Does LEVALBUTEROL Cause Product preparation error? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product preparation error have been filed in association with LEVALBUTEROL (Levalbuterol tartrate HFA inhalation). This represents 0.8% of all adverse event reports for LEVALBUTEROL.
11
Reports of Product preparation error with LEVALBUTEROL
0.8%
of all LEVALBUTEROL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product preparation error From LEVALBUTEROL?
Of the 11 reports.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVALBUTEROL. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does LEVALBUTEROL Cause?
Device delivery system issue (459)
Drug dose omission by device (395)
No adverse event (393)
Dyspnoea (224)
Drug ineffective (181)
Asthma (105)
Off label use (97)
Cough (70)
Device issue (68)
Incorrect dose administered by device (59)
What Other Drugs Cause Product preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBIGLUTIDE (691)
ALBUTEROL (520)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
LEUPROLIDE (400)
Which LEVALBUTEROL Alternatives Have Lower Product preparation error Risk?
LEVALBUTEROL vs LEVAMISOLE
LEVALBUTEROL vs LEVAQUIN
LEVALBUTEROL vs LEVEMIR
LEVALBUTEROL vs LEVETIRACETAM
LEVALBUTEROL vs LEVOBUNOLOL