Does AZATHIOPRINE Cause Product quality issue? 293 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 293 reports of Product quality issue have been filed in association with AZATHIOPRINE (AZATHIOPRINE). This represents 0.9% of all adverse event reports for AZATHIOPRINE.
293
Reports of Product quality issue with AZATHIOPRINE
0.9%
of all AZATHIOPRINE reports
288
Deaths
242
Hospitalizations
How Dangerous Is Product quality issue From AZATHIOPRINE?
Of the 293 reports, 288 (98.3%) resulted in death, 242 (82.6%) required hospitalization, and 243 (82.9%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZATHIOPRINE. However, 293 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which AZATHIOPRINE Alternatives Have Lower Product quality issue Risk?
AZATHIOPRINE vs AZD-1222
AZATHIOPRINE vs AZELAIC ACID
AZATHIOPRINE vs AZELASTINE
AZATHIOPRINE vs AZELASTINE\FLUTICASONE
AZATHIOPRINE vs AZELNIDIPINE