Does ALBUTEROL\BUDESONIDE Cause Product use issue? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Product use issue have been filed in association with ALBUTEROL\BUDESONIDE. This represents 6.1% of all adverse event reports for ALBUTEROL\BUDESONIDE.
43
Reports of Product use issue with ALBUTEROL\BUDESONIDE
6.1%
of all ALBUTEROL\BUDESONIDE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product use issue From ALBUTEROL\BUDESONIDE?
Of the 43 reports, 1 (2.3%) required hospitalization, and 1 (2.3%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBUTEROL\BUDESONIDE. However, 43 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which ALBUTEROL\BUDESONIDE Alternatives Have Lower Product 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