Does ALBUTEROL Cause Product preparation error? 520 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 520 reports of Product preparation error have been filed in association with ALBUTEROL (Albuterol Sulfate). This represents 0.5% of all adverse event reports for ALBUTEROL.
520
Reports of Product preparation error with ALBUTEROL
0.5%
of all ALBUTEROL reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product preparation error From ALBUTEROL?
Of the 520 reports, 3 (0.6%) required hospitalization.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBUTEROL. However, 520 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 preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBIGLUTIDE (691)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
LEUPROLIDE (400)
SODIUM OXYBATE (222)
Which ALBUTEROL Alternatives Have Lower Product preparation error Risk?
ALBUTEROL vs ALBUTEROL\BUDESONIDE
ALBUTEROL vs ALBUTEROL\IPRATROPIUM
ALBUTEROL vs ALCAFTADINE
ALBUTEROL vs ALCOHOL
ALBUTEROL vs ALCOHOL\CHLORHEXIDINE