Does ALBUTEROL Cause Product dose omission? 1,742 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,742 reports of Product dose omission have been filed in association with ALBUTEROL (Albuterol Sulfate). This represents 1.8% of all adverse event reports for ALBUTEROL.
1,742
Reports of Product dose omission with ALBUTEROL
1.8%
of all ALBUTEROL reports
3
Deaths
105
Hospitalizations
How Dangerous Is Product dose omission From ALBUTEROL?
Of the 1,742 reports, 3 (0.2%) resulted in death, 105 (6.0%) required hospitalization, and 3 (0.2%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBUTEROL. However, 1,742 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 Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
TOFACITINIB (1,104)
Which ALBUTEROL Alternatives Have Lower Product dose omission Risk?
ALBUTEROL vs ALBUTEROL\BUDESONIDE
ALBUTEROL vs ALBUTEROL\IPRATROPIUM
ALBUTEROL vs ALCAFTADINE
ALBUTEROL vs ALCOHOL
ALBUTEROL vs ALCOHOL\CHLORHEXIDINE