Does BUDESONIDE Cause Device issue? 339 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 339 reports of Device issue have been filed in association with BUDESONIDE (BREYNA). This represents 1.4% of all adverse event reports for BUDESONIDE.
339
Reports of Device issue with BUDESONIDE
1.4%
of all BUDESONIDE reports
1
Deaths
33
Hospitalizations
How Dangerous Is Device issue From BUDESONIDE?
Of the 339 reports, 1 (0.3%) resulted in death, 33 (9.7%) required hospitalization, and 3 (0.9%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 339 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which BUDESONIDE Alternatives Have Lower Device issue Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE