Does AZACITIDINE Cause Product quality issue? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product quality issue have been filed in association with AZACITIDINE (Azacitidine). This represents 0.1% of all adverse event reports for AZACITIDINE.
12
Reports of Product quality issue with AZACITIDINE
0.1%
of all AZACITIDINE reports
4
Deaths
2
Hospitalizations
How Dangerous Is Product quality issue From AZACITIDINE?
Of the 12 reports, 4 (33.3%) resulted in death, 2 (16.7%) required hospitalization, and 1 (8.3%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZACITIDINE. However, 12 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 Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which AZACITIDINE Alternatives Have Lower Product quality issue Risk?
AZACITIDINE vs AZATHIOPRINE
AZACITIDINE vs AZD-1222
AZACITIDINE vs AZELAIC ACID
AZACITIDINE vs AZELASTINE
AZACITIDINE vs AZELASTINE\FLUTICASONE