Does AZATHIOPRINE Cause Product use issue? 1,165 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,165 reports of Product use issue have been filed in association with AZATHIOPRINE (AZATHIOPRINE). This represents 3.5% of all adverse event reports for AZATHIOPRINE.
1,165
Reports of Product use issue with AZATHIOPRINE
3.5%
of all AZATHIOPRINE reports
430
Deaths
671
Hospitalizations
How Dangerous Is Product use issue From AZATHIOPRINE?
Of the 1,165 reports, 430 (36.9%) resulted in death, 671 (57.6%) required hospitalization, and 385 (33.0%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZATHIOPRINE. However, 1,165 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which AZATHIOPRINE Alternatives Have Lower Product use issue Risk?
AZATHIOPRINE vs AZD-1222
AZATHIOPRINE vs AZELAIC ACID
AZATHIOPRINE vs AZELASTINE
AZATHIOPRINE vs AZELASTINE\FLUTICASONE
AZATHIOPRINE vs AZELNIDIPINE