Does AZACITIDINE Cause Intentional product use issue? 80 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 80 reports of Intentional product use issue have been filed in association with AZACITIDINE (Azacitidine). This represents 0.4% of all adverse event reports for AZACITIDINE.
80
Reports of Intentional product use issue with AZACITIDINE
0.4%
of all AZACITIDINE reports
26
Deaths
34
Hospitalizations
How Dangerous Is Intentional product use issue From AZACITIDINE?
Of the 80 reports, 26 (32.5%) resulted in death, 34 (42.5%) required hospitalization, and 4 (5.0%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZACITIDINE. However, 80 reports have been filed with the FAERS database.
What Other Side Effects Does AZACITIDINE Cause?
Febrile neutropenia (2,172)
Death (1,853)
Pneumonia (1,315)
Neutropenia (1,176)
Acute myeloid leukaemia (1,156)
Off label use (1,064)
Pyrexia (1,011)
Thrombocytopenia (968)
Myelosuppression (952)
Anaemia (857)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which AZACITIDINE Alternatives Have Lower Intentional product use issue Risk?
AZACITIDINE vs AZATHIOPRINE
AZACITIDINE vs AZD-1222
AZACITIDINE vs AZELAIC ACID
AZACITIDINE vs AZELASTINE
AZACITIDINE vs AZELASTINE\FLUTICASONE