Does BUDESONIDE Cause Device delivery system issue? 150 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 150 reports of Device delivery system issue have been filed in association with BUDESONIDE (BREYNA). This represents 0.6% of all adverse event reports for BUDESONIDE.
150
Reports of Device delivery system issue with BUDESONIDE
0.6%
of all BUDESONIDE reports
0
Deaths
6
Hospitalizations
How Dangerous Is Device delivery system issue From BUDESONIDE?
Of the 150 reports, 6 (4.0%) required hospitalization, and 4 (2.7%) were considered life-threatening.
Is Device delivery system issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 150 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 delivery system issue?
ALBUTEROL (9,509)
SOMATROPIN (1,848)
EXENATIDE (1,533)
BUDESONIDE\FORMOTEROL (1,260)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (1,181)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (523)
LEVALBUTEROL (459)
MOMETASONE FUROATE\OLOPATADINE (347)
ABATACEPT (342)
PEGFILGRASTIM (323)
Which BUDESONIDE Alternatives Have Lower Device delivery system issue Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE