Does ALBUTEROL\BUDESONIDE Cause Device defective? 47 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 47 reports of Device defective have been filed in association with ALBUTEROL\BUDESONIDE. This represents 6.6% of all adverse event reports for ALBUTEROL\BUDESONIDE.
47
Reports of Device defective with ALBUTEROL\BUDESONIDE
6.6%
of all ALBUTEROL\BUDESONIDE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device defective From ALBUTEROL\BUDESONIDE?
Of the 47 reports.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBUTEROL\BUDESONIDE. However, 47 reports have been filed with the FAERS database.
What Other Side Effects Does ALBUTEROL\BUDESONIDE Cause?
Device delivery system issue (244)
Wrong technique in device usage process (110)
Product dose omission issue (109)
Device use issue (83)
Wrong technique in product usage process (82)
Device malfunction (71)
Incorrect dose administered by device (69)
Asthma (67)
Incorrect dose administered (64)
Dyspnoea (63)
What Other Drugs Cause Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
Which ALBUTEROL\BUDESONIDE Alternatives Have Lower Device defective Risk?
ALBUTEROL\BUDESONIDE vs ALBUTEROL\IPRATROPIUM
ALBUTEROL\BUDESONIDE vs ALCAFTADINE
ALBUTEROL\BUDESONIDE vs ALCOHOL
ALBUTEROL\BUDESONIDE vs ALCOHOL\CHLORHEXIDINE
ALBUTEROL\BUDESONIDE vs ALDACTONE