Does ALBUTEROL Cause Product prescribing issue? 172 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 172 reports of Product prescribing issue have been filed in association with ALBUTEROL (Albuterol Sulfate). This represents 0.2% of all adverse event reports for ALBUTEROL.
172
Reports of Product prescribing issue with ALBUTEROL
0.2%
of all ALBUTEROL reports
0
Deaths
39
Hospitalizations
How Dangerous Is Product prescribing issue From ALBUTEROL?
Of the 172 reports, 39 (22.7%) required hospitalization, and 1 (0.6%) were considered life-threatening.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBUTEROL. However, 172 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 prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)
Which ALBUTEROL Alternatives Have Lower Product prescribing issue Risk?
ALBUTEROL vs ALBUTEROL\BUDESONIDE
ALBUTEROL vs ALBUTEROL\IPRATROPIUM
ALBUTEROL vs ALCAFTADINE
ALBUTEROL vs ALCOHOL
ALBUTEROL vs ALCOHOL\CHLORHEXIDINE