Does BUDESONIDE Cause Device use issue? 245 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 245 reports of Device use issue have been filed in association with BUDESONIDE (BREYNA). This represents 1.0% of all adverse event reports for BUDESONIDE.
245
Reports of Device use issue with BUDESONIDE
1.0%
of all BUDESONIDE reports
1
Deaths
18
Hospitalizations
How Dangerous Is Device use issue From BUDESONIDE?
Of the 245 reports, 1 (0.4%) resulted in death, 18 (7.3%) required hospitalization, and 4 (1.6%) were considered life-threatening.
Is Device use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 245 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 Device use issue?
SOMATROPIN (2,571)
LEVONORGESTREL (2,489)
COPPER (1,318)
BUDESONIDE\FORMOTEROL (1,236)
EXENATIDE (992)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (976)
DUPILUMAB (528)
ALIROCUMAB (471)
INSULIN GLARGINE (469)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (459)
Which BUDESONIDE Alternatives Have Lower Device use issue Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE