Does AZATHIOPRINE Cause Full blood count abnormal? 241 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 241 reports of Full blood count abnormal have been filed in association with AZATHIOPRINE (AZATHIOPRINE). This represents 0.7% of all adverse event reports for AZATHIOPRINE.
241
Reports of Full blood count abnormal with AZATHIOPRINE
0.7%
of all AZATHIOPRINE reports
60
Deaths
110
Hospitalizations
How Dangerous Is Full blood count abnormal From AZATHIOPRINE?
Of the 241 reports, 60 (24.9%) resulted in death, 110 (45.6%) required hospitalization, and 148 (61.4%) were considered life-threatening.
Is Full blood count abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZATHIOPRINE. However, 241 reports have been filed with the FAERS database.
What Other Side Effects Does AZATHIOPRINE Cause?
Drug ineffective (8,076)
Off label use (5,358)
Drug intolerance (3,392)
Condition aggravated (2,832)
Rheumatoid arthritis (2,746)
Treatment failure (2,483)
Arthralgia (2,427)
Drug hypersensitivity (2,421)
Nausea (2,178)
Pneumonia (2,157)
What Other Drugs Cause Full blood count abnormal?
ALBUTEROL (3,060)
PREDNISONE (2,230)
BUDESONIDE\FORMOTEROL (1,786)
TIOTROPIUM (1,754)
MONTELUKAST (1,529)
MEPOLIZUMAB (1,440)
BUDESONIDE (1,339)
PALBOCICLIB (1,146)
CICLESONIDE (916)
PANTOPRAZOLE (776)
Which AZATHIOPRINE Alternatives Have Lower Full blood count abnormal Risk?
AZATHIOPRINE vs AZD-1222
AZATHIOPRINE vs AZELAIC ACID
AZATHIOPRINE vs AZELASTINE
AZATHIOPRINE vs AZELASTINE\FLUTICASONE
AZATHIOPRINE vs AZELNIDIPINE