBROTIDE
DECITABINE vs DEFLAZACORT