Does AZATHIOPRINE Cause Adverse event? 391 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 391 reports of Adverse event have been filed in association with AZATHIOPRINE (AZATHIOPRINE). This represents 1.2% of all adverse event reports for AZATHIOPRINE.
391
Reports of Adverse event with AZATHIOPRINE
1.2%
of all AZATHIOPRINE reports
136
Deaths
260
Hospitalizations
How Dangerous Is Adverse event From AZATHIOPRINE?
Of the 391 reports, 136 (34.8%) resulted in death, 260 (66.5%) required hospitalization, and 118 (30.2%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZATHIOPRINE. However, 391 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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which AZATHIOPRINE Alternatives Have Lower Adverse event Risk?
AZATHIOPRINE vs AZD-1222
AZATHIOPRINE vs AZELAIC ACID
AZATHIOPRINE vs AZELASTINE
AZATHIOPRINE vs AZELASTINE\FLUTICASONE
AZATHIOPRINE vs AZELNIDIPINE