Does ALBUTEROL Cause Device malfunction? 2,257 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,257 reports of Device malfunction have been filed in association with ALBUTEROL (Albuterol Sulfate). This represents 2.4% of all adverse event reports for ALBUTEROL.
2,257
Reports of Device malfunction with ALBUTEROL
2.4%
of all ALBUTEROL reports
3
Deaths
66
Hospitalizations
How Dangerous Is Device malfunction From ALBUTEROL?
Of the 2,257 reports, 3 (0.1%) resulted in death, 66 (2.9%) required hospitalization, and 33 (1.5%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBUTEROL. However, 2,257 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)
Device delivery system issue (9,509)
No adverse event (8,971)
Therapeutic product effect incomplete (8,496)
Cough (8,355)
Drug dose omission by device (8,162)
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)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
ACLIDINIUM (1,325)
Which ALBUTEROL Alternatives Have Lower Device malfunction Risk?
ALBUTEROL vs ALBUTEROL\BUDESONIDE
ALBUTEROL vs ALBUTEROL\IPRATROPIUM
ALBUTEROL vs ALCAFTADINE
ALBUTEROL vs ALCOHOL
ALBUTEROL vs ALCOHOL\CHLORHEXIDINE