Does ALBUTEROL\BUDESONIDE Cause Device malfunction? 71 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 71 reports of Device malfunction have been filed in association with ALBUTEROL\BUDESONIDE. This represents 10.0% of all adverse event reports for ALBUTEROL\BUDESONIDE.
71
Reports of Device malfunction with ALBUTEROL\BUDESONIDE
10.0%
of all ALBUTEROL\BUDESONIDE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device malfunction From ALBUTEROL\BUDESONIDE?
Of the 71 reports.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBUTEROL\BUDESONIDE. However, 71 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)
Incorrect dose administered by device (69)
Asthma (67)
Incorrect dose administered (64)
Dyspnoea (63)
Drug ineffective (62)
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 ALBUTEROL\BUDESONIDE Alternatives Have Lower Device malfunction Risk?
ALBUTEROL\BUDESONIDE vs ALBUTEROL\IPRATROPIUM
ALBUTEROL\BUDESONIDE vs ALCAFTADINE
ALBUTEROL\BUDESONIDE vs ALCOHOL
ALBUTEROL\BUDESONIDE vs ALCOHOL\CHLORHEXIDINE
ALBUTEROL\BUDESONIDE vs ALDACTONE