Does ALBUTEROL Cause Device use error? 5,215 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5,215 reports of Device use error have been filed in association with ALBUTEROL (Albuterol Sulfate). This represents 5.4% of all adverse event reports for ALBUTEROL.
5,215
Reports of Device use error with ALBUTEROL
5.4%
of all ALBUTEROL reports
3
Deaths
100
Hospitalizations
How Dangerous Is Device use error From ALBUTEROL?
Of the 5,215 reports, 3 (0.1%) resulted in death, 100 (1.9%) required hospitalization, and 5 (0.1%) were considered life-threatening.
Is Device use error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBUTEROL. However, 5,215 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 use error?
PEGFILGRASTIM (6,001)
ALBIGLUTIDE (4,056)
EVOLOCUMAB (4,002)
SOMATROPIN (2,801)
FLUTICASONE\SALMETEROL (1,749)
FLUTICASONE (783)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766)
ERENUMAB-AOOE (711)
ETANERCEPT (665)
TREPROSTINIL (563)
Which ALBUTEROL Alternatives Have Lower Device use error Risk?
ALBUTEROL vs ALBUTEROL\BUDESONIDE
ALBUTEROL vs ALBUTEROL\IPRATROPIUM
ALBUTEROL vs ALCAFTADINE
ALBUTEROL vs ALCOHOL
ALBUTEROL vs ALCOHOL\CHLORHEXIDINE