Does BUDESONIDE Cause Device failure? 205 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 205 reports of Device failure have been filed in association with BUDESONIDE (BREYNA). This represents 0.8% of all adverse event reports for BUDESONIDE.
205
Reports of Device failure with BUDESONIDE
0.8%
of all BUDESONIDE reports
1
Deaths
10
Hospitalizations
How Dangerous Is Device failure From BUDESONIDE?
Of the 205 reports, 1 (0.5%) resulted in death, 10 (4.9%) required hospitalization, and 2 (1.0%) were considered life-threatening.
Is Device failure Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 205 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 failure?
EPINEPHRINE (1,344)
SOMATROPIN (1,141)
PEGFILGRASTIM (829)
TREPROSTINIL (713)
BACLOFEN (691)
BUDESONIDE\FORMOTEROL (686)
ETANERCEPT (576)
GOLIMUMAB (487)
LEVONORGESTREL (332)
ACLIDINIUM (304)
Which BUDESONIDE Alternatives Have Lower Device failure Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE