Does BUDESONIDE Cause Intentional device misuse? 292 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 292 reports of Intentional device misuse have been filed in association with BUDESONIDE (BREYNA). This represents 1.2% of all adverse event reports for BUDESONIDE.
292
Reports of Intentional device misuse with BUDESONIDE
1.2%
of all BUDESONIDE reports
0
Deaths
24
Hospitalizations
How Dangerous Is Intentional device misuse From BUDESONIDE?
Of the 292 reports, 24 (8.2%) required hospitalization, and 3 (1.0%) were considered life-threatening.
Is Intentional device misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 292 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 Intentional device misuse?
BUDESONIDE\FORMOTEROL (1,318)
EXENATIDE (1,254)
ACLIDINIUM (346)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (182)
SOMATROPIN (128)
TERIPARATIDE (117)
FORMOTEROL\GLYCOPYRROLATE (103)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (102)
CARBIDOPA\LEVODOPA (100)
LEVONORGESTREL (82)
Which BUDESONIDE Alternatives Have Lower Intentional device misuse Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE