Does BUDESONIDE Cause Condition aggravated? 1,548 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,548 reports of Condition aggravated have been filed in association with BUDESONIDE (BREYNA). This represents 6.2% of all adverse event reports for BUDESONIDE.
1,548
Reports of Condition aggravated with BUDESONIDE
6.2%
of all BUDESONIDE reports
131
Deaths
748
Hospitalizations
How Dangerous Is Condition aggravated From BUDESONIDE?
Of the 1,548 reports, 131 (8.5%) resulted in death, 748 (48.3%) required hospitalization, and 232 (15.0%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 1,548 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)
Fatigue (1,508)
Headache (1,501)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which BUDESONIDE Alternatives Have Lower Condition aggravated Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE