Does AZACITIDINE Cause Product reconstitution quality issue? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Product reconstitution quality issue have been filed in association with AZACITIDINE (Azacitidine). This represents 0.1% of all adverse event reports for AZACITIDINE.
17
Reports of Product reconstitution quality issue with AZACITIDINE
0.1%
of all AZACITIDINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product reconstitution quality issue From AZACITIDINE?
Of the 17 reports.
Is Product reconstitution quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZACITIDINE. However, 17 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 reconstitution quality issue?
SOMATROPIN (149)
LEUPROLIDE (108)
RISPERIDONE (34)
TRIPTORELIN (28)
SULFUR HEXAFLUORIDE (23)
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (20)
HUMAN C1-ESTERASE INHIBITOR (20)
ONABOTULINUMTOXINA (16)
NALTREXONE (15)
TEDUGLUTIDE (15)
Which AZACITIDINE Alternatives Have Lower Product reconstitution quality issue Risk?
AZACITIDINE vs AZATHIOPRINE
AZACITIDINE vs AZD-1222
AZACITIDINE vs AZELAIC ACID
AZACITIDINE vs AZELASTINE
AZACITIDINE vs AZELASTINE\FLUTICASONE