Does ALBUTEROL Cause Device delivery system issue? 9,509 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9,509 reports of Device delivery system issue have been filed in association with ALBUTEROL (Albuterol Sulfate). This represents 9.9% of all adverse event reports for ALBUTEROL.
9,509
Reports of Device delivery system issue with ALBUTEROL
9.9%
of all ALBUTEROL reports
6
Deaths
114
Hospitalizations
How Dangerous Is Device delivery system issue From ALBUTEROL?
Of the 9,509 reports, 6 (0.1%) resulted in death, 114 (1.2%) required hospitalization, and 12 (0.1%) were considered life-threatening.
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. However, 9,509 reports have been filed with the FAERS database.
What Other Side Effects Does ALBUTEROL Cause?
Dyspnoea (21,856)
Asthma (18,997)
Wrong technique in product usage process (17,114)
Wheezing (11,555)
Drug ineffective (11,057)
No adverse event (8,971)
Therapeutic product effect incomplete (8,496)
Cough (8,355)
Drug dose omission by device (8,162)
Loss of personal independence in daily activities (6,920)
What Other Drugs Cause Device delivery system issue?
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)
ALBUTEROL\BUDESONIDE (244)
Which ALBUTEROL Alternatives Have Lower Device delivery system issue Risk?
ALBUTEROL vs ALBUTEROL\BUDESONIDE
ALBUTEROL vs ALBUTEROL\IPRATROPIUM
ALBUTEROL vs ALCAFTADINE
ALBUTEROL vs ALCOHOL
ALBUTEROL vs ALCOHOL\CHLORHEXIDINE