Does AZATHIOPRINE Cause Wrong technique in product usage process? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Wrong technique in product usage process have been filed in association with AZATHIOPRINE (AZATHIOPRINE). This represents 0.1% of all adverse event reports for AZATHIOPRINE.
23
Reports of Wrong technique in product usage process with AZATHIOPRINE
0.1%
of all AZATHIOPRINE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Wrong technique in product usage process From AZATHIOPRINE?
Of the 23 reports, 4 (17.4%) required hospitalization, and 2 (8.7%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZATHIOPRINE. However, 23 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which AZATHIOPRINE Alternatives Have Lower Wrong technique in product usage process Risk?
AZATHIOPRINE vs AZD-1222
AZATHIOPRINE vs AZELAIC ACID
AZATHIOPRINE vs AZELASTINE
AZATHIOPRINE vs AZELASTINE\FLUTICASONE
AZATHIOPRINE vs AZELNIDIPINE