Does BUDESONIDE Cause Impaired quality of life? 229 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 229 reports of Impaired quality of life have been filed in association with BUDESONIDE (BREYNA). This represents 0.9% of all adverse event reports for BUDESONIDE.
229
Reports of Impaired quality of life with BUDESONIDE
0.9%
of all BUDESONIDE reports
0
Deaths
47
Hospitalizations
How Dangerous Is Impaired quality of life From BUDESONIDE?
Of the 229 reports, 47 (20.5%) required hospitalization, and 2 (0.9%) were considered life-threatening.
Is Impaired quality of life Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 229 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 Impaired quality of life?
DUPILUMAB (3,945)
DOCETAXEL (3,714)
ADALIMUMAB (725)
OXYCODONE (468)
INFLIXIMAB (447)
PREDNISONE (430)
VEDOLIZUMAB (372)
METHOTREXATE (279)
MESALAMINE (264)
ACETAMINOPHEN\OXYCODONE (203)
Which BUDESONIDE Alternatives Have Lower Impaired quality of life Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE