Does AZATHIOPRINE Cause Intentional product use issue? 948 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 948 reports of Intentional product use issue have been filed in association with AZATHIOPRINE (AZATHIOPRINE). This represents 2.9% of all adverse event reports for AZATHIOPRINE.
948
Reports of Intentional product use issue with AZATHIOPRINE
2.9%
of all AZATHIOPRINE reports
626
Deaths
596
Hospitalizations
How Dangerous Is Intentional product use issue From AZATHIOPRINE?
Of the 948 reports, 626 (66.0%) resulted in death, 596 (62.9%) required hospitalization, and 479 (50.5%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZATHIOPRINE. However, 948 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which AZATHIOPRINE Alternatives Have Lower Intentional product use issue Risk?
AZATHIOPRINE vs AZD-1222
AZATHIOPRINE vs AZELAIC ACID
AZATHIOPRINE vs AZELASTINE
AZATHIOPRINE vs AZELASTINE\FLUTICASONE
AZATHIOPRINE vs AZELNIDIPINE