Does BUDESONIDE Cause Device malfunction? 583 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 583 reports of Device malfunction have been filed in association with BUDESONIDE (BREYNA). This represents 2.3% of all adverse event reports for BUDESONIDE.
583
Reports of Device malfunction with BUDESONIDE
2.3%
of all BUDESONIDE reports
1
Deaths
44
Hospitalizations
How Dangerous Is Device malfunction From BUDESONIDE?
Of the 583 reports, 1 (0.2%) resulted in death, 44 (7.5%) required hospitalization, and 6 (1.0%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 583 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 malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
Which BUDESONIDE Alternatives Have Lower Device malfunction Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE