Does AZATHIOPRINE Cause Decreased activity? 33 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of Decreased activity have been filed in association with AZATHIOPRINE (AZATHIOPRINE). This represents 0.1% of all adverse event reports for AZATHIOPRINE.
33
Reports of Decreased activity with AZATHIOPRINE
0.1%
of all AZATHIOPRINE reports
0
Deaths
15
Hospitalizations
How Dangerous Is Decreased activity From AZATHIOPRINE?
Of the 33 reports, 15 (45.5%) required hospitalization, and 2 (6.1%) were considered life-threatening.
Is Decreased activity Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZATHIOPRINE. However, 33 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 Decreased activity?
NIRAPARIB (586)
SACUBITRIL\VALSARTAN (570)
RUXOLITINIB (558)
DUPILUMAB (231)
LEVOTHYROXINE (201)
TREPROSTINIL (195)
PREDNISONE (193)
ALBUTEROL (190)
EMTRICITABINE\TENOFOVIR DISOPROXIL (186)
TERIPARATIDE (156)
Which AZATHIOPRINE Alternatives Have Lower Decreased activity Risk?
AZATHIOPRINE vs AZD-1222
AZATHIOPRINE vs AZELAIC ACID
AZATHIOPRINE vs AZELASTINE
AZATHIOPRINE vs AZELASTINE\FLUTICASONE
AZATHIOPRINE vs AZELNIDIPINE