Does ALBUTEROL\BUDESONIDE Cause Device use issue? 83 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 83 reports of Device use issue have been filed in association with ALBUTEROL\BUDESONIDE. This represents 11.7% of all adverse event reports for ALBUTEROL\BUDESONIDE.
83
Reports of Device use issue with ALBUTEROL\BUDESONIDE
11.7%
of all ALBUTEROL\BUDESONIDE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device use issue From ALBUTEROL\BUDESONIDE?
Of the 83 reports, 1 (1.2%) required hospitalization.
Is Device use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBUTEROL\BUDESONIDE. However, 83 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)
Wrong technique in product usage process (82)
Device malfunction (71)
Incorrect dose administered by device (69)
Asthma (67)
Incorrect dose administered (64)
Dyspnoea (63)
Drug ineffective (62)
What Other Drugs Cause Device use issue?
SOMATROPIN (2,571)
LEVONORGESTREL (2,489)
COPPER (1,318)
BUDESONIDE\FORMOTEROL (1,236)
EXENATIDE (992)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (976)
DUPILUMAB (528)
ALIROCUMAB (471)
INSULIN GLARGINE (469)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (459)
Which ALBUTEROL\BUDESONIDE Alternatives Have Lower Device use issue Risk?
ALBUTEROL\BUDESONIDE vs ALBUTEROL\IPRATROPIUM
ALBUTEROL\BUDESONIDE vs ALCAFTADINE
ALBUTEROL\BUDESONIDE vs ALCOHOL
ALBUTEROL\BUDESONIDE vs ALCOHOL\CHLORHEXIDINE
ALBUTEROL\BUDESONIDE vs ALDACTONE