Does AZATHIOPRINE Cause Performance status decreased? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Performance status decreased have been filed in association with AZATHIOPRINE (AZATHIOPRINE). This represents 0.0% of all adverse event reports for AZATHIOPRINE.
7
Reports of Performance status decreased with AZATHIOPRINE
0.0%
of all AZATHIOPRINE reports
1
Deaths
5
Hospitalizations
How Dangerous Is Performance status decreased From AZATHIOPRINE?
Of the 7 reports, 1 (14.3%) resulted in death, 5 (71.4%) required hospitalization, and 1 (14.3%) were considered life-threatening.
Is Performance status decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZATHIOPRINE. However, 7 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 Performance status decreased?
BACLOFEN (156)
LENALIDOMIDE (118)
PACLITAXEL (112)
BEVACIZUMAB (103)
SODIUM OXYBATE (103)
CARBOPLATIN (100)
DEXAMETHASONE (80)
CAPECITABINE (75)
NIRAPARIB (75)
LUMATEPERONE (68)
Which AZATHIOPRINE Alternatives Have Lower Performance status decreased Risk?
AZATHIOPRINE vs AZD-1222
AZATHIOPRINE vs AZELAIC ACID
AZATHIOPRINE vs AZELASTINE
AZATHIOPRINE vs AZELASTINE\FLUTICASONE
AZATHIOPRINE vs AZELNIDIPINE