Does ALBUTEROL Cause Product dose omission issue? 2,714 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,714 reports of Product dose omission issue have been filed in association with ALBUTEROL (Albuterol Sulfate). This represents 2.8% of all adverse event reports for ALBUTEROL.
2,714
Reports of Product dose omission issue with ALBUTEROL
2.8%
of all ALBUTEROL reports
68
Deaths
396
Hospitalizations
How Dangerous Is Product dose omission issue From ALBUTEROL?
Of the 2,714 reports, 68 (2.5%) resulted in death, 396 (14.6%) required hospitalization, and 47 (1.7%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBUTEROL. However, 2,714 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 issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which ALBUTEROL Alternatives Have Lower Product dose omission issue Risk?
ALBUTEROL vs ALBUTEROL\BUDESONIDE
ALBUTEROL vs ALBUTEROL\IPRATROPIUM
ALBUTEROL vs ALCAFTADINE
ALBUTEROL vs ALCOHOL
ALBUTEROL vs ALCOHOL\CHLORHEXIDINE