Does AZATHIOPRINE Cause Hepatic function abnormal? 352 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 352 reports of Hepatic function abnormal have been filed in association with AZATHIOPRINE (AZATHIOPRINE). This represents 1.1% of all adverse event reports for AZATHIOPRINE.
352
Reports of Hepatic function abnormal with AZATHIOPRINE
1.1%
of all AZATHIOPRINE reports
10
Deaths
69
Hospitalizations
How Dangerous Is Hepatic function abnormal From AZATHIOPRINE?
Of the 352 reports, 10 (2.8%) resulted in death, 69 (19.6%) required hospitalization, and 16 (4.5%) were considered life-threatening.
Is Hepatic function abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZATHIOPRINE. However, 352 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 Hepatic function abnormal?
NIVOLUMAB (1,131)
PEMBROLIZUMAB (1,079)
METHOTREXATE (1,054)
CABOZANTINIB S-MALATE (912)
CYCLOPHOSPHAMIDE (824)
BEVACIZUMAB (769)
PACLITAXEL (603)
LENVATINIB (528)
ATORVASTATIN (520)
CYCLOSPORINE (508)
Which AZATHIOPRINE Alternatives Have Lower Hepatic function abnormal Risk?
AZATHIOPRINE vs AZD-1222
AZATHIOPRINE vs AZELAIC ACID
AZATHIOPRINE vs AZELASTINE
AZATHIOPRINE vs AZELASTINE\FLUTICASONE
AZATHIOPRINE vs AZELNIDIPINE