Does ALBUTEROL\BUDESONIDE Cause Device delivery system issue? 244 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 244 reports of Device delivery system issue have been filed in association with ALBUTEROL\BUDESONIDE. This represents 34.3% of all adverse event reports for ALBUTEROL\BUDESONIDE.
244
Reports of Device delivery system issue with ALBUTEROL\BUDESONIDE
34.3%
of all ALBUTEROL\BUDESONIDE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device delivery system issue From ALBUTEROL\BUDESONIDE?
Of the 244 reports, 1 (0.4%) required hospitalization.
Is Device delivery system issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBUTEROL\BUDESONIDE. However, 244 reports have been filed with the FAERS database.
What Other Side Effects Does ALBUTEROL\BUDESONIDE Cause?
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)
Drug ineffective (62)
What Other Drugs Cause Device delivery system issue?
ALBUTEROL (9,509)
SOMATROPIN (1,848)
EXENATIDE (1,533)
BUDESONIDE\FORMOTEROL (1,260)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (1,181)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (523)
LEVALBUTEROL (459)
MOMETASONE FUROATE\OLOPATADINE (347)
ABATACEPT (342)
PEGFILGRASTIM (323)
Which ALBUTEROL\BUDESONIDE Alternatives Have Lower Device delivery system issue Risk?
ALBUTEROL\BUDESONIDE vs ALBUTEROL\IPRATROPIUM
ALBUTEROL\BUDESONIDE vs ALCAFTADINE
ALBUTEROL\BUDESONIDE vs ALCOHOL
ALBUTEROL\BUDESONIDE vs ALCOHOL\CHLORHEXIDINE
ALBUTEROL\BUDESONIDE vs ALDACTONE