Does BUDESONIDE 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 BUDESONIDE (BREYNA). This represents 0.0% of all adverse event reports for BUDESONIDE.
7
Reports of Performance status decreased with BUDESONIDE
0.0%
of all BUDESONIDE reports
3
Deaths
2
Hospitalizations
How Dangerous Is Performance status decreased From BUDESONIDE?
Of the 7 reports, 3 (42.9%) resulted in death, 2 (28.6%) required hospitalization.
Is Performance status decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does BUDESONIDE Cause?
Asthma (4,544)
Dyspnoea (4,441)
Drug ineffective (4,384)
Off label use (3,033)
Wheezing (2,590)
Cough (2,269)
Therapeutic product effect incomplete (2,191)
Loss of personal independence in daily activities (1,890)
Condition aggravated (1,548)
Fatigue (1,508)
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 BUDESONIDE Alternatives Have Lower Performance status decreased Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE