Does BUDESONIDE Cause Intentional product misuse? 826 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 826 reports of Intentional product misuse have been filed in association with BUDESONIDE (BREYNA). This represents 3.3% of all adverse event reports for BUDESONIDE.
826
Reports of Intentional product misuse with BUDESONIDE
3.3%
of all BUDESONIDE reports
33
Deaths
132
Hospitalizations
How Dangerous Is Intentional product misuse From BUDESONIDE?
Of the 826 reports, 33 (4.0%) resulted in death, 132 (16.0%) required hospitalization, and 35 (4.2%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 826 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 product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which BUDESONIDE Alternatives Have Lower Intentional product misuse Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE