Does AZATHIOPRINE Cause Incorrect product administration duration? 71 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 71 reports of Incorrect product administration duration have been filed in association with AZATHIOPRINE (AZATHIOPRINE). This represents 0.2% of all adverse event reports for AZATHIOPRINE.
71
Reports of Incorrect product administration duration with AZATHIOPRINE
0.2%
of all AZATHIOPRINE reports
64
Deaths
66
Hospitalizations
How Dangerous Is Incorrect product administration duration From AZATHIOPRINE?
Of the 71 reports, 64 (90.1%) resulted in death, 66 (93.0%) required hospitalization, and 63 (88.7%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZATHIOPRINE. However, 71 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which AZATHIOPRINE Alternatives Have Lower Incorrect product administration duration Risk?
AZATHIOPRINE vs AZD-1222
AZATHIOPRINE vs AZELAIC ACID
AZATHIOPRINE vs AZELASTINE
AZATHIOPRINE vs AZELASTINE\FLUTICASONE
AZATHIOPRINE vs AZELNIDIPINE